Abstract
This review explores the relationship between ovarian aging and senescent cell accumulation, as well as the efficacy of senolytics to improve reproductive longevity. Reproductive longevity is determined by the age-associated decline in ovarian reserve, resulting in reduced fertility and eventually menopause. Cellular senescence is a state of permanent cell cycle arrest and resistance to apoptosis. Senescent cells accumulate in several tissues with advancing age, thereby promoting chronic inflammation and age-related diseases. Ovaries also appear to accumulate senescent cells with age, which might contribute to aging of the reproductive system and whole organism through SASP production. Importantly, senolytic drugs can eliminate senescent cells and may present a potential intervention to mitigate ovarian aging. Herein, we review the current literature related to the efficacy of senolytic drugs for extending the reproductive window in mice.
Similar content being viewed by others
Ovarian reserve and reproductive lifespan
The ovarian reserve is predominantly represented by primordial follicles, a structure composed of an oocyte surrounded by a single layer of pre-granulosa cells, which remains in a quiescent state1. When activated, primordial follicles initiate an irreversible process of development, which can lead to ovulation or atresia2. The activation of primordial follicles is regulated by several growth pathways. Activation of mammalian target of rapamycin (mTOR) in the pre-granulosa cells of the primordial follicle increases the expression of Kit ligand (KITL), which binds to its tyrosine kinase receptor KIT in the oocyte. This activates the phosphoinositide 3-kinase (PI3K)/protein kinase B(AKT) pathway in the oocyte, culminating in the phosphorylation of forkhead box O3a (FOXO3a) in the nucleus and the activation of the primordial follicle3. The progression of ovarian aging is characterized by a gradual reduction, both in quantity and quality, of the oocytes in the ovarian cortex4. Accumulated damage with age in oocytes results in embryonic malformation and an increased rate of miscarriage5. Therefore, ovarian aging is identified as the primary cause of infertility in females6. This decline in the number of primordial follicles is observed with the advancement of age in women4 and in mice7. A reduction in fertility is observed around the age of 35 years in women, followed by menstrual irregularities around 45 years of age4. Infertility is observed in the subsequent years, and eventually, the onset of menopause, characterized by the end of menstrual cycles around 50 years of age4. In C57BL/6 mice, the ovarian reserve is reduced by half by 10 months of age, and by 18 months, it is reduced by approximately 10 times, compared to young adult mice7. Cyclicity is also interrupted between 11 and 16 months of age8, resembling the timeline observed in women. Furthermore, female C57BL/6 mice will cease producing offspring around 18 months of age, with a significant reduction in fertility already observed at 10 months of age7,9. This indicates that even though menopause is not a phenomena observed in mice, there is a severe reduction in ovarian reserve and a decrease in ovulation and fertility, similar to what occurs in women4. This phenomena has been recently referred as oopause, indicating the end of reproductive cyclicity in mammalian species10. This evidence also suggests mice as a valuable model to study reproductive aging.
The cyclical production of female reproductive hormones plays a significant role not only in follicular development but also in women’s overall health11. Antral follicles are the primary source of ovarian estrogen secretion in women of reproductive age12. Due to the reduction in ovarian reserve, the number of antral follicles also reduces with age, decreasing ovarian steroid hormone output, and affecting female health13. As the ovulatory cycles end due to severe depletion of ovarian reserve with age, there is a drastic drop in circulating levels of estradiol, marking the onset of menopause14. Thus, menopause is associated with increased metabolic dysfunction and mortality4,15. During menopause, women experience a variety of symptoms and conditions associated with changes in steroid levels and aging16. This stage of reproductive life significantly increases susceptibility to various metabolic diseases, including cardiovascular diseases17, osteoporosis18, hypertension, diabetes mellitus19 and ovarian cancer16. Women experiencing early menopause (<45 years) further increase these risks, with a substantial impact on public health4,19. In mice, a similar process is observed. Female mice tend to live longer than males, however, when ovaries are surgically removed, life expectancy is reduced20, indicating a clear relationship between reproductive and somatic longevity. Indeed, old female mice receiving ovarian transplants from young mice experience an increase in longevity21.
The reduction of estradiol levels is one of the primary effects of menopause, and several studies highlight the benefits of exogenous estradiol replacement therapy22. However, longevity extension from ovarian tissue transplantation was higher when young ovaries were depleted of follicles with VCD (4-vinylcyclohexene diepoxide) before transplantation23. Additionally, women with more reproductive cycles are at an increased risk of certain pathologies24. In mice, cycling generates a microenvironment that may exacerbate the effect of estrogen-dependent mutagenesis in the endometrium25. Therefore, while preserving the ovarian reserve is beneficial for lifespan extension in most studies in mice and humans, it may contribute to the development of certain pathologies due to increased number of cycles tissues are exposed.
The role of senescent cells in the ovary
The aging process differs from tissue to tissue26,27. The primary feature of aging in most tissues is the accumulation of senescent cells28. Cellular senescence is a state of permanent cell cycle arrest triggered in response to numerous stressors, aiming to inhibit the proliferation of aged and/or damaged cells29. Despite this, senescent cells are metabolically active and secrete inflammatory cytokines, chemokines, growth factors, and matrix metalloproteinases30. These factors are commonly referred to as the senescence-associated secretory phenotype (SASP)31,32. The SASP allows senescent cells to modulate pathways in neighboring and distant cells and tissues33 and has been widely used as a marker of cellular senescence34,35. The SASP recruits immune cells, thereby creating a pro-inflammatory microenvironment in injured or aging tissues29,36. It is important to emphasize that senescence plays physiological roles during normal development and is essential for tissue homeostasis37. However, the chronic accumulation of senescent cells with advancing age results in detrimental effects on health, increasing age-related diseases38,39. Interestingly, the injection of senescent cells into young mice promotes dysfunctions similar to those observed during chronological aging40. This indicates that senescent cells play an active role in the aging process of the organism.
The age-related increase in senescent cells is associated with numerous age-related diseases41 including diabetes mellitus42, atherosclerosis38, Alzheimer’s/Parkinson’s43 and inflammatory diseases44. However, mice experiments revealed that the number of senescent cells can vary between tissues in the same individual45. For the identification of senescent cells, a commonly used strategy is to measure proteins and transcripts of senescence effectors, including p16INK4a (Cdkn2a), p53, and p21 (Cdkn1a)46. Evidence suggests that p53-21 signaling initiates, while p16INK4a signaling is necessary for the maintenance of the senescence state47,48. Additionally, increased senescent cell numbers are associated with the accumulation of senescence-associated β-galactosidase (SA-β-Gal)49 and lipofuscin50. However, senescent cell distribution in tissues is heterogeneous and sometimes hard to determine. In this sense, innovative methodologies, such as spatial transcriptomics, spatial epigenomics, spatial metabolomics can be applied to detect senescent cell activity in each tissue of interest51. Genetic editing of human pluripotent stem cell (hPSCs) was also used to generate senescent cell models52. Others proposed a method called image flow cytometry, which is based on the analysis of cell autofluorescence and morphological parameters with the use of artificial intelligence and machine learning. This method has proven to be simple and fast and can be used regardless of the type of senescent cells53. Although these evidence suggest that senescence markers increase with age in mice, many undergo significant changes only after 12 months of age34,54. As mentioned before, mouse fertility is already compromised at 10 months of age, with a severe reduction in ovarian reserve. Therefore, it is necessary to better understand the role of cellular senescence in the ovary, as this organ shows impairment of its functions much earlier than other tissues.
There is limited data on senescence cell accumulation and their function in the ovary. Although there is no well-defined panel of biomarkers for cellular senescence, some have been widely used in the ovary, including markers of pro-inflammatory stress, double-strand DNA breaks, and lipofuscin55,56,57. Corresponding with reduced ovarian function, there is also a significant increase in markers related to senescence in the ovaries of mice between 3 and 12 months of age (Cdkn1a, Cdkn2a, Pai-1, and Hmgb1), along with the accumulation of lipofuscin aggregates58. Similar accumulation of senescent cells in other organs is observed much later in life, around 18-20 months of age. Additionally, the ovarian transcriptomic profile indicates a positive regulation of genes related to pro-inflammatory stress and cell cycle inhibition, while genes involved in cell cycle progression were negatively regulated, which is characteristic of senescent cells58. Increased SA-β-Gal and p21 levels was detected in the ovarian stroma of mice at 8-10 months of age, indicating senescent cell accumulation59. An increase in the burden of senescent cells, identified through SASP markers, was also observed when cisplatin was used to induce damage in the ovaries of very young mice60. An increase in p16 & p21 expression and lipofuscin aggregates were observed in the ovaries of genetically obese mice compared to lean controls as early as six months of age61. This indicates that markers of senescence in ovarian tissue can be observed before 12 months of age in mice. Similar observations were made in human tissue. Expression of p21 was elevated in ovarian of middle-aged women (>37 years) compared to young controls (<33 years)62. Other senescence and fibrosis related genes were also up-regulated in stromal cells of middle aged compared to younger women62. Expression of these senescence biomarkers are often exacerbated when stressors such as chemotherapy treatment and obesity are present.
As the ovary ages, there is also a well-defined increase in inflammation and changes to extracellular matrix (ECM), including increased collagen deposition63,64. Senescent cells produce a SASP signature, which is often used to identify its tissue accumulation, as discussed earlier. SASP components include soluble factors, such as pro-inflammatory cytokines and proteases involved in tissue remodeling (matrix metalloproteinases [MMPs] and tissue inhibitor of metalloproteinases [TIMP]), but also includes insoluble factors that are ECM components, such as collagen and lamin65. Therefore, it is challenging to separate senescent cells accumulation from the physiological ovarian response of tissue remodeling and accumulation of inflammatory cells observed with age. Pro-inflammatory responses play a significant role in ovarian aging55,66. Most age-related transcriptional changes observed in the ovaries of mice are associated with inflammation and immune responses67. Recent proteomic evaluations appear to mirror these findings68. Age-related increases in cytokines such as interleukin (IL)-6, IL-1β, IL-8, interferon-γ (Infg), TNF-α, and chemokines, such as, monocyte chemoattractant protein-1 (Ccl2), CC motif chemokine ligand (Ccl) 5, and CXC motif chemokine ligand (Cxcl) 2 have been reported in the ovaries of mice55,64,69. Studies in humans have revealed similar findings, with elevated levels of IL-3, IL-6, IL-7, IL-15, Ccl3, and Cxcl10 in the follicular fluid of older women70,71. A recent single-cell transcriptomic and flow cytometry analysis showed age-related accumulation of immune cells in the ovary72. The same report also showed that senescence-associated genes in the ovary are predominantly expressed by immune cells and generally did not change with age. Hence, increased in cellular senescence during ovarian aging may reflect increased immune cell abundance. Interestingly, Cdkn1a expression increased in Type 17T lymphocytes with age, suggesting that this cell population might enter a senescence state in the ovary. Aged ovaries also accumulate multinucleated giant cells (MNGCs), which are believed to result from the fusion of macrophages associated with chronic inflammation55,73. Lipofuscin positivity is considered a senescence marker, however it colocalizes with MNGC, suggesting that either lipofuscin is staining MNGCs, or MNGCs are also in a senescent state72.
Age-related pro-inflammatory stress in the ovary is a conserved phenotype across species and may be causally linked to the decline in oocyte quality, challenges in conception, and the onset of declining fertility4. Dysregulation of immune cells and/or altered inflammatory signaling has been implicated in reproductive declines74. It is known that pro-inflammatory mediators increase the activation of primordial follicles, causing damage in oocyte/embryonic development and decreasing the production of steroid hormones75. Conversely, IL-1 knockout mice have increased ovarian reserve and fertility57. Although the expression of collagen synthesis genes remains constant in the ovary during the reproductive window69,72, there appears to be a decrease in the activity of collagenase72, resulting in the accumulation of collagen and increased tissue stiffness. In turn, this stiffness can hinder ovulation64, and lead to a reduction in fertility in older mice. Nevertheless, macrophages play critical roles in multiple aspects of ovarian functions. Macrophages can be activated and polarized to the M1 or M2 subtype depending on the pro-inflammatory or anti-inflammatory stimulus, respectively76. The increase in M1 macrophages has been associated with increased primordial follicular activation, while the increase in the M2 subtype had inhibitory effects76. The ovulatory process itself is preceded by inflammatory reactions that occur in mature follicles77. Single-cell analysis of ovary, oviduct, uterus, cervix, and vagina indicate these organs undergo recurrent immune infiltration and ECM remodeling in each cycle25. In the uterus, oviduct, and vagina, fibrotic tissue accumulated with aging and continuous cycling. Mice that were induced to estropause had reduced fibrotic tissue in uterus and oviduct, due to reduced number of ovarian cycles25. Ovarian fibrosis seems to be aggravated by persistent chronic inflammation62. This in turn can be due accumulation of pyroptotic macrophages which interact with effector T cells and secrete factors promoting pyropoptosis in a feedback loop62. Therefore, inflammation and tissue remodeling are present in the reproductive tract at all stages of aging, making it difficult to identify the physiological and pathological roles of senescence in this context. However, it also points to modulation of the SASP as an important step in improving fertility.
The use of senolytics to curtail female reproductive aging
Senolytics drugs eliminate senescent cells and have been reported to increase longevity in mice40. Several compounds have been studied for their senolytic properties, including quercetin, dasatinib, fisetin, resveratrol, curcumin, and others78. Quercetin was reported to have senolytic potential in combination with dasatinib79. Quercetin is a flavonoid found in fruits and vegetables that has antioxidant80, anti-inflammatory, and antineoplastic properties81. It inhibits the PI3K signaling pathway and indirectly stimulates the apoptosis of senescent cells82. Dasatinib is a multi-tyrosine kinase inhibitor used in cancer treatment83. Dasatinib targets the ephrin B survival-regulating dependency receptor (Efbn1)82 and anti-apoptotic pathways activated in senescent cells, such as Bcl-2 and Bcl-xL78. Fisetin is also a member of the flavonoid family, found in low concentrations in fruits and vegetables84. It has antineoplastic, neuroprotective, and antioxidant effects84 and has been widely studied for its senolytic effect85. Fisetin also targets the anti-apoptotic pathways Bcl-2 and Bcl-xL86 and inhibits Pi3k/Akt and mTOR pathways87.
The combined use of dasatinib and quercetin (D + Q) selectively targets a broad range of senescent cell types more effectively than when used individually79. D + Q treatment was shown to be safe both in vitro and in vivo, causing the selective elimination of senescent cells and promoting increased lifespan when administered to old mice (19–21 months old)40. Studies have also shown success with the use of the D + Q senolytic cocktail in improving symptoms of age-related diseases in humans with idiopathic pulmonary fibrosis88 and Alzheimer’s disease89. Fisetin also has a senolytic effect, clearing senescent cells and reducing SASP-induced inflammation in vitro and in vivo90. Only one month of fisetin treatment increased the lifespan of progeroid and old wild-type mice (22–24 months of age)85. Some studies also tested the efficacy of senolytics in disease models, such as lupus, atherosclerosis, obesity and Alzheimer61,91,92,93,94,95,96. However, most of these studies were performed with old (19–24 months old) or progeroid mice40,85. Therefore, few studies target healthy females within the reproductive window, typically up to approximately 15 months of age. This implies that senolytics are used when the ovarian reserve is already depleted. As the primordial follicle reserve is not renewed, the damage to fertility is irreversible at this point. Additionally, it is not clear from current studies if the amount of senescent cells accumulated in the ovaries during this reproductive age is sufficient to have any impact in fertility when cleared by senolytic treatments.
In this regard, a reduction in the levels of p21, p16, and lipofuscin was observed in the ovaries of genetically obese mice treated with D + Q at six months of age61. However, we observed that D + Q treatment in healthy females from one six months of age did not affect ovarian reserve or fertility97. Additionally, treatment of females with D + Q or fisetin from six to 12 months of age also did not affect ovarian reserve and fertility97. Fisetin reduced macrophage infiltration and lipofuscin staining in ovarian tissue97. Some SASP markers were reduced while others were increased by senolytic treatment97. This indicates a small effect of senolytics in ovarian senescence markers, which did not translate into preserved ovarian reserve or improved fertility. Granulosa cells treated with quercetin alone had attenuated cell injury and aging induced by H2O2, activating protective autophagy and up-regulating autophagy-related proteins98. This suggests that quercetin alone could improve ovarian function. Treatment of young female and male mice (4–13 months old) with D + Q and fisetin has controversial effects. While fisetin improved glucose and energy metabolism, reduced SASP, and enhanced cognitive performance in young male mice, D + Q had minimal effects99. Conversely, D + Q was detrimental in females, increasing SASP expression and fat accumulation, reducing energy metabolism, and cognitive performance, while fisetin had no significant effects99. These findings indicate that age and sex are key determinants of the effectiveness of senolytics. Taken together, these data suggest that the use of senolytics in young female mice of reproductive age does not benefit ovarian reserve and fertility and may even have detrimental effects.
In this context, it is known that chemotherapy agents contribute to infertility, early menopause, and premature ovarian failure in young women undergoing cancer treatment100. Chemoterapy agents cause an hyperactivation of primordial follicles through massive apoptosis of growing follicles and reduced AMH levels101. Young female mice (6 weeks old) received cisplatin one week after starting a four-week course of D + Q treatment. Cisplatin reduced the ovarian reserve and induced ovarian senescence, as demonstrated by in vitro staining of granulosa cells with SA-β-Gal and in vivo immunohistochemistry for SA-β-Gal, p16, p21, and IL-660. Treatment with D + Q reduced the senescent cell burden and preserved the ovarian reserve, reducing DNA damage and ovarian fibrosis, resulting in increased litter sizes60. Similarly, mice treated with the chemotherapeutic agent doxorubicin had increased ovarian senescent cell burden. The accumulation of senescent cells in the ovaries after doxorubicin treatment was determined through increased SA-β-Gal, p16 and p21102. Once again, D + Q and fisetin reduced senescent cell burden in treated mice. However, senolytics did not reverse the follicular loss and ovarian stromal fibrosis caused by doxorubicin102. In this experiment, the dose of doxorubicin was administered on the day following the first administration of senolytics D + Q, and the treatment lasted for three weeks. Conversely, when mice received the chemotherapeutic one week after starting treatment with senolytics, positive effects in the ovarian reserve were observed60. This suggests that senolytics may be acting to prevent damage caused by chemotherapeutical agents rather than being able to reverse any damage caused by established senescent cells and subsequent depletion of the ovarian reserve.
Nicotinamide adenine dinucleotide (NAD) also emerges as a promising regulator in attenuating age-related functional decline and associated diseases. NAD metabolism can influence SASP production by senescent cells103. As ovarian aging progresses, there is a reduction in NAD levels, which presents promising strategies for intervention104,105. Disruption of the NAD pathway results in decreased ovarian NAD levels, mitochondrial dysfunction, diminished ovarian reserve, and reduced oocyte quality in old mice106. This highlights the potential of NAD precursors supplementation to preserve oocyte quality and ovarian health. CD38, one of the enzymes that consumes NAD107, is predominantly expressed in the ovarian extrafollicular space, especially in immune cells, and its levels increase with age108. The absence of CD38 results in increased ovarian NAD levels and fertility in young mice, associated to a greater initial ovarian reserve108. Given the link between NAD levels and SASP production, more studies focused on ovarian senescent cells are needed to understand its role in fertility.
Future directions
There are few studies using senolytics in young reproductive age mice available in the literature, which suggest that the compounds currently used have few beneficial systemic benefits at this age window. Even fewer studies evaluated the effects of senolytics in the ovary. These suggest that senolytics may prevent ovarian reserve loss, but cannot reverse the damage to the ovarian reserve after senescence is established. The activation of primordial follicles is an irreversible process, which means that the damage promoted by senescent cells in the ovarian reserve would not be able to be reverted by senolytics. This may indicate the direction for future studies, focusing on preventing accumulation of senescent cells in the ovaries in order to prevent declines in fertility. Additionally, the inflammation generated by senescent cells through the SASP itself can contribute to irreversible follicular activation. Therefore, it is possible that other senolytic compounds with greater efficacy in the ovary need to be tested. Compounds with senomorphic activity, i.e. able to decrease SASP secretion, may be considered to prevent the negative pro-inflammatory environment generated by senescent cells in the ovary. Furthermore, the physiological role of senescent cells in reproductive functions must be considered, as inflammation and tissue remodeling are key points in the ovulatory process in females. Therefore, the path to validating the use of senotherapies in female reproductive aging is still open. A better understanding of ovarian senescence biomarkers and the role of senescent cells on female fertility is still necessary in order to define how to promote targeted elimination of these cells without negative impact on other organs in young females.
References
Park, S. U., Walsh, L. & Berkowitz, K. M. Mechanisms of ovarian aging. Reproduction 162, R19–R33 (2021).
te Velde, E. R., Scheffer, G. J., Dorland, M., Broekmans, F. J. & Fauser, B. C. Developmental and endocrine aspects of normal ovarian aging. Mol. Cell Endocrinol. 145, 67–73 (1998).
Zhang, H. et al. Somatic cells initiate primordial follicle activation and govern the development of dormant oocytes in mice. Curr. Biol. 24, 2501–2508 (2014).
Broekmans, F. J., Soules, M. R. & Fauser, B. C. Ovarian aging: mechanisms and clinical consequences. Endocr. Rev. 30, 465–493 (2009).
Vollenhoven, B. & Hunt, S. Ovarian ageing and the impact on female fertility. F1000Res. 7, https://doi.org/10.12688/f1000research.16509.1 (2018)
Tesarik, J., Galan-Lazaro, M. & Mendoza-Tesarik, R. Ovarian Aging: Molecular Mechanisms and Medical Management. Int. J. Mol. Sci. 22, https://doi.org/10.3390/ijms22031371 (2021).
Kevenaar, M. E. et al. Serum anti-mullerian hormone levels reflect the size of the primordial follicle pool in mice. Endocrinology 147, 3228–3234 (2006).
Felicio, L. S., Nelson, J. F. & Finch, C. E. Longitudinal studies of estrous cyclicity in aging C57BL/6J mice: II. Cessation of cyclicity and the duration of persistent vaginal cornification. Biol. Reprod. 31, 446–453 (1984).
Selesniemi, K., Lee, H. J. & Tilly, J. L. Moderate caloric restriction initiated in rodents during adulthood sustains function of the female reproductive axis into advanced chronological age. Aging Cell 7, 622–629 (2008).
Winkler, I. & Goncalves, A. Do mammals have menopause? Cell 186, 4729–4733 (2023).
Atwood, C. S. & Bowen, R. L. The reproductive-cell cycle theory of aging: an update. Exp. Gerontol. 46, 100–107 (2011).
Camaioni, A. et al. The process of ovarian aging: it is not just about oocytes and granulosa cells. J. Assist Reprod. Genet 39, 783–792 (2022).
Colella, M. et al. Ovarian Aging: Role of Pituitary-Ovarian Axis Hormones and ncRNAs in Regulating Ovarian Mitochondrial Activity. Front. Endocrinol. 12, 791071 (2021).
Hall, J. E. Endocrinology of the Menopause. Endocrinol. Metab. Clin. North Am. 44, 485–496 (2015).
Xu, X., Jones, M. & Mishra, G. D. Age at natural menopause and development of chronic conditions and multimorbidity: results from an Australian prospective cohort. Hum. Reprod. 35, 203–211 (2020).
Dunneram, Y., Greenwood, D. C. & Cade, J. E. Diet, menopause and the risk of ovarian, endometrial and breast cancer. Proc. Nutr. Soc. 78, 438–448 (2019).
El Khoudary, S. R. et al. Menopause Transition and Cardiovascular Disease Risk: Implications for Timing of Early Prevention: A Scientific Statement From the American Heart Association. Circulation 142, e506–e532 (2020).
Prestwood, K. M. & Raisz, L. G. Prevention and treatment of osteoporosis. Clin. Cornerstone 4, 31–41 (2002).
Nappi, R. E., Chedraui, P., Lambrinoudaki, I. & Simoncini, T. Menopause: a cardiometabolic transition. Lancet Diab. Endocrinol. 10, 442–456 (2022).
Benedusi, V. et al. Ovariectomy shortens the life span of female mice. Oncotarget 6, 10801–10811 (2015).
Mason, J. B., Cargill, S. L., Anderson, G. B. & Carey, J. R. Transplantation of young ovaries to old mice increased life span in transplant recipients. J. Gerontol. A Biol. Sci. Med. Sci. 64, 1207–1211 (2009).
Salpeter, S. R. et al. Meta-analysis: effect of hormone-replacement therapy on components of the metabolic syndrome in postmenopausal women. Diab. Obes. Metab. 8, 538–554 (2006).
Habermehl, T. L. et al. Extension of longevity and reduction of inflammation is ovarian-dependent, but germ cell-independent in post-reproductive female mice. Geroscience 41, 25-38 (2019).
Gavrilyuk, O., Braaten, T., Weiderpass, E., Licaj, I. & Lund, E. Lifetime number of years of menstruation as a risk index for postmenopausal endometrial cancer in the Norwegian Women and Cancer Study. Acta Obstet. Gynecol. Scand. 97, 1168–1177 (2018).
Winkler, I. et al. The cycling and aging mouse female reproductive tract at single-cell resolution. Cell 187, 981–998.e925 (2024).
Schaum, N. et al. Ageing hallmarks exhibit organ-specific temporal signatures. Nature 583, 596–602 (2020).
Tabula Muris, C. A single-cell transcriptomic atlas characterizes ageing tissues in the mouse. Nature 583, 590–595 (2020).
Lopez-Otin, C., Blasco, M. A., Partridge, L., Serrano, M. & Kroemer, G. The hallmarks of aging. Cell 153, 1194–1217 (2013).
Di Micco, R., Krizhanovsky, V., Baker, D. & d’Adda di Fagagna, F. Cellular senescence in ageing: from mechanisms to therapeutic opportunities. Nat. Rev. Mol. Cell Biol. 22, 75–95 (2021).
Kumari, R. & Jat, P. Mechanisms of Cellular Senescence: Cell Cycle Arrest and Senescence Associated Secretory Phenotype. Front. Cell Dev. Biol. 9, 645593 (2021).
Secomandi, L., Borghesan, M., Velarde, M. & Demaria, M. The role of cellular senescence in female reproductive aging and the potential for senotherapeutic interventions. Hum. Reprod. Update 28, 172–189 (2022).
Cuollo, L., Antonangeli, F., Santoni, A. & Soriani, A. The Senescence-Associated Secretory Phenotype (SASP) in the Challenging Future of Cancer Therapy and Age-Related Diseases. Biology 9, https://doi.org/10.3390/biology9120485 (2020).
Ovadya, Y. & Krizhanovsky, V. Senescent cells: SASPected drivers of age-related pathologies. Biogerontology 15, 627–642 (2014).
Hudgins, A. D. et al. Age- and Tissue-Specific Expression of Senescence Biomarkers in Mice. Front. Genet 9, 59 (2018).
Wang, Z., Liu, H. & Xu, C. Cellular Senescence in the Treatment of Ovarian Cancer. Int J. Gynecol. Cancer 28, 895–902 (2018).
Fane, M. & Weeraratna, A. T. How the ageing microenvironment influences tumour progression. Nat. Rev. Cancer 20, 89–106 (2020).
McHugh, D. & Gil, J. Senescence and aging: Causes, consequences, and therapeutic avenues. J. Cell Biol. 217, 65–77 (2018).
Minamino, T. et al. Endothelial cell senescence in human atherosclerosis: role of telomere in endothelial dysfunction. Circulation 105, 1541–1544 (2002).
Wang, J. et al. Vascular Smooth Muscle Cell Senescence Promotes Atherosclerosis and Features of Plaque Vulnerability. Circulation 132, 1909–1919 (2015).
Xu, M. et al. Senolytics improve physical function and increase lifespan in old age. Nat. Med. 24, 1246–1256 (2018).
Mylonas, A. & O’Loghlen, A. Cellular Senescence and Ageing: Mechanisms and Interventions. Front. Aging 3, 866718 (2022).
Minamino, T. et al. A crucial role for adipose tissue p53 in the regulation of insulin resistance. Nat. Med. 15, 1082–1087 (2009).
Chinta, S. J. et al. Cellular senescence and the aging brain. Exp. Gerontol. 68, 3–7 (2015).
Ashiqueali, S. A. et al. Fisetin modulates the gut microbiota alongside biomarkers of senescence and inflammation in a DSS-induced murine model of colitis. Geroscience, https://doi.org/10.1007/s11357-024-01060-z (2024)
Baker, D. J. et al. Naturally occurring p16(Ink4a)-positive cells shorten healthy lifespan. Nature 530, 184–189 (2016).
Schafer, M. J., Miller, J. D. & LeBrasseur, N. K. Cellular senescence: Implications for metabolic disease. Mol. Cell Endocrinol. 455, 93–102 (2017).
Alcorta, D. A. et al. Involvement of the cyclin-dependent kinase inhibitor p16 (INK4a) in replicative senescence of normal human fibroblasts. Proc. Natl Acad. Sci. USA 93, 13742–13747 (1996).
Beausejour, C. M. et al. Reversal of human cellular senescence: roles of the p53 and p16 pathways. EMBO J. 22, 4212–4222 (2003).
Valieva, Y., Ivanova, E., Fayzullin, A., Kurkov, A. & Igrunkova, A. Senescence-Associated beta-Galactosidase Detection in Pathology. Diagnostics 12, https://doi.org/10.3390/diagnostics12102309 (2022)
Evangelou, K. & Gorgoulis, V. G. Sudan Black B, The Specific Histochemical Stain for Lipofuscin: A Novel Method to Detect Senescent Cells. Methods Mol. Biol. 1534, 111–119 (2017).
Chen, P., Wang, Y. & Zhou, B. Insights into targeting cellular senescence with senolytic therapy: The journey from preclinical trials to clinical practice. Mech. Ageing Dev. 218, 111918 (2024).
Goh, K. J., Chen, J. H., Rocha, N. & Semple, R. K. Human pluripotent stem cell-based models suggest preadipocyte senescence as a possible cause of metabolic complications of Werner and Bloom Syndromes. Sci. Rep. 10, 7490 (2020).
Malavolta, M. et al. Simple Detection of Unstained Live Senescent Cells with Imaging Flow Cytometry. Cells 11, https://doi.org/10.3390/cells11162506 (2022).
Yousefzadeh, M. J. et al. Tissue specificity of senescent cell accumulation during physiologic and accelerated aging of mice. Aging Cell 19, e13094 (2020).
Briley, S. M. et al. Reproductive age-associated fibrosis in the stroma of the mammalian ovary. Reproduction 152, 245–260 (2016).
Saccon, T. D. et al. Primordial follicle reserve, DNA damage and macrophage infiltration in the ovaries of the long-living Ames dwarf mice. Exp. Gerontol. 132, 110851 (2020).
Uri-Belapolsky, S. et al. Interleukin-1 deficiency prolongs ovarian lifespan in mice. Proc. Natl Acad. Sci. USA 111, 12492–12497 (2014).
Ansere, V. A. et al. Cellular hallmarks of aging emerge in the ovary prior to primordial follicle depletion. Mech. Ageing Dev. 194, 111425 (2021).
Maruyama, N. et al. Accumulation of senescent cells in the stroma of aged mouse ovary. J. Reprod. Dev. 69, 328–336 (2023).
Du, D. et al. Senotherapy Protects against Cisplatin-Induced Ovarian Injury by Removing Senescent Cells and Alleviating DNA Damage. Oxid. Med. Cell Longev. 2022, 9144644 (2022).
Hense, J. D. et al. Senolytic treatment reverses obesity-mediated senescent cell accumulation in the ovary. Geroscience 44, 1747–1759 (2022).
Zhou, C. et al. Single-Cell Atlas of Human Ovaries Reveals The Role Of The Pyroptotic Macrophage in Ovarian Aging. Adv. Sci., e2305175. https://doi.org/10.1002/advs.202305175 (2023).
Amargant, F. et al. Ovarian stiffness increases with age in the mammalian ovary and depends on collagen and hyaluronan matrices. Aging Cell 19, e13259 (2020).
Umehara, T. et al. Female reproductive life span is extended by targeted removal of fibrotic collagen from the mouse ovary. Sci. Adv. 8, eabn4564 (2022).
Coppe, J. P., Desprez, P. Y., Krtolica, A. & Campisi, J. The senescence-associated secretory phenotype: the dark side of tumor suppression. Annu. Rev. Pathol. 5, 99–118 (2010).
Zhang, Z., Schlamp, F., Huang, L., Clark, H. & Brayboy, L. Inflammaging is associated with shifted macrophage ontogeny and polarization in the aging mouse ovary. Reproduction 159, 325–337 (2020).
Schneider, A. et al. Ovarian transcriptome associated with reproductive senescence in the long-living Ames dwarf mice. Mol. Cell Endocrinol. 439, 328–336 (2017).
Dipali, S. S. et al. Proteomic quantification of native and ECM-enriched mouse ovaries reveals an age-dependent fibro-inflammatory signature. Aging 15, 10821–10855 (2023).
Lliberos, C. et al. Evaluation of inflammation and follicle depletion during ovarian ageing in mice. Sci. Rep. 11, 278 (2021).
Babayev, E. & Duncan, F. E. Age-associated changes in cumulus cells and follicular fluid: the local oocyte microenvironment as a determinant of gamete quality. Biol. Reprod. 106, 351–365 (2022).
Hashemitabar, M. et al. A proteomic analysis of human follicular fluid: comparison between younger and older women with normal FSH levels. Int J. Mol. Sci. 15, 17518–17540 (2014).
Isola, J. V. V. et al. A single-cell atlas of the aging mouse ovary. Nat Aging, https://doi.org/10.1038/s43587-023-00552-5 (2024).
Foley, K. G., Pritchard, M. T. & Duncan, F. E. Macrophage-derived multinucleated giant cells: hallmarks of the aging ovary. Reproduction 161, V5–V9 (2021).
Nteeba, J., Ortinau, L. C., Perfield, J. W. 2nd & Keating, A. F. Diet-induced obesity alters immune cell infiltration and expression of inflammatory cytokine genes in mouse ovarian and peri-ovarian adipose depot tissues. Mol. Reprod. Dev. 80, 948–958 (2013).
Bromfield, J. J. & Sheldon, I. M. Lipopolysaccharide reduces the primordial follicle pool in the bovine ovarian cortex ex vivo and in the murine ovary in vivo. Biol. Reprod. 88, 98 (2013).
Xiao, Y. et al. Macrophage-derived extracellular vesicles regulate follicular activation and improve ovarian function in old mice by modulating local environment. Clin. Transl. Med. 12, e1071 (2022).
Espey, L. L. Ovulation as an inflammatory reaction—a hypothesis. Biol. Reprod. 22, 73–106 (1980).
Martel, J. et al. Emerging use of senolytics and senomorphics against aging and chronic diseases. Med. Res. Rev. https://doi.org/10.1002/med.21702 (2020).
Zhu, Y. et al. The Achilles’ heel of senescent cells: from transcriptome to senolytic drugs. Aging Cell 14, 644–658 (2015).
Wang, K. et al. Fisetin induces apoptosis through mitochondrial apoptosis pathway in human uveal melanoma cells. Environ. Toxicol. 33, 527–534 (2018).
Hwang, H. V., Tran, D. T., Rebuffatti, M. N., Li, C. S. & Knowlton, A. A. Investigation of quercetin and hyperoside as senolytics in adult human endothelial cells. PLoS One 13, e0190374 (2018).
Soto-Gamez, A. & Demaria, M. Therapeutic interventions for aging: the case of cellular senescence. Drug Discov. Today 22, 786–795 (2017).
Montero, J. C., Seoane, S., Ocana, A. & Pandiella, A. Inhibition of SRC family kinases and receptor tyrosine kinases by dasatinib: possible combinations in solid tumors. Clin. Cancer Res. 17, 5546–5552 (2011).
Khan, N., Syed, D. N., Ahmad, N. & Mukhtar, H. Fisetin: a dietary antioxidant for health promotion. Antioxid. Redox Signal 19, 151–162 (2013).
Yousefzadeh, M. J. et al. Fisetin is a senotherapeutic that extends health and lifespan. EBioMedicine 36, 18–28 (2018).
Zhu, Y. et al. New agents that target senescent cells: the flavone, fisetin, and the BCL-X(L) inhibitors, A1331852 and A1155463. Aging 9, 955–963 (2017).
Chamcheu, J. C. et al. Fisetin, a 3,7,3’,4’-Tetrahydroxyflavone Inhibits the PI3K/Akt/mTOR and MAPK Pathways and Ameliorates Psoriasis Pathology in 2D and 3D Organotypic Human Inflammatory Skin Models. Cells 8, 1089 (2019).
Justice, J. N. et al. Senolytics in idiopathic pulmonary fibrosis: Results from a first-in-human, open-label, pilot study. EBioMedicine, https://doi.org/10.1016/j.ebiom.2018.12.052 (2019).
Gonzales, M. M. et al. Senolytic Therapy to Modulate the Progression of Alzheimer’s Disease (SToMP-AD): A Pilot Clinical Trial. J. Prev. Alzheimers Dis. 9, 22–29 (2022).
Hambright, W. S. et al. The Senolytic Drug Fisetin Attenuates Bone Degeneration in the Zmpste24 (-/-) Progeria Mouse Model. J. Osteoporos. 2023, 5572754 (2023).
Schafer, M. J. et al. Cellular senescence mediates fibrotic pulmonary disease. Nat. Commun. 8, 14532 (2017).
Musi, N. et al. Tau protein aggregation is associated with cellular senescence in the brain. Aging Cell 17, e12840 (2018).
Zhang, P. et al. Senolytic therapy alleviates Abeta-associated oligodendrocyte progenitor cell senescence and cognitive deficits in an Alzheimer’s disease model. Nat. Neurosci. 22, 719–728 (2019).
Palmer, A. K. et al. Targeting senescent cells alleviates obesity-induced metabolic dysfunction. Aging Cell 18, e12950 (2019).
Roos, C. M. et al. Chronic senolytic treatment alleviates established vasomotor dysfunction in aged or atherosclerotic mice. Aging Cell 15, 973–977 (2016).
Ijima, S. et al. Fisetin reduces the senescent tubular epithelial cell burden and also inhibits proliferative fibroblasts in murine lupus nephritis. Front. Immunol. 13, 960601 (2022).
Garcia, D. N. et al. Senolytic treatment fails to improve ovarian reserve or fertility in female mice. Geroscience, https://doi.org/10.1007/s11357-024-01089-0 (2024).
Cai, M. et al. Quercetin activates autophagy to protect rats ovarian granulosa cells from H(2)O(2)-induced aging and injury. Eur. J. Pharm. 966, 176339 (2024).
Fang, Y. et al. Sexual dimorphic metabolic and cognitive responses of C57BL/6 mice to Fisetin or Dasatinib and quercetin cocktail oral treatment. Geroscience 45, 2835–2850 (2023).
Cui, W. et al. Preventing ovarian failure associated with chemotherapy. Med. J. Aust. 209, 412–416 (2018).
Kalich-Philosoph, L. et al. Cyclophosphamide triggers follicle activation and “burnout”; AS101 prevents follicle loss and preserves fertility. Sci. Transl. Med. 5, 185ra162 (2013).
Gao, Y. et al. Increased cellular senescence in doxorubicin-induced murine ovarian injury: effect of senolytics. Geroscience 45, 1775–1790 (2023).
Nacarelli, T. et al. NAD(+) metabolism governs the proinflammatory senescence-associated secretome. Nat. Cell Biol. 21, 397–407 (2019).
Bertoldo, M. J. et al. NAD(+) Repletion Rescues Female Fertility during Reproductive Aging. Cell Rep. 30, 1670–1681.e1677 (2020).
Yang, Q. et al. Increasing ovarian NAD(+) levels improve mitochondrial functions and reverse ovarian aging. Free Radic. Biol. Med. 156, 1–10 (2020).
Yang, Q. et al. Deletion of enzymes for de novo NAD(+) biosynthesis accelerated ovarian aging. Aging Cell 22, e13904 (2023).
Aksoy, P., White, T. A., Thompson, M. & Chini, E. N. Regulation of intracellular levels of NAD: a novel role for CD38. Biochem. Biophys. Res. Commun. 345, 1386–1392 (2006).
Perrone, R. et al. CD38 regulates ovarian function and fecundity via NAD(+) metabolism. iScience 26, 107949 (2023).
Acknowledgements
This work was supported by CAPES and CNPq. This project has been made possible in part by grant number 1023 from the Global Consortium for Reproductive Longevity & Equality (GCRLE).
Author information
Authors and Affiliations
Contributions
JDH, JVVI, MBS and AS conceptualized and designed this review. JDH, JVVI, DNG, LSM and MMM contribute to writing specific sections. All authors reviewed and approved the final submitted manuscript.
Corresponding author
Ethics declarations
Competing interests
The authors declare no competing interests.
Additional information
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Hense, J.D., Isola, J.V.V., Garcia, D.N. et al. The role of cellular senescence in ovarian aging. npj Aging 10, 35 (2024). https://doi.org/10.1038/s41514-024-00157-1
Received:
Accepted:
Published:
DOI: https://doi.org/10.1038/s41514-024-00157-1
- Springer Nature Limited