Abstract
Embryo implantation failures are a major challenge in reproductive medicine, but the underlying mechanism remains poorly understood. Successful implantation requires dynamic remodeling of the endometrium through integrated proliferation and differentiation of endometrial cells including luminal epithelial, glandular epithelial, and stromal cells. Conversely, their disruption causes infertility. Spatiotemporal control of transcription is required for these processes; however, the underlying epigenetic regulation is largely unknown. In this study, we examined expression data from the human endometrium during implantation and discovered that expression of the histone lysine methyltransferase KMT2D was significantly suppressed in patients with recurrent implantation failure. Further study revealed that uterine deletion of Kmt2d in mice caused infertility due to implantation failure. Morphological analysis discovered a reduction in the number of uterine glands and aberrant differentiation of the luminal and glandular epithelium into stratified phenotypes in Kmt2d knockout uteri. Administration of leukemia inhibitory factor protein, which is expressed in uterine glands and is essential for implantation, did not rescue implantation failure in Kmt2d knockout mice, suggesting that infertility was not solely due to uterine gland dysfunction. RNA sequencing analysis revealed that Kmt2d knockout uteri displayed suppressed expression of genes involved in ion homeostasis, which may affect the uterine luminal morphology. Our study suggests that KMT2D plays an essential role in facilitating successful embryo implantation by regulating the coordinated differentiation of endometrial cells, providing valuable insights into unexplained implantation failures in women.
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Introduction
Embryo implantation is the first important step for a successful pregnancy in mammals and requires bidirectional communication between the healthy blastocyst and receptive endometrium [1, 2]. The endometrium is a highly dynamic tissue undergoing molecular and cellular changes to transition into a receptive state for embryos during the menstrual cycle in human and the reproductive cycle in rodents. The receptive state is limited to a very short period in early pregnancy, which is called “the window of implantation” [1, 2]. Outside this window, the endometrium becomes refractory to embryos [3, 4]. In human fertility treatment, implantation failure occurs in approximately 60–70% of cases despite the transfer of high-quality embryos [5], presumably due to inadequate endometrial receptivity [6]. Therefore, understanding the regulation of endometrial receptivity is critical to improve the success rates of implantation in fertility treatment.
The endometrium, consisting of luminal and glandular epithelial cells as well as stromal cells, undergoes precise regulation of growth and differentiation by the ovarian steroid hormones estrogen (mainly 17β-estradiol, E2) and progesterone (P4) during establishment of receptivity [1, 2]. In mice, E2 from ovaries promotes epithelial cell proliferation on day 1 of pregnancy (defined as the day on which the vaginal plug is observed), followed by P4 from the newly formed corpora lutea inhibiting E2-induced cell division and promoting epithelial differentiation for embryo implantation [1, 2, 7]. On day 4 of pregnancy, a transient surge of E2 induces secretion of leukemia inhibitory factor (LIF) from uterine glands, initiating embryo attachment via LIF-LIFR-STAT3 signaling [8, 9]. Upon embryo attachment, endometrial stromal cells surrounding the embryo terminally differentiate into decidual cells, supporting subsequent trophoblast invasion and placentation [10]. Imbalance in hormonal signaling disrupts endometrial tissue integrity, leading to implantation failure and infertility [11]. Moreover, improper tissue development in the endometrium, such as uterine gland deficiency or abnormal stratification of epithelium, is known to affect receptivity [12,13,14,15].
Dynamic tissue remodeling in the peri-implantation endometrium is manifested by spatiotemporal regulation of gene expression in endometrial cells. Epigenetic machinery, which alters chromatin structure and transcription through DNA/RNA methylation and histone modification, may be the basis of precise transcriptional regulation in the endometrium. Recent studies using mouse models have shown that defects of several epigenetic modifiers in the uterus lead to infertility due to abnormal transcription in endometrial cells [16,17,18,19,20,21,22,23,24], shedding light on the involvement of epigenetics in endometrial functions. Cell- and tissue-specific gene expression relies on enhancers, which are cis-regulatory regions containing transcription factor-binding sites [25, 26]. Enhancers are located far from transcription start sites of genes, and these regions are epigenetically marked by mono-methylation of histone H3 lysine 4 (H3K4me1) [25, 26]. In mammals, enhancer-associated H3K4me1 is mainly catalyzed by the histone lysine methyltransferases KMT2C and KMT2D (also known as MLL3 and MLL4, respectively) with partially redundancy [27]. KMT2C/D are important for precise regulation of H3K4me1 levels at enhancer regions and cell-specific transcription [28, 29]. Genetic mutations in KMT2C/D are primary causes of neurodevelopmental disorders, such as Kleefstra syndrome 2 and Kabuki syndrome, respectively [30,31,32]. Moreover, somatic mutations in KMT2C/D have been found in many types of cancer including endometrial cancer, indicating these genes are involved in tissue homeostasis and tumorigenesis [33,34,35]. Although the links between KMT2s and several diseases are becoming clear, the importance of KMT2C/D for tissue development and homeostasis of reproductive organs is largely unknown.
Here, we found that KMT2D expression was decreased in patients with recurrent implantation failure (RIF). To explore the role of KMT2D in the endometrium, we deleted Kmt2d in murine uterus and showed that Kmt2d is indispensable for successful embryo implantation. Kmt2d deficiency induced morphological abnormalities in the uterus, including a reduced uterine gland and abnormal epithelium differentiation, which impaired endometrial receptivity. Our findings not only reveal that KMT2D plays a critical role in regulation of uterine morphology and function in mice, but also suggest that KMT2D suppression may influence unexplained implantation failures in human patients.
Results
Expression of KMT2 genes is decreased in the endometrium of patients with RIF
A prior study using RNA-seq data from the human endometrium during implantation found that downregulation of epigenetic factors like EZH1/2 and EEH in patients with RIF [20]. Using the same dataset, we further examined the expression of genes involved in enhancer activity, KMT2C and KMT2D, in RIF patients. Comparison of the reads per kilobase of transcript per million mapped reads (RPKM) values of KMT2 genes between fertile control and RIF patients revealed that KMT2D expression was significantly decreased in RIF patients, but KMT2C expression was not (Fig. 1a). Moreover, KMT2A and KMT2B, which code enzymes for di- and tri-methylation of H3K4 [27], were also downregulated in RIF patients (Fig. 1b). A heatmap of KMT2 gene expression showed that samples with low KMT2D expression also had low expression of other KMT2 genes (Fig. 1c). Indeed, the RPKM value of KMT2D correlated well with other KMT2 genes in human endometrium (R2 = 0.7802 vs. KMT2A, R2 = 0.5576 vs. KMT2B, and R2 = 0.7774 vs. KMT2C). Our analysis demonstrated that expression of KMT2 genes was concomitantly decreased in the endometrium of RIF patients.
Uterine deletion of Kmt2d in mice caused infertility due to implantation failure
KMT2D downregulation in the endometrium of RIF patients suggested a critical role of KMT2D during implantation. To investigate the roles of KMT2D in the uterus, we generated mice with conditional knockout of Kmt2d in the uterus by crossing Kmt2d-floxed (Kmt2df/f) mice with PgrCre mice [24], which expressed Cre recombinase in the uterus. Uterine deletion of Kmt2d (PgrCre, Kmt2df/f; hereafter described as Kmt2dd/d) was confirmed in DNA (Fig. 2a, b), and mRNA levels (Fig. 2c). Female fertility was assessed by paring Kmt2dd/d or Kmt2df/f female (as control) mice with wild-type male for 6 months, and litters and pups were tracked. While all control mice produced pups, Kmt2dd/d females did not become pregnant and give birth (Fig. 2d). Next, we analyzed whether Kmt2d ablation affected implantation. By the evening on day 5 of pregnancy, Kmt2df/f uteri showed apparent implantation sites, but no implantation sites were observed in Kmt2dd/d uteri (Fig. 2e). Histological analysis indicated that embryos were implanted in the endometrium, tightly contacted with closed lumen, and surrounded by decidua in Kmt2df/f uteri (Fig. 2f, left). Conversely, in Kmt2dd/d uteri, embryos lay on the uterine luminal epithelium with the endometrial lumen remaining open (Fig. 2f, right), indicating implantation was compromised. Expression of PTGS2, a key enzyme for prostaglandin synthesis (also known as COX2), was detected in the stroma surrounding the embryo in control uteri on day 5 (Fig. 2g), indicating successful embryo attachment [36, 37]. By contrast, PTGS2 expression was mainly detected on the epithelium surrounding the embryo in Kmt2dd/d uteri (Fig. 2g). This resembles the patterns observed in Lif−/− and Msx1/2d/d mice, which are infertile due to implantation failure [38, 39], suggesting impaired implantation in Kmt2dd/d uteri.
a The strategy to conditionally delete the Kmt2d gene. P1–3 indicate the locations of primers used for genotyping. b Genotyping PCR results showing Kmt2d was deleted in the uterus. T, tail DNA; Ut, uterus DNA; NC, negative control (water). c Decreased expression of Kmt2d gene in Kmt2dd/d uteri was confirmed by RT-qPCR analysis. d The results of a 6-month breeding assay. The numbers of deliveries (left) and total pups (right) were lower for Kmt2dd/d mice than for Kmt2df/f mice. n = 4 per group. P-values were calculated with the two-tailed Mann–Whitney U test. e Representative images of the gross anatomy of uteri on day 5 of pregnancy in control (left) and Kmt2dd/d (right) mice. Implantation sites were visualized by injected blue dye in Kmt2df/f uteri, but not in Kmt2dd/d uteri. Scale bar = 10 mm. f Cross-sections of implantation sites on day 5 of pregnancy. Insets show embryos (red arrowheads) in the uterine cavity. The uterine lumen in Kmt2df/f mice was tightly closed to contact with embryos, but Kmt2dd/d uteri displayed a space within the lumen due to abnormal closure. Luminal spaces are indicated by blue double-headed arrows. Scale bars indicate 250 μm (low magnification images) and 100 μm (insets). g Immunohistochemistry of PTGS2 in day 5 uteri of Kmt2df/f and Kmt2dd/d mice. In the Kmt2df/f uterus, PTGS2 expression (black arrows) was observed in stroma around the implantation site (IS) but was absent in the non-IS. PTGS2 expression in the Kmt2dd/d uterus was mainly detected in the epithelium around the embryo (the embryo is indicated by a red arrowhead). Scale bar = 100 μm. h Representative images showing the gross anatomy of the oil-injected (arrowhead, right horn) and untreated (left horn) uterine horns of Kmt2df/f and Kmt2dd/d females at 3 days after oil injection. Scale bar = 10 mm. i The ratio of the weight of the oil-injected uterine horn (n = 4) to that of the untreated uterine horn (n = 4). The P-value was calculated using the two-tailed Mann-Whitney U test.
Kmt2dd/d uteri showed no signs of decidua on day 5; therefore, we next examined whether Kmt2d ablation impacts decidualization in the uterus using an artificial model [40]. Sesame oil was injected into uteri of pseudopregnant mice and decidualization was examined 2 days later. Kmt2df/f uteri exhibited a clear decidual response (Fig. 2h, left). However, Kmt2dd/d uteri did not form decidua after oil injection (Fig. 2h, right). The stimulated uterine horn of Kmt2dd/d mice weighed less than that of Kmt2df/f mice (Fig. 2i), indicating impaired decidualization in Kmt2dd/d uteri.
The phenotypes of ovaries in Kmt2dd/d mice were also examined, but we did not find any histological abnormality compared with ovaries of Kmt2df/f mice (Fig. S1a). Serum levels of E2 and P4 on day 4 of pregnancy were also comparable (Fig. S1b). Thus, we concluded that infertility of these mice was due to abnormal uterine functions.
KMT2C is a paralog of KMT2D and they share several functional redundancies [27]; therefore, we examined the role of KMT2C in the uterus using Kmt2c knockout females (PgrCre, Kmt2cf/f; hereafter described as Kmt2cd/d, Fig. S2a, b). Kmt2cd/d females had normal pregnancies from embryo implantation (Fig. S2c) to parturition (Fig. S2d). Kmt2c deletion did not have apparent effects on female fertility; therefore, subsequent analyses focused on Kmt2d.
Kmt2d ablation alters responsive signaling in the uterine epithelium
Next, we examined whether Kmt2d ablation affected the molecular status of endometrial receptivity. The implantation window in the mouse uterus occurs on day 4 of pregnancy, during which the endometrium transitions from an E2-dominant state to a P4-responsive state [1, 2]. Dysregulation of hormonal signaling in the endometrium affected receptivity [11]; therefore, we analyzed E2- and P4-responsive gene expression in Kmt2dd/d uteri on day 4 of pregnancy. Among E2-responsive genes, whose expression is normally suppressed on day 4 of murine pregnancy, Ltf was significantly upregulated in Kmt2dd/d uteri, while Muc1 and Wnt5a expressions were comparable in Kmt2dd/d and Kmt2df/f uteri (Fig. 3a). Ihh, an epithelial P4-targeted gene, was markedly downregulated in Kmt2dd/d uteri (Fig. 3a). Another epithelial P4-targeted gene, Areg, was not altered in Kmt2dd/d uteri. Expression of stromal P4-responsive genes such as Hand2 and Il13ra2 remained unchanged (Fig. 3a). Expression of hormone receptors including Esr1 and Pgr was not altered in Kmt2dd/d uteri (Fig. 3a). These data suggested that Kmt2d ablation altered hormone-responsive signaling, especially in the uterine epithelium.
a Expression analysis of E2- and P4-responsive genes by RT-qPCR. n = 3 and 5 in Kmt2df/f and Kmt2dd/d, respectively. *p < 0.05, two-tailed Mann–Whitney U test. b Cell proliferation in uteri on day 4 of pregnancy determined by immunohistochemistry of the cell proliferation marker Ki67. LE luminal epithelium, GE glandular epithelium, St stroma. Scale bar = 50 μm. c Percentages of Ki67-positive luminal epithelial cells (left) and stromal cells (right). *p < 0.05, two-tailed Mann–Whitney U test.
Epithelial proliferation during implantation is inhibited in Kmt2d d/d uteri
During implantation in mouse, increased P4 signaling terminates proliferation of endometrial epithelial cells and increases the proliferation activity of stromal cells [4]. RT-qPCR analysis showed that P4 signaling was inhibited in the Kmt2dd/d uterine epithelium on day 4 of pregnancy (Fig. 3a); therefore, we expected epithelial proliferation to be aberrantly upregulated in Kmt2dd/d uteri. Immunostaining of Ki67, a marker of proliferating cells, was performed to identify proliferation status. In Kmt2df/f uteri, Ki67-positive cells were rarely observed in the epithelium as previously reported (Fig. 3b, left). Unexpectedly, epithelial proliferation was also inhibited in Kmt2dd/d uteri (Fig. 3b, right, and Fig. 3c). On the other hand, the Ki67-positive proliferating cells in the stroma were increased in Kmt2dd/d uteri (Fig. 3c). Epithelial proliferation was apparent in estrus and on day 1 of pregnancy in both Kmt2df/f and Kmt2dd/d uteri (Fig. S3). These results suggested that inhibition of epithelial proliferation during implantation was correctly controlled in Kmt2dd/d uteri despite abnormal ovarian hormonal signaling in Kmt2dd/d endometrium.
Kmt2d is crucial for precise development of uterine glands
During histological observations, we found that Kmt2dd/d uteri had fewer uterine glands than control uteri. Immunohistochemistry for FOXA2, a marker of uterine glandular epithelial cells, confirmed that the FOXA2-positive uterine glands were reduced in Kmt2dd/d uteri during implantation (Fig. 4a, b) and in non-pregnancy (Fig. 4c). Uteri were visualized in 3D by correlative microscopy and block-face imaging to confirm these results of 2D histological observation (Fig. S4, and Movies S1, S2) [41]. The 3D morphological data confirmed the reduction of uterine glands at the whole-tissue level. Notably, a reduction in FOXA2-positive gland cells was already observed in the developing uterus (postnatal day 14, Fig. S5). These observations revealed that Kmt2d is essential for precise development of uterine glands.
a Immunohistochemistry for FOXA2, a marker of endometrial glandular epithelial cells, in the uterus on day 4 of pregnancy. The number of FOXA2-positive glandular ducts per cross-section of the uterus on day 4 of pregnancy (b) and of the non-pregnant uterus in diestrus c. At least three females were analyzed per group. d Expression of genes related to LIF signaling in day 4 uteri examined by RT-qPCR. n = 3 and 5 in Kmt2df/f and Kmt2dd/d, respectively. *p < 0.05, two-tailed Mann–Whitney U test. e–g Rescue experiment of implantation failure by LIF supplementation. e Black arrowheads indicate implantation sites on day 6 of a normal pregnancy in a wild-type C57BL/6J female mouse. Scale = 10 mm. f Treatment with recombinant LIF induced implantation in a delayed implantation model using wild-type female mice. g Implantation sites were not observed in Kmt2dd/d uteri at 2 days after supplementation of recombinant LIF on day 4 of pregnancy. Histology and immunolocalization of p63, a marker of basal cells in the stratified epithelium, in adult (h, day 4 of pregnancy) and developing (i, postnatal day 14) uteri. p63-positive cells (black arrows) were present in Kmt2dd/d uteri, but not in Kmt2df/f uteri. Scale bar = 100 μm.
Recombinant LIF does not rescue implantation failure in Kmt2d d/d females
The primary function of uterine glands during implantation is to secrete LIF, an essential cytokine for initiation of implantation [8]. To examine whether reduction of glands in Kmt2dd/d uteri leads to insufficiency of LIF, we assessed the expressions of Lif and its downstream genes in the uterus during implantation. The diminished Foxa2 expression in Kmt2dd/d uteri confirmed reduced gland number in Kmt2dd/d uteri (Fig. 4d). Lif and downstream Coch were significantly downregulated in Kmt2dd/d uteri, although expression of another downstream gene, Igfbp3, was comparable in Kmt2df/f and Kmt2dd/d uteri (Fig. 4d). These findings indicated that LIF signaling was compromised in Kmt2dd/d uteri during implantation.
A previous study reported that administration of recombinant LIF rescues implantation failure in gland-deficient mice [42]. We examined whether the implantation failure in Kmt2dd/d mice was also rescued by LIF administration. In normal pregnancies of wild-type females, implantation sites were apparent on day 6 of pregnancy (Fig. 4e). Administration of recombinant LIF protein effectively induced implantation in delayed implantation model mice, confirming its biological activity (Fig. 4f). However, LIF administration on day 4 did not induce implantation in Kmt2dd/d females (Fig. 4g, n = 3). These findings indicated that implantation failure in Kmt2dd/d mice was not solely due to dysfunction of uterine glands.
A stratified epithelium appears in Kmt2d d/d uteri
We also identified that some glandular structures exhibited a stratified morphology in Kmt2dd/d uteri (Fig. 4a, white arrowhead). Immunostaining for p63, a marker of stratified basal cells, confirmed that p63-positive basal cells were present in the luminal and glandular epithelium in adult Kmt2dd/d uteri, but were completely absent in control uteri (Fig. 4h). p63-positive cells had already appeared in the developing uterus on postnatal day 14 in Kmt2dd/d females (Fig. 4i). These results suggested that Kmt2d plays a pivotal role in the development programs of the endometrial epithelium.
Genes related to ion homeostasis are downregulated in Kmt2d d/d uteri
To further explore the cause of infertility in Kmt2dd/d mice, we conducted RNA-seq analysis on day 4 of pregnancy. We identified that 283 and 477 genes were upregulated and downregulated in Kmt2dd/d uteri, respectively (Fig. 5a and Dataset S1). Gene ontology analysis revealed that upregulated genes in Kmt2dd/d uteri were highly enriched in “Keratinocyte differentiation” (Fig. 5b). Keratinocytes are the major cell type in the stratified skin epidermis, consistent with our observation that stratified epithelium appeared in Kmt2dd/d uteri. Downregulated genes were enriched in “Homeostasis” and “Cell migration” (Fig. 5c). In “Homeostatic process”, 74 genes were downregulated, including 39 genes related to “Ion homeostasis”, such as those encoding sodium ion (Scn1b, Scn3b, and Scn7a) and potassium ion (Kcna5) channels (Fig. 5d). Given that regulation of ion homeostasis in the uterine lumen is essential for precise uterine function [43,44,45], our data suggested that an imbalance of ion homeostasis underlies the infertility of Kmt2dd/d females.
a A volcano plot showing gene expression profiles determined by RNA-seq. DEGs (q < 0.05 and fold change >2) between Kmt2df/f and Kmt2dd/d uteri on day 4 of pregnancy are illustrated in red. Enriched biological processes in upregulated (b) and downregulated (c) DEGs. d Heatmap of expression of DEGs related to the term “Homeostatic process” from RNA-seq data. e Graphical summary of the findings about implantation failure in the Kmt2dd/d mouse model.
Given the resemblance of the hypo-development of uterine glands in Kmt2dd/d mice to Foxa2d/d mice, we compared the transcriptomes of these two strains using a published RNA-seq dataset (GSE113065). Downregulated genes in Foxa2d/d uteri on day 4 also exhibited lower expression levels in Kmt2dd/d uteri (Fig. S6). This observation suggested that KMT2D and FOXA2 regulate common gene sets in the murine endometrium.
Our mouse model reveals the critical roles of KMT2D in precise differentiation of endometrial cells and successful implantation. Ablation of Kmt2d in murine uterus resulted in infertility due to implantation failure, accompanied by uterine gland hypo-development and abnormal stratified differentiation of the uterine epithelium (Fig. 5e). Kmt2d ablation also altered transcriptome programs in the endometrium, as exemplified by downregulation of genes related to ion homeostasis. Thus, we propose that KMT2D regulates multiple layers of functions for successful implantation in the endometrium, and Kmt2d deficiency has serious consequences for female fertility.
Discussion
The KMT2 family consists of highly conserved proteins, which has a catalytic SET domain that methylates lysine residues of histone H3 [28]. Among them, KMT2C and KMT2D share a common ancestral homolog, Drosophila Trithorax-related (Trr), which regulates enhancer activity by catalyzing mono-methylation of H3K4 to the target regions [46]. KMT2C/D have highly similar protein structures and therefore share some level of redundant functions [27, 29]. However, systemic knockout of Kmt2c or Kmt2d in mice results in embryonic lethality at different stages [47], suggesting that the importance of KMT2C/D for mammalian development is not equivalent and varies according to the stage and tissue. In this study, we found that expression of KMT2D, but not KMT2C, was downregulated in the endometrium of patients with RIF (Fig. 1). Consistent with expression data from patient samples, our mouse model revealed that deletion of Kmt2d in uterus led to female infertility due to implantation failure (Fig. 2), but knockout of Kmt2c did not. Thus, Kmt2d appears to be more important than Kmt2c for uterine development and function. Somatic mutations of KMT2D are found more frequently than KMT2C mutations in human endometrial cancer [35], indicating the tissue-specific importance of KMT2 genes. KMT2D mutations have also been observed in Kabuki syndrome patients. However, these patients (both male and female) appear to be fertile [48], suggesting that haploinsufficiency of KMT2D does not significantly affect uterine function. We found that other KMT2 genes in addition to KMT2D were simultaneously downregulated in the endometrium of RIF patients; therefore, suppression of multiple KMT2 genes may distort epigenetic regulation in the endometrium, resulting in implantation failure. Indeed, it was reported that KMT2B can compensate for the enhancer activity regulated by KMT2C/KMT2D [49]. A future study needs to identify the cause of simultaneous suppression of KMT2 genes in the endometrium of RIF patients.
Epithelial proliferation in the endometrium is inhibited during murine implantation, which is a hallmark of a receptive uterus, whereas stromal cells increase their growth [4]. These states are both achieved by increased P4-PGR signaling in the endometrium at the time of implantation [50]. Intriguingly, the proliferation of stromal cells in Kmt2dd/d endometrium was more pronounced than in control mice (Fig. 3c), but no abnormal enhancement of P4-PGR signaling was observed in the Kmt2dd/d uteri (Fig. 3a, and Fig. S1). Thus, the increased proliferation in stromal cells may not be due to dependent on P4-PGR signaling, but rather other causes. Although it is not clear whether the increased stromal proliferation itself is a direct cause of implantation failure in Kmt2dd/d mice, we observed evidence indicating abnormalities in the characteristics of stromal cells in the knockout mice. PTGS2 (COX2) expression typically propagates from the epithelium to the stroma during implantation, but this propagation is scarcely observed in the knockout uterus (Fig. 2g). Additionally, stromal cells differentiate into decidual cells that support fetal growth, but there is no decidualization in the uteri of Kmt2dd/d mice (Fig. 2f and g). These abnormalities in uterine stromal cells may partially contribute to the implantation defect in Kmt2dd/d mice.
The prominent phenotype of Kmt2dd/d uteri was endometrial gland reduction. Uterine gland development (i.e., adenogenesis) begins after birth in mice and is completed by 3 weeks of age [51]. Foxa2 is the master regulator of uterine adenogenesis because mice lacking Foxa2 in the uterus shortly after birth suffer from uterine gland aplasia [14]. FOX family transcription factors, including FOXA2, are pioneer factors that open up compacted chromatin by preferentially binding to heterochromatin regions during cell differentiation, contributing to formation of cell-specific enhancers and subsequent gene expression in post-differentiated cells [52, 53]. In the colon, binding of FOXD2 to compacted chromatin facilitates recruitment of KMT2D and rewiring enhancer through deposition of H3K4me1, which functions as a tumor suppressor [54]. Although Foxa2 expression was decreased in Kmt2dd/d uteri, this may reflect the reduced number of uterine glands. Instead, loss of Kmt2d may disrupt formation of FOXA2-regulated enhancers, leading to defective development of uterine glands in Kmt2dd/d females. Our observation that downregulated genes in Foxa2d/d uteri also exhibited lower expression levels in Kmt2dd/d uteri supports the idea that Kmt2d and Foxa2 operate in the same regulatory pathway for glandular development in the murine endometrium (Fig. S6).
Implantation failure in mice lacking uterine glands due to Foxa2 deletion is rescued by LIF supplementation [42], demonstrating that the most critical role of uterine glands during murine implantation is to secrete LIF. Although Kmt2dd/d mice also exhibited fewer uterine glands, LIF administration alone did not rescue implantation failure (Fig. 4g), suggesting that endometrial receptivity in Kmt2dd/d mice is disrupted at a stage before LIF action. While we failed to detect abnormal receptivity in Kmt2dd/d uteri in terms of inhibition of epithelial proliferation, Kmt2dd/d uteri may lack other factors necessary for embryo implantation, such as protein secretion or expression of adhesion molecules in the luminal epithelium. Further experiments are required to elucidate why LIF administration does not rescue implantation failure in Kmt2dd/d mice.
Stratification of the uterine epithelium was apparent in Kmt2dd/d uteri. During development of female reproductive ducts, the Müllerian duct epithelium in the fetus becomes a monolayer of uterine epithelial cells or stratified vaginal epithelial cells dependent on paracrine factors released by stromal cells, such as bone morphogenetic proteins (BMPs) and fibroblast growth factors (FGFs) [55, 56]. The stratified epithelium is completely absent in the normal uterus in rodents and human, but appears in pathological conditions such as endometrial cancer [57, 58]. Abnormal stratification is also observed in uteri of several genetically modified mice, such as strains with knockout of Fgfr2 and Wnt4 [15, 59]. In Kmt2dd/d uteri, expression of several genes related to the BMP, FGF, and WNT pathways was abnormal compared with control (Fig. S7). Disrupted paracrine signaling likely alters the epithelial differentiation program, resulting in abnormal stratification of the uterine epithelium in Kmt2dd/d uteri. In the epithelium, a morphological difference (i.e., single layer or stratified) reflects functional differences; thus, several epithelial functions, including protein secretion and absorption, are impaired in Kmt2dd/d uteri, resulting in abnormal receptivity.
As described above, Kmt2dd/d females exhibited significant morphological abnormalities in the uterus. Since the public human data used for the RNA-seq analysis excluded patients with known uterine abnormalities [20], it is likely that no known uterine morphological abnormalities occur in the uteri of patients with RIF in which KMT2D suppression is present. Possible explanations for the discrepancy between human patients and the mouse model regarding uterine morphological abnormalities include the following: (1) In the patient’s uterus, unlike in the knockout model, KMT2D expression was not completely abolished, resulting in functional but not morphological abnormalities. (2) In the mouse model, KMT2D knockout begins soon after birth, leading to uterine developmental abnormalities (see Fig. 4i, and Fig. S5), whereas in the human patient’s uterus, the reduction in KMT2D expression may be an acquired event (i.e., occurring in adulthood) and not accompanied by uterine morphological abnormalities. Future work is needed to generate and validate a model in which KMT2D knockout occurs in the uterus after sexual maturation.
Transcriptome analysis of peri-implantation uteri revealed that Kmt2d ablation decreased expression of genes related to homeostasis, especially ion homeostasis. Absorption and secretion of ions such as sodium and chloride ions in the luminal epithelium regulate fluid volumes in the endometrial lumen through osmotic pressure [43,44,45]. Mechanistically, active sodium ion uptake drives fluid absorption from the lumen into the blood, while chloride ion secretion drives fluid movement from the blood into the lumen, concomitant with sodium ion secretion [43, 45]. At the time of implantation, the uterine lumen must close tightly in contact with the embryo (Fig. 2f, left panel, and Fig. 5e), a process that is supposedly mediated by absorption of luminal fluid in the uterine epithelium [60]. By contrast, the lumen did not close at the time of implantation in Kmt2dd/d uteri (Fig. 2f, right panel, and Fig. 5e). Improper control of ion concentrations in the uterine lumen may result in retention of uterine luminal fluid, causing failure of luminal closure in Kmt2dd/d uteri. Furthermore, suppression of epithelial sodium ion channels in the murine uterus triggers implantation failure via inhibition of prostaglandin E2 release and decidualization defects [44]. Thus, ion homeostasis in the uterus is involved in protection of successful implantation in multiple respects.
The DEGs involved in “ion homeostasis”, which were reduced in Kmt2dd/d mice, also included genes encoding voltage-gated sodium channels, such as Scn1b, Scn3b, and Scn7a (Fig. 5d), which are primarily expressed in muscle and nerve cells. Recent studies have demonstrated that functional voltage-gated sodium channels are expressed in non-excitable cells, including mammary epithelial cells [61], retinal pigment cells [62], and macrophages [63]. These genes play roles in cell adhesion and phagocytosis [61,62,63]. Therefore, the voltage-gated sodium channel genes downregulated in Kmt2dd/d mice may also be involved in the regulation of embryo implantation via ion homeostasis through non-canonical functions. Another possible explanation is that since RNA-seq is performed using RNA extracted from the whole uterus, uterine smooth muscle contraction or dysregulation of neural activity, which is sparsely present in the uterus, may influence implantation failure.
In summary, we revealed that KMT2D plays a critical role in embryo implantation through precise regulation of uterine development and homeostasis in mice. Recent studies using animal models revealed that other histone modifiers such as EZH2, CFP1, and HDAC3 also have indispensable roles in maintaining uterine transcriptome networks to prepare the endometrium for embryo implantation [16,17,18, 20, 21, 64, 65]. Our results enhance understanding of epigenetic regulation in the endometrium and are expected to pave the way for future advancements in the diagnosis and treatment of unexplained implantation defects.
Materials and methods
Animal experiments
C57BL/6J and ICR mice were obtained from Charles River Japan (Yokohama, Japan). B6D2F1 mice were purchased from CLEA Japan (Kawasaki, Japan). All mice were housed in a specific pathogen-free facility with a 12 h dark/light cycle, and were chosen randomly without blinding. All animal studies were approved by the Animal Care and Experimentation Committee of Gunma University (approved No. 23-048) and were carried out in accordance with approved guidelines.
For implantation analysis, females were crossed with a wild-type male in the same cage. Day 1 of pregnancy was defined as the day on which the vaginal plug was identified. Implantation sites were visualized by intravenous injection of 2% Evans blue dye dissolved in phosphate-buffered saline (PBS) at 17:00 on day 5 of pregnancy. When uterine tissues were harvested on day 4 of pregnancy, blastocysts were recovered by flushing the uterine horns with PBS to evaluate embryo development prior to implantation. Uteri from which blastocysts were not recovered were not used in subsequent experiments. For the breeding assay, mature females (>7 weeks old) were mated with wild-type C57BL/6J males over 6 months. The numbers of litters and pups were recorded.
Generation of uterine-specific Kmt2c/Kmt2d conditional knockout mice
Kmt2c- and Kmt2d-floxed mice (Kmt2cf/f and Kmt2df/f) were generated using an electroporation method as previously reported [66]. Single-stranded donor oligodeoxynucleotides (ssODNs) with 5′- and 3′-homology arms corresponding to target sequences, flanking loxP, and containing a restriction site were designed (Fig. 1a and SI Appendix, Fig. S1a). Opti-MEM I (Life Technologies, Carlsbad, CA) containing pre-annealed crRNA/tracrRNA (3 μM), recombinant Cas9 protein (100 ng μl−1; GeneArt Platinum Cas9 nuclease; Thermo Fisher Scientific, Waltham, MA), and ssODN (400 ng μl−1; Ultramer; Integrated DNA Technologies, Coralville, IA) was used as the electroporation medium. A left loxP site was introduced into the intron between exons 8 and 9 of Kmt2c for Kmt2cf/f or exons 15 and 16 of Kmt2d for Kmt2df/f by electroporation using C57BL/6J-derived zygotes, and then edited embryos were transferred to the oviduct of a pseudopregnant ICR female mouse to obtain males with one loxP site in the left region. Next, a right loxP site was inserted into the intron between exons 13 and 14 of Kmt2c or exons 19 and 20 of Kmt2d by genome editing using left loxP site-containing male-derived zygotes to obtain Kmt2c- and Kmt2d-floxed mice. Sequence information of the crRNAs and ssODNs is provided in Table S1. Uterine-specific Kmt2c and Kmt2d knockout mice (Kmt2cd/d and Kmt2dd/d) were established by several crossings of the PgrCre strain [24] with floxed mice. Floxed females in the same litters as knockout animals were used as controls unless otherwise noted. The primers used for PCR analysis to assess uterine-specific deletion of Kmt2c and Kmt2d are listed in Table S2.
Histology
Collected murine tissues were fixed in PBS (pH 7.4) containing 4% paraformaldehyde and embedded in paraffin blocks. For histological analysis, sections (3 μm) were stained with hematoxylin and eosin (H&E). For immunohistochemistry, the sections were deparaffinized and incubated in 10 mM sodium citrate buffer (pH 6.0) at 121 °C for 5 min for antigen retrieval. The sections were further incubated with 3% hydrogen peroxide diluted with methanol for 15 min. After incubation with blocking buffer (PBS containing 10% goat serum, 1% bovine serum albumin, and 0.05% Tween 20), the sections were reacted with primary antibodies against PTGS2 (66351-1-Ig; Proteintech, Rosemont, IL), Ki67 (ab15580; Abcam, Cambridge, UK), FOXA2 (ab108422, Abcam), and p63 (ab124762, Abcam). The sections were then reacted with Histofine Simple Stain MAX-PO (Nichirei, Tokyo, Japan). Signals were developed with 3-3′-diaminobenzidine, followed by counterstaining with hematoxylin.
Artificial decidualization test
The artificial decidualization test was performed by intra-luminally injecting 0.02 mL of sesame oil into pseudo-pregnant female mice at 12:00 on day 4 of pseudo-pregnancy. These mice were generated by mating with a vasectomized male as previously described [40]. The uterine horns were dissected 2 days after oil injection and weighed.
Reverse transcription-quantitative PCR (RT-qPCR) analysis
Uteri on day 4 of pregnancy were harvested and kept at −80 °C until RNA extraction. Total RNA was isolated from uterine tissues using TRIzol reagent (Invitrogen, Carlsbad, CA). Following DNase I treatment and RNA purification using a FastGene RNA Premium Kit (Nippon Genetics, Tokyo, Japan), cDNA was synthesized using SuperScript II (Invitrogen) with random primers. RT-qPCR was performed using a LightCycler 96 system (Roche, Basel, Switzerland) with TB Green Premix Ex Taq II (Takara). Gene expression levels were calculated using the standard curve method and normalized to those of the ribosomal protein gene Rplp0. The primers used for RT-qPCR analysis are provided in Table S2.
Correlative microscopy and block-face imaging (CoMBI)
Three-dimensional reconstructed images of uteri were created by a CoMBI system (https://combi-3d.github.io/manual/) [41]. Briefly, fixed uteri were stained with PBS containing 1% tannic acid overnight, immersed in PBS containing 30% sucrose, and frozen. The tissue blocks were sliced at a thickness of 5 µm using a Leica CM3050S cryostat (Leica Microsystems K.K., Tokyo, Japan) at -20°C. Serial block-face images were captured using a digital camera (Sony a7RIII, Tokyo, Japan), a macro lens (Sigma APO MACRO 180 mm F2.8 EX DG OS HSM, Tokyo, Japan), and a teleconverter (Kenko HD pro 2x, Tokyo, Japan). Camera shutter release was regulated with CoMBI devices composed of a magnetic sensor and microcontroller. Images were processed using ImageJ, ilastik [67], and 3D Slicer [68]. A few sections were also collected and correlated with the block-face images to identify structures.
ELISAs of serum hormone levels
Blood samples were collected from females on day 4 of pregnancy, centrifuged (5000 × g for 10 min at 4 °C) to collect serum, and stored at −80 °C. The serum concentrations of 17β-estradiol and progesterone were estimated using an estradiol ELISA kit (cat# 501890; Cayman, Ann Arbor, MI) and a progesterone ELISA kit (cat# 582601, Cayman), respectively.
Rescue experiment of implantation failure by recombinant leukemia inhibitory factor (LIF) administration
Pregnant Kmt2dd/d females were intraperitoneally injected with 10 μg of recombinant mouse LIF (BioLegend, San Diego, CA) at 10:00 and 18:00 on day 4 of pregnancy, as described previously [42]. Implantation sites were evaluated at 18:00 on day 6 of pregnancy. The efficiency of recombinant LIF was verified using a delayed implantation model mice, as we previously reported with minor modifications [4]. Briefly, delayed implantation was induced by ovariectomizing pregnant C57BL/6J females at 17:00 on day 3 of pregnancy and was maintained by daily subcutaneous injection of progesterone (1 mg per mice). Two days after ovariectomy, recombinant LIF was intraperitoneally administered to induce implantation. Implantation sites were evaluated 2 days after LIF administration.
Library preparation for RNA sequencing (RNA-seq)
Total RNA was isolated from uteri on day 4 using TRIzol reagent and purified using an RNeasy Mini Kit (Qiagen Inc., Hilden, Germany) after treatment with DNase. mRNA was purified with Oligo dT beads (NEBNext Poly (A) mRNA magnet Isolation Module; New England Biolabs (NEB), Ipswich, MA), and cDNA libraries were produced with a NEBNext Ultra II RNA Library Prep Kit (NEB) and NEBNext Multiplex Oligos (NEB) as described previously [69]. The quality and concentration of libraries were confirmed using an Agilent 2200 TapeStation (D1000; Agilent, Santa Clara, CA). Libraries combined at equal molecular amounts were analyzed on an Illumina Nova-seq6000 DNA sequencer with a 50 bp paired-end cycle sequencing kit (Illumina Inc., San Diego, CA).
Analysis of RNA-seq data
In RNA-seq analysis of murine endometrial samples, sequence reads were aligned to the mouse genome mm39/GRCm39 using HISAT2 version 2.2.1 with the default option [70]. The number of reads at each gene was counted using the featureCounts function in the Rsubread package (v2.10.5) [71]. Differential expression analysis was performed using the TCC R package (https://www.R-project.org/) version 1.30.0 [72]. Genes with a q-value < 0.05 were defined as differentially expressed genes (DEGs). A volcano plot was generated using R with the EnhancedVolcano package (v1.14.0). Gene ontology analysis was performed using ShinyGO 0.77 [73] with DEGs as input.
RNA-seq analysis of the human endometrium was performed as described previously [20]. Raw reads (accession number: GSE207362) were aligned to the human genome sequence GRCh38/hg38 using HISAT2 version 2.1.0, and reads per kilobase of transcript per million mapped reads (RPKM) values were determined using the featureCounts function in the Rsubread package.
Statistical analysis
The two-tailed Mann–Whitney U test was used to compare data between two groups unless otherwise specified. P-values less than 0.05 were considered statistically significant. Data are presented as means ± standard deviation. All experiments were performed at least three times to validate the results. No statistical method was used to predetermine sample size as effect sizes were unknown.
Data availability
The next-generation sequencing data of murine uteri in this study have been deposited in the DNA Data Bank of Japan (DDBJ) Sequence Read Archive under the accession code DRA017380.
References
Wang H, Dey SK. Roadmap to embryo implantation: clues from mouse models. Nat Rev Genet. 2006;7:185–99.
Cha J, Sun X, Dey SK. Mechanisms of implantation: strategies for successful pregnancy. Nat Med. 2012;18:1754–67.
Ma WG, Song H, Das SK, Paria BC, Dey SK. Estrogen is a critical determinant that specifies the duration of the window of uterine receptivity for implantation. Proc Natl Acad Sci USA. 2003;100:2963–8.
Kobayashi R, Terakawa J, Omatsu T, Hengjan Y, Mizutani T, Ohmori Y, et al. The window of implantation is closed by estrogen via insulin-like growth factor 1 pathway. J Reprod Infertil. 2017;18:231–41.
Harton GL, Munne S, Surrey M, Grifo J, Kaplan B, McCulloh DH, et al. Diminished effect of maternal age on implantation after preimplantation genetic diagnosis with array comparative genomic hybridization. Fertil Steril. 2013;100:1695–703.
Ruiz-Alonso M, Blesa D, Diaz-Gimeno P, Gomez E, Fernandez-Sanchez M, Carranza F, et al. The endometrial receptivity array for diagnosis and personalized embryo transfer as a treatment for patients with repeated implantation failure. Fertil Steril. 2013;100:818–24.
Ye X. Uterine luminal epithelium as the transient gateway for embryo implantation. Trends Endocrinol Metab. 2020;31:165–80.
Stewart CL, Kaspar P, Brunet LJ, Bhatt H, Gadi I, Köntgen F, et al. Blastocyst implantation depends on maternal expression of leukaemia inhibitory factor. Nature. 1992;359:76–9.
Kobayashi R, Terakawa J, Kato Y, Azimi S, Inoue N, Ohmori Y, et al. The contribution of leukemia inhibitory factor (LIF) for embryo implantation differs among strains of mice. Immunobiology. 2014;219:512–21.
Sroga JM, Ma X, Das SK. Developmental regulation of decidual cell polyploidy at the site of implantation. Front Biosci. 2012;4:1475–86.
Namiki T, Ito J, Kashiwazaki N. Molecular mechanisms of embryonic implantation in mammals: Lessons from the gene manipulation of mice. Reprod Med Biol. 2018;17:331–42.
Gray CA, Bazer FW, Spencer TE. Effects of neonatal progestin exposure on female reproductive tract structure and function in the adult ewe. Biol Reprod. 2001;64:797–804.
Filant J, Zhou H, Spencer TE. Progesterone inhibits uterine gland development in the neonatal mouse uterus. Biol Reprod. 2012;86:146, 1–9.
Jeong JW, Kwak I, Lee KY, Kim TH, Large MJ, Stewart CL, et al. Foxa2 is essential for mouse endometrial gland development and fertility. Biol Reprod. 2010;83:396–403.
Filant J, DeMayo FJ, Pru JK, Lydon JP, Spencer TE. Fibroblast growth factor receptor two (FGFR2) regulates uterine epithelial integrity and fertility in mice. Biol Reprod. 2014;90:7.
Fang X, Ni N, Lydon JP, Ivanov I, Bayless KJ, Rijnkels M, et al. Enhancer of Zeste 2 polycomb repressive complex 2 subunit is required for uterine epithelial integrity. Am J Pathol. 2019;189:1212–25.
Kim TH, Yoo JY, Choi KC, Shin JH, Leach RE, Fazleabas AT, et al. Loss of HDAC3 results in nonreceptive endometrium and female infertility. Sci Transl Med. 2019;11:eaaf7533.
Nanjappa MK, Mesa AM, Medrano TI, Jefferson WN, DeMayo FJ, Williams CJ, et al. The histone methyltransferase EZH2 is required for normal uterine development and function in mice. Biol Reprod. 2019;101:306–17.
Mesa AM, Mao J, Nanjappa MK, Medrano TI, Tevosian S, Yu F, et al. Mice lacking uterine enhancer of zeste homolog 2 have transcriptomic changes associated with uterine epithelial proliferation. Physiol Genomics. 2020;52:81–95.
Fukui Y, Hirota Y, Aikawa S, Sakashita A, Shimizu-Hirota R, Takeda N, et al. The EZH2-PRC2-H3K27me3 axis governs the endometrial cell cycle and differentiation for blastocyst invasion. Cell Death Dis. 2023;14:320.
Yang SC, Park M, Hong KH, La H, Park C, Wang P, et al. CFP1 governs uterine epigenetic landscapes to intervene in progesterone responses for uterine physiology and suppression of endometriosis. Nat Commun. 2023;14:3220.
Wan S, Sun Y, Zong J, Meng W, Yan J, Chen K, et al. METTL3-dependent m(6)A methylation facilitates uterine receptivity and female fertility via balancing estrogen and progesterone signaling. Cell Death Dis. 2023;14:349.
Zheng ZH, Zhang GL, Jiang RF, Hong YQ, Zhang QY, He JP, et al. METTL3 is essential for normal progesterone signaling during embryo implantation via m(6)A-mediated translation control of progesterone receptor. Proc Natl Acad Sci USA. 2023;120:e2214684120.
Kobayashi R, Kawabata-Iwakawa R, Terakawa J, Sugiyama M, Morita S, Horii T, et al. Aberrant activation of estrogen receptor-α signaling in Mettl14-deficient uteri impairs embryo implantation. FASEB J. 2023;37:e23093.
Heinz S, Romanoski CE, Benner C, Glass CK. The selection and function of cell type-specific enhancers. Nat Rev Mol Cell Biol. 2015;16:144–54.
Schoenfelder S, Fraser P. Long-range enhancer-promoter contacts in gene expression control. Nat Rev Genet. 2019;20:437–55.
Sze CC, Shilatifard A. MLL3/MLL4/COMPASS family on epigenetic regulation of enhancer function and cancer. Cold Spring Harb Perspect Med. 2016;6:a026427.
Hu D, Gao X, Morgan MA, Herz HM, Smith ER, Shilatifard A. The MLL3/MLL4 branches of the COMPASS family function as major histone H3K4 monomethylases at enhancers. Mol Cell Biol. 2013;33:4745–54.
Lee JE, Wang C, Xu S, Cho YW, Wang L, Feng X, et al. H3K4 mono- and di-methyltransferase MLL4 is required for enhancer activation during cell differentiation. Elife. 2013;2:e01503.
Koemans TS, Kleefstra T, Chubak MC, Stone MH, Reijnders MRF, de Munnik S, et al. Functional convergence of histone methyltransferases EHMT1 and KMT2C involved in intellectual disability and autism spectrum disorder. PLoS Genet. 2017;13:e1006864.
Lavery WJ, Barski A, Wiley S, Schorry EK, Lindsley AW. KMT2C/D COMPASS complex-associated diseases [K(CD)COM-ADs]: an emerging class of congenital regulopathies. Clin Epigenetics. 2020;12:10.
Ng SB, Bigham AW, Buckingham KJ, Hannibal MC, McMillin MJ, Gildersleeve HI, et al. Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome. Nat Genet. 2010;42:790–3.
Fagan RJ, Dingwall AK. COMPASS ascending: emerging clues regarding the roles of MLL3/KMT2C and MLL2/KMT2D proteins in cancer. Cancer Lett. 2019;458:56–65.
Rao RC, Dou Y. Hijacked in cancer: the KMT2 (MLL) family of methyltransferases. Nat Rev Cancer. 2015;15:334–46.
Garcia-Sanz P, Trivino JC, Mota A, Perez Lopez M, Colas E, Rojo-Sebastian A, et al. Chromatin remodelling and DNA repair genes are frequently mutated in endometrioid endometrial carcinoma. Int J Cancer. 2017;140:1551–63.
Chakraborty I, Das SK, Wang J, Dey SK. Developmental expression of the cyclo-oxygenase-1 and cyclo-oxygenase-2 genes in the peri-implantation mouse uterus and their differential regulation by the blastocyst and ovarian steroids. J Mol Endocrin. 1996;16:107–22.
Chakrabarty A, Tranguch S, Daikoku T, Jensen K, Furneaux H, Dey SK. MicroRNA regulation of cyclooxygenase-2 during embryo implantation. Proc Natl Acad Sci USA. 2007;104:15144–9.
Song H, Lim H, Das SK, Paria BC, Dey SK. Dysregulation of EGF family of growth factors and COX-2 in the uterus during the preattachment and attachment reactions of the blastocyst with the luminal epithelium correlates with implantation failure in LIF-deficient mice. Mol Endocrinol. 2000;14:1147–61.
Daikoku T, Cha J, Sun X, Tranguch S, Xie H, Fujita T, et al. Conditional deletion of Msx homeobox genes in the uterus inhibits blastocyst implantation by altering uterine receptivity. Dev Cell. 2011;21:1014–25.
Namiki T, Terakawa J, Karakama H, Noguchi M, Murakami H, Hasegawa Y, et al. Uterine epithelial Gp130 orchestrates hormone response and epithelial remodeling for successful embryo attachment in mice. Sci Rep. 2023;13:854.
Tajika Y, Murakami T, Iijima K, Gotoh H, Takahashi-Ikezawa M, Ueno H, et al. A novel imaging method for correlating 2D light microscopic data and 3D volume data based on block-face imaging. Sci Rep. 2017;7:3645.
Kelleher AM, Peng W, Pru JK, Pru CA, DeMayo FJ, Spencer TE. Forkhead box a2 (FOXA2) is essential for uterine function and fertility. Proc Natl Acad Sci USA. 2017;114:E1018–E26.
Chan LN, Wang XF, Tsang LL, Liu CQ, Chan HC. Suppression of CFTR-mediated Cl(-) secretion by enhanced expression of epithelial Na(+) channels in mouse endometrial epithelium. Biochem Biophys Res Commun. 2000;276:40–4.
Ruan YC, Guo JH, Liu X, Zhang R, Tsang LL, Dong JD, et al. Activation of the epithelial Na+ channel triggers prostaglandin E(2) release and production required for embryo implantation. Nat Med. 2012;18:1112–7.
Yang JZ, Ajonuma LC, Tsang LL, Lam SY, Rowlands DK, Ho LS, et al. Differential expression and localization of CFTR and ENaC in mouse endometrium during pre-implantation. Cell Biol Int. 2004;28:433–9.
Froimchuk E, Jang Y, Ge K. Histone H3 lysine 4 methyltransferase KMT2D. Gene. 2017;627:337–42.
Ashokkumar D, Zhang Q, Much C, Bledau AS, Naumann R, Alexopoulou D, et al. MLL4 is required after implantation, whereas MLL3 becomes essential during late gestation. Development. 2020;147:dev186999.
Adam MP, Hudgins L. Kabuki syndrome: a review. Clin Genet. 2005;67:209–19.
Kubo N, Chen PB, Hu R, Ye Z, Sasaki H, Ren B. H3K4me1 facilitates promoter-enhancer interactions and gene activation during embryonic stem cell differentiation. Mol Cell. 2024;84:1742–52.e5.
Hirota Y. Progesterone governs endometrial proliferation-differentiation switching and blastocyst implantation. Endocr J. 2019;66:199–206.
Kelleher AM, DeMayo FJ, Spencer TE. Uterine glands: developmental biology and functional roles in pregnancy. Endocr Rev. 2019;40:1424–45.
Friedman JR, Kaestner KH. The Foxa family of transcription factors in development and metabolism. Cell Mol Life Sci. 2006;63:2317–28.
Zaret KS. Pioneer transcription factors initiating gene network changes. Annu Rev Genet. 2020;54:367–85.
Kim HM, Kang B, Park S, Park H, Kim CJ, Lee H, et al. Forkhead box protein D2 suppresses colorectal cancer by reprogramming enhancer interactions. Nucleic Acids Res. 2023;51:6143–55.
Terakawa J, Rocchi A, Serna VA, Bottinger EP, Graff JM, Kurita T. FGFR2IIIb-MAPK activity is required for epithelial cell fate decision in the lower mullerian duct. Mol Endocrinol. 2016;30:783–95.
Terakawa J, Serna VA, Nair DM, Sato S, Kawakami K, Radovick S, et al. SIX1 cooperates with RUNX1 and SMAD4 in cell fate commitment of Mullerian duct epithelium. Cell Death Differ. 2020;27:3307–20.
Silverberg SG. Problems in the differential diagnosis of endometrial hyperplasia and carcinoma. Mod Pathol. 2000;13:309–27.
Kobayashi R, Kawabata-Iwakawa R, Sugiyama M, Oyama T, Ohtsuka M, Horii T, et al. Multiplexed genome editing by in vivo electroporation of Cas9 ribonucleoproteins effectively induces endometrial carcinoma in mice. Int J Cancer. 2023;152:2331–7.
Franco HL, Dai D, Lee KY, Rubel CA, Roop D, Boerboom D, et al. WNT4 is a key regulator of normal postnatal uterine development and progesterone signaling during embryo implantation and decidualization in the mouse. FASEB J. 2010;25:1176–87.
Lu S, Peng H, Zhang H, Zhang L, Cao Q, Li R, et al. Excessive intrauterine fluid cause aberrant implantation and pregnancy outcome in mice. PLoS ONE. 2013;8:e78446.
Doray A, Lemoine R, Severin M, Chadet S, Lopez-Charcas O, Heraud A, et al. The voltage-gated sodium channel Beta4 subunit maintains epithelial phenotype in mammary cells. Cells. 2021;10:1624.
Johansson JK, Karema-Jokinen VI, Hakanen S, Jylha A, Uusitalo H, Vihinen-Ranta M, et al. Sodium channels enable fast electrical signaling and regulate phagocytosis in the retinal pigment epithelium. BMC Biol. 2019;17:63.
Carrithers LM, Hulseberg P, Sandor M, Carrithers MD. The human macrophage sodium channel NaV1.5 regulates mycobacteria processing through organelle polarization and localized calcium oscillations. FEMS Immunol Med Microbiol. 2011;63:319–27.
Ni N, Jalufka FL, Fang X, McCreedy DA, Li Q. Role of EZH2 in uterine gland development. Int J Mol Sci. 2022;23:15665.
Sirohi VK, Medrano TI, Kannan A, Bagchi IC, Cooke PS. Uterine-specific Ezh2 deletion enhances stromal cell senescence and impairs placentation, resulting in pregnancy loss. iScience. 2023;26:107028.
Horii T, Morita S, Kimura M, Terawaki N, Shibutani M, Hatada I. Efficient generation of conditional knockout mice via sequential introduction of lox sites. Sci Rep. 2017;7:7891.
Berg S, Kutra D, Kroeger T, Straehle CN, Kausler BX, Haubold C, et al. ilastik: interactive machine learning for (bio)image analysis. Nat Methods. 2019;16:1226–32.
Fedorov A, Beichel R, Kalpathy-Cramer J, Finet J, Fillion-Robin JC, Pujol S, et al. 3D Slicer as an image computing platform for the Quantitative Imaging Network. Magn Reson Imaging. 2012;30:1323–41.
Muto J, Fukuda S, Watanabe K, Dai X, Tsuda T, Kiyoi T, et al. Highly concentrated trehalose induces prohealing senescence-like state in fibroblasts via CDKN1A/p21. Commun Biol. 2023;6:13.
Kim D, Langmead B, Salzberg SL. HISAT: a fast spliced aligner with low memory requirements. Nat Methods. 2015;12:357–60.
Liao Y, Smyth GK, Shi W. featureCounts: an efficient general purpose program for assigning sequence reads to genomic features. Bioinformatics. 2014;30:923–30.
Sun J, Nishiyama T, Shimizu K, Kadota K. TCC: an R package for comparing tag count data with robust normalization strategies. BMC Bioinformatics. 2013;14:219.
Ge SX, Jung D, Yao R. ShinyGO: a graphical gene-set enrichment tool for animals and plants. Bioinformatics. 2020;36:2628–9.
Acknowledgements
We appreciate Dr. Jumpei Terakawa in Azabu University, and Dr. Makoto Sugiyama in Kitasato University, for fruitful discussions on this study. We also thank Ms. Kaori Iizuka, Ms. Yuko Okazaki and Ms. Eriko Suetomo for technical supports and maintenance of animals. This work was the result of using research equipment shared with the MEXT Project for promoting public utilization of advanced research infrastructure (Grant Number JPMXS0420600121).
Funding
This work was supported by the Japan Society for the Promotion of Science (JSPS) under Grant Numbers JP19K16021 and JP22K15026 (to RK); the Platform Project for Supporting Drug Discovery and Life Science Research (Basis for Supporting Innovative Drug Discovery and Life Science Research (BINDS)) from the Japan Agency for Medical Research and Development (AMED) under Grant Number JP23ama121049 (to IH); Gunma University for the promotion of scientific research (to IH); and the Takeda Science Foundation (to IH).
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RK and IH designed the research. RK and YT performed the experiments. RK, YT, JK, MS, TH, YM, SA and YH analyzed data. RK, YT, and IH wrote the manuscript. All authors reviewed and edited the paper.
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All animal studies were approved by the Animal Care and Experimentation Committee of Gunma University (approved No. 23-048) and were carried out in accordance with approved guidelines.
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Kobayashi, R., Tajika, Y., Kohmaru, J. et al. The histone methyltransferase KMT2D is essential for embryo implantation via regulating precise differentiation of endometrial cells. Cell Death Discov. 10, 357 (2024). https://doi.org/10.1038/s41420-024-02134-9
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DOI: https://doi.org/10.1038/s41420-024-02134-9
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