Intratracheal administration of adipose derived mesenchymal stem cells alleviates chronic asthma in a mouse model
Adipose-derived mesenchymal stem cell (ASCs) exerts immunomodulatory roles in asthma. However, the underlying mechanism remains unclear. The present study aimed to explore the effects and mechanisms of ASCs on chronic asthma using an ovalbumin (OVA)-sensitized asthmatic mouse model.
Murine ASCs (mASCs) were isolated from male Balb/c mice and identified by the expression of surface markers using flow cytometry. The OVA-sensitized asthmatic mouse model was established and then animals were treated with the mASCs through intratracheal delivery. The therapy effects were assessed by measuring airway responsiveness, performing immuohistochemical analysis, and examining bronchoalveolar lavage fluid (BALF). Additionally, the expression of inflammatory cytokines and lgE was detected by CHIP and ELISA, respectively. The mRNA levels of serum indices were detected using qRT-PCR.
The mASCs grew by adherence with fibroblast-like morphology, and showed the positive expression of CD90, CD44, and CD29 as well as the negative expression of CD45 and CD34, indicating that the mASCs were successfully isolated. Administering mASCs to asthmatic model animals through intratracheal delivery reduced airway responsiveness, the number of lymphocytes (P < 0.01) and the expression of lgE (P < 0.01), IL-1β (P < 0.05), IL-4 (P < 0.001), and IL-17F (P < 0.001), as well as increased the serum levels of IL-10 and Foxp3, and the percentage of CD4 + CD25 + Foxp3+ Tregs in the spleen, and reduced the expression of IL-17 (P < 0.05) and RORγ.
Intratracheal administration of mASCs alleviated airway inflammation, improved airway remodeling, and relieved airway hyperresponsiveness in an OVA-sensitized asthma model, which might be associated with the restoration of Th1/Th2 cell balance by mASCs.
KeywordsChronic asthma Airway hyperresponsiveness Mesenchymal stem cells Regulatory T cells
Adipose-derived mesenchymal stem cell
Bronchoalveolar lavage fluid
Least significant difference
Mesenchymal stem cells
Phosphate buffer saline
Th1 lymphocytes/Th2 lymphocytes
As a common chronic respiratory disease, the prevalence of asthma keeps increases every year . The characteristics of asthma include bronchial hyperreactivity and symptoms of airway obstruction . The combination of corticosteroids and long-acting β2-adrenoceptor agonists is widely used to control asthma in most patients . However, asthma is not yet cured and clinical symptoms are still difficult to alleviate . Therefore, it is necessary to explore novel therapies and their mechanisms.
Multiple types of cells are involved in asthma pathology, including eosinophils, mast cells, T lymphocytes, invariant NKT cells, basophils, type 2 innate lymphoid cells (ILC2s) and others . An imbalance of Th1 lymphocytes/Th2 lymphocytes (Th1/Th2) is thought to be involved in asthma pathogenesis of asthma , but this imbalance cannot fully explain the pathological mechanism of asthma. Regulatory T cells (Tregs), including natural regulatory T cells (nTregs) and inducible/adaptive regulatory T cells (iTregs or Tregs), play a more critical role in autoimmune diseases and allergic diseases through regulating helper T cells . The phenotype of Tregs is characterized by constitutively high expression of cell surface molecules, such as CD25/GITR/CTLA4 and the transcription factor Foxp3 . The role of Tregs in asthma has been demonstrated in both human and animal studies [7, 8, 9]. Shi et al. found that the Th2 response is associated with a deficiency of CD4 + CD25 + Tregs in patients with asthma . Tao et al. revealed that Tregs are significantly less abundant in children with allergic rhinitis (AR) accompanyied by bronchial asthma (BA) than those with AR or BA alone or control subjects . In a mouse asthma model of asthma, infusing CD4+ CD25+ Tregs can alleviate airway inflammation and airway hyperresponsiveness through increasing the serum level of IL-10 .
Mesenchymal stem cells (MSCs), pluripotent cells derived from early mesoderm, can differentiate into fat, bone, cartilage, epithelial cells and endothelial cells . Many studies have reported that MSCs are beneficial to the remission of asthma remission [12, 13, 14]. It has been demonstrated that when MSCs are infused into mice with ovalbumin (OVA)-sensitized asthma, the serum IgE level is significantly downregulated and airway inflammation is markedly relieved [15, 16]. Importantly, adipose-derived mesenchymal stem cells (ASCs) reduce inflammation and induce Tregs in immune disorders such as rheumatoid arthritis . However, the effects and mechanisms of ASCs in asthma have rarely been reported.
In the present study, mouse ASCs (mASCs) were intratracheally applied into mice in an OVA-sensitized chronic asthma model, and then the clinical symptoms of mouse asthma were extensively investigated. The underlying mechanisms were also revealed.
The Ethics Committee of Shanghai Jiaotong University (Shanghai, China) approved this study. Ten male and eighty female Balb/c mice of 6–8 weeks age and 16–18 g weight were provided by Shanghai Silaike Laboratory Animal Co., Ltd. (Shanghai, China) and fed in the animal experimental center of school of Medicine, Shanghai Jiao Tong University at suitable environment. The male mice were fed with high fat diet for 4 weeks while the female mice were provided normal food and water under a 12 h/12 h light/dark cycle.
Isolation and culture of murine ASCs
The male Balb/c mice were sacrificed via cervical dislocation and immersed into 75% alcohol for 2 min. Then, the groin subcutaneous fat tissues were aseptically removed and minced with scissors, followed by washing with phosphate buffer saline (PBS) and digestion with collagenase I . The mASCs were obtained after the floating fat and undigested tissues were centrifuged. Next, the mASCs were resuspended in serum-free medium, inoculated into a T75 flask and cultured in a 37°C incubator with 5% CO2.
The expression of CD90, CD44, CD29, CD34 and CD45 on mASCs was detected using flow cytometry (FACS, Epics Altra, Coulter, Beckman, USA). When the confluency of mASCs reached 80–90%, the cell density was adjusted to 1 × 106/ml. Then the cell suspensions were acquired from mASCs of the mice, respectively. The FACS was conducted after incubation with antibodies against CD90-PE, CD44-PE, CD29-PE, CD34-PE, and CD45-PE (BD Pharmingen, San Diego, USA).
Animal model, grouping and administration
Female Balb/c mice were randomly divided into four groups containing ten mice each group: PBS + PBS group, PBS + mASCs group, OVA + PBS group, and OVA+ mASCs group. An OVA-sensitized allergic asthma model was established following a previously described procedure . Briefly, the mice in the PBS + PBS and PBS + mASCs groups were intraperitoneally injected with 100 μl PBS while the mice in the OVA + PBS and OVA + mASCs groups were intraperitoneally injected with 100 μl of 0.1% OVA (Sigma-Aldrich, Saint Louis, Missouri, USA) at Days 0, 7, and 14. Then, the mice were anesthetized by injecting 30 μl chloral hydrate and fixed in the operation panel. The mouse headswere lift, keeping an angle of 30° between the head and the ground. Mouse tongues were pulled out with wide-nose pliers, and the trace syringe was inserted into the trachea directly by the laryngeal glottis under laryngoscopy. In total, 30 μl of PBS were intratracheally injected into the mice of the PBS + PBS and OVA + PBS groups at Day 21 via endotracheal instillation. At the same time, 1 × 106 mASCs in 30 μl PBS were intratracheally injected into the mice of the PBS + mASCs and OVA + mASCs groups. Thirty minutes after the transplantation, the mice were maintained in a chamber filled with 2.5% atomized-OVA for an extra 30 min. All the mice were challenged for 30 min with 2.5% atomized-OVA 3 times a week for 8 consecutive weeks. All female Balb/c mice were sacrificed within 24 h after the last atomized-OVA challenge through intraperitoneal injection of 300 mg/kg pentobarbital sodium.
Airway hyperresponsiveness test
The mice were anesthetized by injecting 5 mg/kg midazolam and 100 mg/kg alcidione. Then airway responsiveness was determined with an EMMS system (EMMS, Hampshire, UK) by measuring lung resistance (RL) in response to inhaled methacholine (MCh; Sigma-Aldrich) at concentrations of 4 to 256 mg/mL for 20 s. The provocative challenge 100 (PC100) was calculated from the dose of MCh at which RL was 100% above the baseline level.
Preparation of bronchoalveolar lavage fluid
BALF was obtained by lavaging the trachea with cold PBS three times . After centrifugation, the supernatants were used for cytokine analysis. The cell pellets were resuspended in PBS. The total number of cells was calculated under a microscope after Trypan blue staining, and the number of neutrophils, eosinophils, macrophages, and lymphocytes was determined after staining with Wright and Giemsa solutions.
The left lung was fixed with 10% formalin solution for 24 h and embedded in paraffin. Then the samples were prepared using a standard protocol. The 5-μm-thick sections were subjected to HE, MASSON and AB-PAS staining according to previously described methods . Besides, the expression of Muc5AC was visualized by immunohistochemical analysis after adding an anti-Muc5AC antibody (Abcam, Cambridge, UK).
The percentage of CD4 + CD25 + Foxp3+ Tregs in spleen
The cells were filtrated after the spleen was fully ground and red blood cells were removed with erythrocyte lysis buffer. After washing twice with PBS, spleen cells were stained with anti-mouse CD4-FITC, CD25-APC, and Foxp3-PE antibodies (eBioscience, San Diego, CA, USA). The percentage of CD4 + CD25 + Foxp3+ Tregs was analyzed by flow cytometry (Epics Altra, Coulter, Beckman, USA).
Quantitative real-time PCR (qRT-PCR) analysis
Total RNA of right lung tissues was extracted using Trizol (Invitrogen, Carlsbad, California, USA) and cDNA samples were prepared by a first strand cDNA synthesis kit (Promega, Wisconsin, Madison, USA) thereafter. The sequences of the primers were as follows: Foxp3, forward-5′-GCCTTCAGACGAGACTTG-3′, reverse − 5′-CATTGGGTTCTTGTCAGAG-3′; RORγt, forward-5′-CAGGAG CATGGAAGT-CGTC-3′, reverse-5′-CCGTGTAGAGGGCAATCTCA-3′; IL-10, forward-5′-CCCTT-TGCTATGGTGTCCT-3′, reverse-5′-GGATCTCCCTGGTTTCTCTT-3′; IL-17F, forward-5′-AGGGAAGAAGCAGCCATT-3′, reverse-5′-CCAACATCAACAGTAG-CAAA-3′; and β-actin, forward-5′-CAGAAGGACTCCTACGTG-3′, reverse-5′-GCTCGGTCAGGATCTTCATG-3′. β-actin was measured as an internal control. The relative expression of mRNA was normalized to expression of β-actin.
Measurement of inflammatory cytokines in serum and BALF
Serum samples were obtained from mice in the four groups. Firstly, the mice were fixed in a supine position and the hair of the anterior chest was cut. After the skin was disinfected, 800 μl of blood was extracted from the area with the strongest heart beat using the cardiac puncture method. Then, the blood samples were centrifuged and the serum samples were obtained. Protein was extracted from the serum and BALF samples. In total, 50 μl of protein samples were acquired and normalized to the standard samples gradient elution on a slide. Fluorescein was measured as a detection signal. The expression of IL-1β, IL-4, IL-10 and IL-17F was quantified using CHIP by comparing the signal of these genes with those of the standard samples, respectively. Additionally, protein expression of IgE was measured by ELISA kits (eBioscience, San Diego, CA, USA) according to the manufacturer’s instructions.
Data were analyzed by SPSS21.0 software and presented as mean ± standard deviation. A normality test and homogeneity variance analysis were first conducted to analyze the data. Then, the differences among multiple groups were determined using one-way ANOVA followed by the Fishers least significant difference (LSD) method. P < 0.05 was considered to be statistically significant.
The morphological observation of mASCs and the expression of their surface markers
Effect of mASCs on the pathomorphology of lung tissue in OVA-induced asthma model mice
Effect of mASCs on lung function and airway hyperresponsiveness in OVA-induced asthma model mice
Effect of mASCs on the percentage of CD4 + CD25 + Foxp3 + Tregs in spleen in OVA-induced asthma model mice
Effect of mASCs on cell count and subsets in BALF in OVA-induced asthma model mice
Effect of mASCs on inflammatory cytokines in OVA-induced asthma model mice
Asthma is an airway chronic inflammatory disease of the airway involving a variety of cells and components. This chronic inflammation is associated with airway hyperresponsiveness. The mouse asthma model used in the present study perfectly mimicked the pathophysiological characteristics of human asthma. The results demonstrated that intratracheal administration of mASCs could not only reduce airway hyperresponsiveness, inflammatory cell infiltration, and Muc5ac secretion, but also improve airway remodeling.
Th1/Th2 cell imbalance is involved in asthma pathogenesis . Th1 cells exert a protective effect on asthma through releasing IFN-γ and IL-2, while Th2 cells mainly secrete IL-4, IL-5, and IL-13, and then promote the development of asthma [23, 24]. IL-4 can promote the secretion of IgE and increase the secretion of Muc5ac protein in the airway, which leads to high airway response [23, 24]. In this study, we found that Th1 cell secretion was insufficient while Th2 cell secretion was excessive in a chronic asthma mouse model. Furthermore, the expression of serum IL-1β, IL-4 and IL-17F was higher in the asthmatic model compared to those being transplanted by mASCs, indicating that cell therapy might improve the degree of asthma airway inflammation and airway remodeling through regulating the Th1/Th2 ratio. Our results were similar with those of a study by Nemeth .
The malfunction of Tregs is another important mechanism of asthma. Growing evidences shows that asthma is closely related to Tregs . The decline in the number of Tregs as well as their function in asthma is an important manifestation of an immune disorders . A previous study showed that human and mouse MSCs could be induced into CD4 + CD25+ Tregs both in vitro and in vivo, and the immune regulation mediated by MSCs was associated with an increase in number of T cells and the associated cytokine levels . In the present study, the ratio of Tregs to CD4+ T lymphocytes in spleen of asthma model animals was significantly lower than that of the normal group, while the administration of mASCs improved the percentage of Tregs, and reduced the degree of infiltration of inflammatory cells in small bronchial and vascular submucosal tissues in chronic asthmatic mice. Importantly, the transplantation of mASCs showed no influence on normal lung tissue.
As pro-inflammatory cells, Th17 cells can induce the occurrence of asthma and autoimmune diseases by secreting inflammatory factors such as IL-17A, IL-17F, IL-6 and tumor necrosis factor-α . RORγt is the key transcription factor regulating Th17 cell differentiation . In the present study, the IL-17F level in serum and BALF was higher in asthmatic model than that in normal mice, while the IL-10 level was lower in asthmatic model animals. Applying mASCs could downregulate IL-17 and RORγ in asthmatic mice, and upregulate IL-10 and FOXP3, implying that cell therapy could restore the balance of Th17/Treg cells through suppressing the differentiation of Th17 cells and inducing the transcription of Foxp3, which ultimately alleviated airway inflammation and remodeling.
In conclusion, intratracheal administration of mASCs could alleviate the airway inflammation of lung tissue in an OVA-sensitized mouse asthma model, improve airway remodeling and relieve airway hyperresponsiveness. The mechanism might be associated with the restoration of Th1/Th2 cell balance by mASCs.
This work was supported by National Nature Science Foundation of China (Program No. 81470216) and Shanghai Municipal Planning Commission of science and Research Fund.
This work was supported by National Nature Science Foundation of China (Program No. 81470216) and Shanghai Municipal Planning Commission of science and Research Fund.
Availability of data and materials
All data generated or analysed during this study are included in this published article.
Conception and design of the research: RD and GS. Acquisition of data: GY. Analysis and interpretation of data: RD and XH. Statistical analysis: RD and YN. Obtaining funding: GS and RD. Drafting the manuscript: YY. Revision of manuscript for important intellectual content: GS and RD. All authors read and approved the final manuscript.
Ethics approval and consent to participate
This study was approved by Ethics Committee of Shanghai Jiaotong University, School of Medicine.
Consent for publication
The authors declare that they have no competing interests.
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