- Open Access
Therapeutic effects of human umbilical cord mesenchymal stem cell-derived microvesicles on premature ovarian insufficiency in mice
Stem Cell Research & Therapy volume 10, Article number: 250 (2019)
Premature ovarian insufficiency (POI) is one of the leading causes of female infertility, which is caused by an abnormal ovarian reserve. Currently, there is no effective treatment to restore the fertility of POI patients. Recent studies suggested that microvesicles (MVs) released from mesenchymal stem cells (MSCs) exert therapeutic effects in various degenerative diseases. In this study, the effect of human umbilical cord MSC-derived MVs (HUCMSC-MVs) on the restoration of ovarian function in a chemotherapy-induced POI mouse model is investigated.
MVs were obtained from the supernatant of cultured HUCMSCs. The localization of PKH26-labeled HUCMSC-MVs in ovarian tissues was observed by confocal laser scanning microscopy. Histomorphometric analysis was performed to count the number of ovarian follicles and vessels. The ovarian sections were stained with anti-CD34 to evaluate angiogenesis. The levels of estradiol (E2) and follicle-stimulating hormone (FSH) were measured by enzyme-linked immunosorbent serologic assay. The mRNA expression of angiogenesis-related cytokines and the protein expression of AKT in mouse ovaries were measured by quantitative RT-PCR and western blot analysis. The parametric variables were compared by Student’s t test and analysis of variance. The non-parametric variables were compared by the Mann-Whitney U test. Categorical variables were compared by χ2 test. P < 0.05 was considered statistically significant.
PKH26-labeled HUCMSC-MVs were detectable within the ovaries and migrated to the ovarian follicles 24 h after transplantation. The transplantation of HUCMSC-MVs could increase the body weight and number of ovarian follicles (primordial, developing, and preovulatory follicles), induce ovarian angiogenesis, and recover the disturbed estrous cycle of POI mice. The expression levels of total AKT, p-AKT, and angiogenic cytokines (including VEGF, IGF, and angiogenin) in the ovaries of POI mice were markedly upregulated after HUCMSC-MVs transplantation, suggesting that HUCMSC-MVs transplantation might recover ovarian function by inducing angiogenesis via the PI3K/AKT signaling pathway.
This study provides valuable insight into the effects of HUCMSC-MVs on ovarian tissue angiogenesis and on the restoration of ovarian function in POI mice, which may be helpful to develop a treatment strategy for POI patients.
Premature ovarian insufficiency (POI) is a common cause of infertility and is characterized by hypoestrogenism and increased levels of gonadotropins, resulting from the exhaustion of the ovarian follicles. It affects 1–2% of women younger than 40 years of age and 0.1% of women younger than 30. Women with POI usually suffer from primary or secondary amenorrhea, infertility, hot flushes, sexual dysfunction, and/or vaginal dryness, leading to poor quality of life. Moreover, POI is a heterogeneous disorder of multi-factorial origin that is clinically irreversible, and currently, no proven effective therapy exists. Therefore, new and effective treatment strategies are urgently required [1,2,3,4].
Stem cells, which possess the characteristics of rapid self-renewal, indefinite proliferative capacity, multi-directional differentiation potential, and the capacity to produce paracrine factors, have been demonstrated to play an important role in rescuing injured tissues . Stem cells have been successfully used in the restoration of ovarian function in a cyclophosphamide (CTX)-induced POI mouse model [6,7,8,9,10]. However, their cellular and molecular mechanisms have not been fully elucidated. Moreover, a growing amount of evidence indicates that stem cell therapy may have certain adverse effects, including a high risk of cancer and autoimmune disease [11,12,13].
Microvesicles (MVs), small vesicles with a diameter of < 1 μm carrying membrane and cytoplasmic constituents of cellular origin, can transfer proteins, mRNA, and bioactive lipids to target cells through surface-expressed ligands and surface receptors, which affect the phenotype and function of the target cells [14, 15]. It has been reported that MVs released from mesenchymal stem cells (MSCs) exert a protective effect on tissues and stimulate tissue repair in vitro and in vivo, and MV transplantation is a novel cell-free therapeutic strategy for various degenerative disorders [16,17,18]. In this study, we aimed to investigate (i) the effects of human umbilical cord MSC-derived MVs (HUCMSC-MVs) on the functional recovery of injured ovaries in a POI mouse model and (ii) the underlying mechanisms.
Materials and methods
Specific pathogen-free (SPF) grade CD1 (ICR) female mice between 4 and 5 weeks of age were housed under a 12-h light-dark cycle at 25 °C ± 2 °C with food and water provided ad libitum, and all animal experiment protocols were approved by the Ethics Committee of Anhui Medical University.
Isolation and identification of HUCMSC-MVs
HUCMSCs were obtained from Cell Therapy Center of 105th Hospital of the People’s Liberation Army (PLA) and cultured in α-MEM (Gibco, USA) containing 10% fetal bovine serum (FBS, Sijiqing, China) at 37 °C and 5% CO2. When reaching 70–80% confluence, the culture medium was replaced with α-MEM deprived of FBS, then the cells were cultured for 48 h. MVs were obtained from the supernatant of cultured HUCMSCs according to the protocol . The amount of MVs was determined by measuring the total MV-associated proteins, using the Bradford assay. The MVs dissolved in PBS were loaded on copper grids and stained with 1% (w/v) phosphotungstic acid (PTA) and then observed under a transmission electron microscope (FEI, USA). The protein expressions of CD9, CD63, TSG101, and CANX in the HUCMSC-MVs obtained in this study were compared with UC-MSCs by western blot.
Establishment of mice premature ovarian insufficiency model
Four- to 5-week-old female ICR mice (n = 8) with a normal estrous cycle were used to establish POI model, and the other 8 were served as normal control. To build the POI model, busulfan (20 mg/kg, Sigma-Aldrich, USA) and CTX (200 mg/kg, Sigma-Aldrich, USA) dissolved in dimethyl sulfoxide (DMSO) (Sigma-Aldrich, USA) were administered through single intraperitoneal injection, while the subjects in normal control were injected with DMSO only instead of CTX/BUS. Vaginal smears were obtained at 9:00 am daily and stained with hematoxylin and eosin (HE) for analysis of the estrous cycle. The POI mouse model was evaluated 2 weeks later.
Detection of transplanted HUCMSC-MVs in the ovaries
Another 20 mice were enrolled to analyze the localization of the HUCMSC-MVs in the ovary, with 10 for POI model and 10 for normal control, respectively. To detect the HUCMSC-MVs in the ovary, 150 μg PKH26-labeled (Sigma-Aldrich, USA) HUCMSC-MVs were injected into the mice of POI model and normal control via the vena caudalis. The ovaries of 2 mice from each group were taken at 12 h, 24 h, 48 h, 72 h, and 1 week; the frozen sections of the ovarian tissue were stained with human follicle-stimulating hormone receptor (FSHR) (Abcam, USA) for cytoplasm, while the nuclei were stained with diamidino-phenyl-indole (DAPI, Beyotime, China). The localization of PKH26-labeled HUCMSC-MVs in ovarian tissues was observed by confocal laser scanning microscopy.
Intervention of POI model with HUCMSC-MVs
After the POI model was successfully built, other 24 experimental mice were recruited for the evaluation of the therapeutic efficacy of HUCMSC-MVs on POI mice. They were assigned into normal control group, POI group, and POI-MVs group, with 8 mice for each group, and received different interventions. Briefly, the mice were put in the special container (50 ml test tube with several free breath holes), and their tails leaked out. The tail was disinfected with 75% alcohol, then 100 μl of PBS containing 150 μg MVs was injected into the vena caudalis of the mice with 1 ml syringe for the POI-MVs group, while an equivalent of PBS was sham injected into the vena caudalis of the mice in the control group and POI group. The operation was repeated once a week. Four weeks later, assessment of ovarian function and histomorphometric analysis were carried out for each group (Fig. 5a).
Histomorphometric analysis of the ovarian follicles and vessels
The ovaries from the normal control group, POI group, and POI-MVs group were fixed with 4% paraformaldehyde (4 °C, overnight), dehydrated through a grade ethanol series, vitrified in xylene, embedded in paraffin, serially sectioned at 5 μm, and then stained with hematoxylin and eosin (HE). The sections were examined and photographed with the Olympus BX-51 light microscope (Olympus, Japan) . The number of follicles including non-atretic, atretic primordial, developing, and preovulatory follicles in each ovary was counted in every randomly selected tenth section. Only the follicles containing a round oocyte with a clearly visible nucleus were scored as healthy, while the ones convoluted, condensed, or fragmented were scored as atretic [21, 22]. Blood vessel counting was carried out at 200-fold field, and five random fields from three different sections were chosen for each sample.
For the observation of angiogenesis in the ovary, the ovarian section was immunostained with CD34 antibody, a marker for newly formed vascular endothelial cells. Briefly, the ovarian tissue section was incubated with rabbit anti-mice CD34 antibody (Abcam, USA, diluted1:150) overnight at 4 °C, followed by goat anti-rabbit IgG secondary antibody (Abcam, USA, 1:200) for 60 min, then stained with DAB Substrate Kit (Beyotime, China). Hematoxylin was used to co-stain the nuclei. The number of CD34-positive cells was determined by counting five random fields of three different sections from each sample.
Blood sample was collected via the orbital artery of mice after anesthetized with inhaled isofurane (#B506, Abbott, Chicago, IL) and centrifuged at 1600 rpm for 10 min. The serum was stored at − 20 °C until measurement. The levels of estradiol (E2) and follicle-stimulating hormone (FSH) were measured with ELISA Kit (Cusabio, China).
Real-time PCR and western blot
Total RNA of mice ovarian tissue was isolated with Trizol Reagent (Invitrogen, USA). cDNA was synthesized using PrimeScript®RT Master Mix (Takara Bio, Japan) according to the manufacturer’s instructions. qPCR was performed in ABI 7500 real-time PCR system (Applied Biosystems, USA) using SYBR®Premix Ex Taq™ II Kit (Takara Bio, Japan). Primers of vascular endothelial growth factor (VEGF), type 1 insulin-like growth factor (IGF-1), and Angiogenin were designed to span the introns by Roche Universal ProbeLibrary (Table 1), and the specificity and efficiency were confirmed by melting curve and agarose electrophoresis before RT-qPCR. Relative quantification of the gene expression was calculated using the 2-ΔΔCt method normalized to β-actin.
Protein of mice ovarian tissue was separated in 12% SDS-PAGE gels and transferred to PVDF membranes blocked with 5% non-fat milk solution then probed with antibodies against VEGF (1:2000, ThermoFisher, USA), total AKT (1:2000, CST, USA), p-Akt (1:2000, CST, USA), and β-actin (1:3000, Kangcheng, China). The bands were visualized on X-ray films using ECL reagents (Thermo Fisher, USA).
The data are presented as the means ± SEM. The parametric variables were compared by Student’s t test and analysis of variance. The non-parametric variables were compared by the Mann-Whitney U test. Categorical variables were compared by the χ2 test. P < 0.05 was considered statistically significant.
Characterization of HUCMSC-MVs
By electron microscopy, HUCMSC-MVs were characterized as round-shaped membrane vesicles of approximately 30–200 nm in diameter (Fig. 1a, b). The total protein content of MVs released in 48 h by 106 HUCMSCs under serum-free condition was 162.66 ± 17.50 μg. Western blot showed that the HUCMSC-MVs obtained in this study were highly positive for CD9, CD63, and TSG101 and negative for CANX (Fig. 1c), suggesting they originated from MSCs.
Evaluation of the established POI model
The body weight of POI mice was significantly lower than that in the control group. POI mice had an irregular estrous cycle; they exhibited a shorter proestrus and estrus and a longer diestrus [Fig. 2A (e–h)]. The total number of follicles, including atretic, healthy, primordial, developing, and preovulatory follicles, was significantly lower (P < 0.05), while the proportion of the atretic follicles in the POI group was significantly higher than that in the control group (P < 0.05; Fig. 2B). In addition, degeneration of oocytes, severe interstitial fibrosis in ovarian tissue, hypoestrogenism, and increased levels of FSH were observed in POI mice [Fig. 2A (k, l) and C]. Collectively, these results suggest ovarian dysfunction in POI mice.
Location of HUCMSC-MVs in the ovary
PKH26-labeled MVs were detectable in ovarian tissue of both POI mice and normal mice 12 h after administration; the fluorescence intensity in the ovarian tissue was markedly enhanced, and PKH26 was taken up into the cytoplasm of granulosa cells (GCs) 24 h later. The signals remained strong for at least 72 h and disappeared 7 days later (Fig. 3).
HUCMSC-MVs transplantation improved body weight and estrous cycle of POI mice
The mice were weighed once a week after CTX/BUS administration. The body weight of POI-MVs mice was increased significantly after 2 weeks (P < 0.05), although it was still lower than that in the control group after 6 weeks (P < 0.05; Fig. 4a). The estrous cycle of POI-MVs mice recovered gradually 2 weeks after HUCMSC-MVs transplantation, and 75% of POI-MVs mice showed a regular estrous cycle, including a normal diestrus, proestrus, estrus, and metestrus, 4 and 6 weeks after HUCMSC-MVs transplantation. The estrous cycle of POI mice remained irregular throughout the entire experiment (Fig. 4b).
HUCMSC-MVs transplantation increased the ovarian follicles of POI mice
The numbers of primordial, developing, and preovulatory follicles in POI-MVs mice were higher than those in the POI group (P < 0.05). Furthermore, the proportion of atretic follicles was lower, and more healthy follicles were observed in the POI-MVs group (P < 0.05). However, the numbers of total, healthy, primordial, developing, and preovulatory follicles in the POI-MVs group were still lower than those in the control group 4 weeks after MVs transplantation (P < 0.05; Fig. 5b, c).
HUCMSC-MVs transplantation improved hormone secretion in POI mice
Four weeks after MVs transplantation, the serum level of E2 was significantly higher and that of FSH was significantly lower in the POI-MVs group compared with the POI group (P < 0.05), but neither of the two reached the levels of the control group (Fig. 6).
HUCMSC-MVs transplantation induced angiogenesis and cytokine expression in the ovaries of POI mice
HE staining showed that there were more cords, tubules, and blood-filled channels containing red blood cells in the ovaries of POI-MVs mice, and the number of blood vessels in the ovaries of POI-MVs mice had increased significantly 4 weeks after HUCMSC-MVs transplantation (P < 0.05; Fig. 7a, c). By IHC analysis, we detected that the number of CD34-positive cells in the ovaries of POI mice was significantly lower compared with the control mice (P < 0.05). Conversely, more CD34-positive cells were observed in the POI-MVs group (P < 0.05; Fig. 7b, d). The RT-PCR results also showed that the mRNA expression levels of angiogenesis-related cytokines, including VEGF, IGF-1, and angiogenin, in the ovaries of POI mice were downregulated significantly, whereas all of those in the POI-MVs group were upregulated significantly compared with the POI group (P < 0.05; Fig. 8).
HUCMSC-MVs transplantation activated the PI3K/AKT signaling pathway in the ovary
The phosphatidylinositol-3-kinase (PI3K)/AKT signaling pathway participates in various cellular biological processes, including angiogenesis, and phosphorylation of AKT is known to be an index of PI3K/AKT signaling pathway activation. The western blot results demonstrated that the expression of total AKT, p-AKT, and VEGF in the ovaries of the POI-MVs group was significantly higher compared with the POI group (P < 0.05; Fig. 9).
At present, there is no effective therapy or medication for the treatment of POI. Hormone replacement therapy (HRT), one of the most commonly used treatments for POI, only aims to ameliorate the symptoms caused by the disturbed hormone profile and fails to solve the fundamental problem and restore ovarian function and fertility. Moreover, HRT notably increases the risk of thrombosis and cancer [23, 24]. In recent years, therapeutic effects of stem cells derived from a number of sources, including bone marrow, amniotic fluid, and adipose tissue, on long-term infertility and ovarian damage have been reported [25,26,27]. However, the disadvantages resulting from stem cell therapy, including ambiguous curative effects, high risk of cancer, and autoimmune diseases, cannot be ignored [11,12,13].
MVs and extracellular membrane vesicles that can transfer proteins, lipids, and mRNAs from the parent cell to target cells play a key role in intercellular and even interorgan communication . Various cell types can release MVs when they are activated. Among those, MSCs, which exhibit a secretory activity that is at least 10 times higher than that of other cells, are believed to be the main MVs-producing cells . It has been shown that MVs secreted by MSCs can reduce tissue injury through modulating immune responses and promoting self-repair of injured cells , and the components of MSC-derived conditioned medium, such as soluble factors, MVs, and potential organelles, possess many therapeutic properties, indicating that MSC engraftment might not be required . Therefore, MVs transplantation, a new cell-free therapy, may provide a novel strategy to treat POI in practice.
GCs are essential components of the ovarian follicles, playing a supportive and regulatory role in the maturation and development of oocytes and aiding in the maintenance of the hormonal balance in the ovarian niche via the autocrine and paracrine mechanisms. To validate that HUCMSC-MVs could target and be internalized into GCs, PKH26-labeled HUCMSC-MVs were injected into the vena caudalis of model mice, and frozen sections of FSHR-positive ovarian tissue (specific for GCs) were observed under a confocal laser scanning microscope. Red fluorescent signals of PKH26-labeled HUCMSC-MVs were detected in GCs 24 h after transplantation, and the signals remained strong for at least 72 h, indicating that HUCMSC-MVs could target and be internalized into both POI and control mouse ovarian tissue. As the signals almost disappeared 7 days later, the administration of MVs via the vena caudalis in the POI-MVs group was repeated once a week for a month.
Our results show that the disturbed estrous cycle, the levels of E2 and FSH, and the body weight of POI mice exhibited a significant recovery after HUCMSC-MVs transplantation, consistent with a previous study . Moreover, the numbers of primordial, developing, and preovulatory follicles in the ovaries of the POI-MVs group were significantly higher, and the numbers of healthy and atretic follicles were similar to those in the control group 4 weeks after HUCMSC-MVs transplantation. Collectively, these results indicate that HUCMSC-MVs transplantation could prevent follicle atresia and restore the ovarian function of CTX/BUS-induced POI mice.
Ovarian function and follicle development strongly depend on the establishment and continuous remodeling of a complex vascular system in the ovary, which enables the follicle and/or corpus luteum to receive the required supply of nutrients, oxygen, and hormonal support and to synthesize and release steroids [33, 34, 35]. Besides, the formation of a rich vascular network in the primary follicles is considered to be responsible for the selection of the dominant follicle. It has been reported that transplantation of human adipose-derived MSCs could restore damaged ovarian function through inducing angiogenesis and improving the number of ovarian follicles and corpora lutea . In this study, we first illustrated that the number of blood vessels and CD34-positive cells in the ovaries of POI-MVs mice was significantly higher 4 weeks after HUCMSC-MVs transplantation, indicating that MVs transplantation could induce angiogenesis and promote the formation of new blood vessels in the chemotherapy-injured ovary.
Angiogenic factors play important roles in various aspects of neovascularization, including cell proliferation, differentiation, migration, and morphogenesis of vascular cells, and MVs derived from HUCMSCs contain many angiogenesis promoting biomolecules, such as angiogenin, VEGF, VEGF-R2, and MCP-1; some of these are present at higher levels in MVs than in parent cells . VEGF, IGF-1, and angiogenin are well-known angiogenic factors participating in the regulation of follicular development through vascular-independent mechanisms [37,38,39,40]. Our results show the mRNA expression levels of VEGF, IGF-1, and angiogenin in the ovaries of POI-MVs mice are significantly higher than those in POI mice, suggesting that high expression of angiogenic factors induced by HUCMSC-MVs might play a critical role in the restoration of ovarian function.
As is well known, the PI3K-AKT pathway, a key signaling pathway implicated in angiogenesis, regulates the expression of downstream angiogenic factors such as VEGF [41, 42]. Hung et al. found that MSC-conditioned medium under hypoxic conditions could inhibit apoptosis of endothelial cells and stimulate angiogenesis via activation of the PI3K-AKT pathway . Moreover, Jia et al. confirmed that bone marrow mesenchymal stromal cell transplantation could ameliorate angiogenesis and reduce renal damage in rats by activating the PI3K-AKT signaling pathway and increasing serum VEGF level . In this study, we demonstrated that the expression levels of total AKT, p-AKT, and VEGF in the ovary of POI-MVs mice were significantly higher than those in POI mice, indicating that HUCMSC-MVs transplantation might activate the PI3K-AKT signaling pathway and promote VEGF expression. The mechanism by which MVs activate the AKT signaling pathway will be the subject of future research.
There are some limitations in this study. Firstly, a natural mating trial would provide supplementary evidence to prove the effect of MVs in restoring damaged ovarian function; these experiments have been carried out and are described in another publication. Secondly, the biggest challenge for MVs therapy may be the exploration of molecular mechanisms involved in the angiogenesis-promoting effects, which will be the subject of our future work.
Considering the human clinical application of MVs, several concerns remain to be addressed. Firstly, there are two ways of transplanting MVs, that is, the local injection of MVs into the ovarian tissue or into the blood circulation. We have not compared the efficiency of these two methods in our study. Secondly, as is well known, angiogenesis plays a critical role in tumor growth, and it is uncertain whether high doses of MVs can cause serious adverse effects, such as ovarian cancer. Therefore, more work on the efficiency and safety of the in vivo use of MVs must be done before it can be applied in clinical practice.
We first demonstrated that HUCMSC-derived MVs transplantation could restore ovarian function of POI mice model via activation of the PI3K-AKT signaling pathway and promoting angiogenesis of the damaged ovary, which may provide a potential therapeusis for the patients with POI.
Availability of data and materials
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
Hormone replacement therapy
Human umbilical cord mesenchymal stem cell-derived microvesicles
Type 1 insulin-like growth factor
Mesenchymal stem cells
Premature ovarian insufficiency
Vascular endothelial growth factor
Collins G, Patel B, Thakore S, Liu J. Primary ovarian insufficiency: current concepts. South Med J. 2017;110(3):147–53.
De Vos M, Devroey P, Fauser BC. Primary ovarian insufficiency. Lancet. 2010;376(9744):911–21.
Shelling AN. Premature ovarian failure. Reproduction. 2010;140(5):633–41.
Tucker EJ, Grover SR, Bachelot A, Touraine P, Sinclair AH. Premature ovarian insufficiency: new perspectives on genetic cause and phenotypic spectrum. Endocr Rev. 2016;37(6):609–35.
Staal FJ, Baum C, Cowan C, Dzierzak E, Hacein-Bey-Abina S, Karlsson S, Lapidot T, Lemischka I, Mendez-Ferrer S, Mikkers H, et al. Stem cell self-renewal: lessons from bone marrow, gut and iPS toward clinical applications. Leukemia. 2011;25(7):1095–102.
Lee HJ, Selesniemi K, Niikura Y, Niikura T, Klein R, Dombkowski DM, Tilly JL. Bone marrow transplantation generates immature oocytes and rescues long-term fertility in a preclinical mouse model of chemotherapy-induced premature ovarian failure. J Clin Oncol. 2007;25(22):3198–204.
Camussi G, Deregibus MC, Tetta C. Paracrine/endocrine mechanism of stem cells on kidney repair: role of microvesicle-mediated transfer of genetic information. Curr Opin Nephrol Hypertens. 2010;19(1):7–12.
Takehara Y, Yabuuchi A, Ezoe K, Kuroda T, Yamadera R, Sano C, Murata N, Aida T, Nakama K, Aono F, et al. The restorative effects of adipose-derived mesenchymal stem cells on damaged ovarian function. Lab Investig. 2013;93(2):181–93.
Xiao GY, Cheng CC, Chiang YS, Cheng WT, Liu IH, Wu SC. Exosomal miR-10a derived from amniotic fluid stem cells preserves ovarian follicles after chemotherapy. Sci Rep. 2016;6:23120.
Xiao GY, Liu IH, Cheng CC, Chang CC, Lee YH, Cheng WT, Wu SC. Amniotic fluid stem cells prevent follicle atresia and rescue fertility of mice with premature ovarian failure induced by chemotherapy. PLoS One. 2014;9(9):e106538.
Zhu W, Huang L, Li Y, Qian H, Shan X, Yan Y, Mao F, Wu X, Xu WR. Mesenchymal stem cell-secreted soluble signaling molecules potentiate tumor growth. Cell Cycle. 2011;10(18):3198–207.
Sekkate S, Kairouani M, Serji B, M’Rabti H, El Ghissassi I, Errihani H. Granulosa cell tumors of the ovary. Bull Cancer. 2014;101(1):93–101.
Monsel A, Zhu YG, Gudapati V, Lim H, Lee JW. Mesenchymal stem cell derived secretome and extracellular vesicles for acute lung injury and other inflammatory lung diseases. Expert Opin Biol Ther. 2016;16(7):859–71.
Gyorgy B, Szabo TG, Pasztoi M, Pal Z, Misjak P, Aradi B, Laszlo V, Pallinger E, Pap E, Kittel A, et al. Membrane vesicles, current state-of-the-art: emerging role of extracellular vesicles. Cell Mol Life Sci. 2011;68(16):2667–88.
Bidarimath M, Khalaj K, Kridli RT, Kan FW, Koti M, Tayade C. Extracellular vesicle mediated intercellular communication at the porcine maternal-fetal interface: a new paradigm for conceptus-endometrial cross-talk. Sci Rep. 2017;7:40476.
Lee C, Mitsialis SA, Aslam M, Vitali SH, Vergadi E, Konstantinou G, Sdrimas K, Fernandez-Gonzalez A, Kourembanas S. Exosomes mediate the cytoprotective action of mesenchymal stromal cells on hypoxia-induced pulmonary hypertension. Circulation. 2012;126(22):2601–11.
Bian S, Zhang L, Duan L, Wang X, Min Y, Yu H. Extracellular vesicles derived from human bone marrow mesenchymal stem cells promote angiogenesis in a rat myocardial infarction model. J Mol Med (Berl). 2014;92(4):387–97.
Huang-Doran I, Zhang CY, Vidal-Puig A. Extracellular vesicles: novel mediators of cell communication in metabolic disease. Trends Endocrinol Metab. 2017;28(1):3–18.
Théry C, Amigorena S, Raposo G, Clayton A. Isolation and characterization of exosomes from cell culture supernatants and biological fluids. Curr Protocols Cell Biol. 2006;3:22 21–23.22.29.
Cha SK, Shin DH, Kim BY, Yoon SY, Yoon TK, Lee WS, Chung HM, Lee DR. Effect of human endothelial progenitor cell (EPC)- or mouse vascular endothelial growth factor-derived vessel formation on the survival of vitrified/warmed mouse ovarian grafts. Reprod Sci. 2014;21(7):859–68.
Johnson J, Canning J, Kaneko T, Pru JK, Tilly JL. Germline stem cells and follicular renewal in the postnatal mammalian ovary. Nature. 2004;428(6979):145–50.
Morita Y, Perez GI, Maravei DV, Tilly KI, Tilly JL. Targeted expression of Bcl-2 in mouse oocytes inhibits ovarian follicle atresia and prevents spontaneous and chemotherapy-induced oocyte apoptosis in vitro. Mol Endocrinol. 1999;13(6):841–50.
Bachelot A, Nicolas C, Bidet M, Dulon J, Leban M, Golmard JL, Polak M, Touraine P. Long-term outcome of ovarian function in women with intermittent premature ovarian insufficiency. Clin Endocrinol. 2017;86(2):223–8.
Rossouw JE, Anderson GL, Prentice RL, LaCroix AZ, Kooperberg C, Stefanick ML, Jackson RD, Beresford SA, Howard BV, Johnson KC, et al. Risks and benefits of estrogen plus progestin in healthy postmenopausal women: principal results from the Women’s Health Initiative randomized controlled trial. JAMA. 2002;288(3):321–33.
Trounson A, McDonald C. Stem cell therapies in clinical trials: progress and challenges. Cell Stem Cell. 2015;17(1):11–22.
Song D, Zhong Y, Qian C, Zou Q, Ou J, Shi Y, Gao L, Wang G, Liu Z, Li H, et al. Human umbilical cord mesenchymal stem cells therapy in cyclophosphamide-induced premature ovarian failure rat model. Biomed Res Int. 2016;2016:2517514.
Elfayomy AK, Almasry SM, El-Tarhouny SA, Eldomiaty MA. Human umbilical cord blood-mesenchymal stem cells transplantation renovates the ovarian surface epithelium in a rat model of premature ovarian failure: possible direct and indirect effects. Tissue Cell. 2016;48(4):370–82.
Maas SLN, Breakefield XO, Weaver AM. Extracellular vesicles: unique intercellular delivery vehicles. Trends Cell Biol. 2017;27(3):172–88.
Yeo RW, Lai RC, Zhang B, Tan SS, Yin Y, Teh BJ, Lim SK. Mesenchymal stem cell: an efficient mass producer of exosomes for drug delivery. Adv Drug Deliv Rev. 2013;65(3):336–41.
Liang X, Ding Y, Zhang Y, Tse HF, Lian Q. Paracrine mechanisms of mesenchymal stem cell-based therapy: current status and perspectives. Cell Transplant. 2014;23(9):1045–59.
Bi B, Guo J, Marlier A, Lin SR, Cantley LG. Erythropoietin expands a stromal cell population that can mediate renoprotection. Am J Physiol Renal Physiol. 2008;295(4):F1017–22.
Detti L, Uhlmann RA, Zhang J, Diamond MP, Saed GM, Fletcher NM, Lu M, Williams LJ. Goserelin fosters bone elongation but does not prevent ovarian damage in cyclophosphamide-treated prepubertal mice. Fertil Steril. 2014;101(4):1157–64 e1151.
Ezoe K, Murata N, Yabuuchi A, Okuno T, Kobayashi T, Kato O, Kato K. Long-term adverse effects of cyclophosphamide on follicular growth and angiogenesis in mouse ovaries. Reprod Biol. 2014;14(3):238–42.
Kamat BR, Brown LF, Manseau EJ, Senger DR, Dvorak HF. Expression of vascular permeability factor vascular endothelial growth factor by human granulosa and theca lutein cells. Am J Pathol. 1995;146:157–65.
Robinson RS, Woad KJ, Hammond AJ, Laird M, Hunter MG, Mann GE. Angiogenesis and vascular function in the ovary. Reproduction. 2009;138(6):869–81.
Chen J, Liu Z, Hong MM, Zhang H, Chen C, Xiao M, Wang J, Yao F, Ba M, Liu J, et al. Proangiogenic compositions of microvesicles derived from human umbilical cord mesenchymal stem cells. PLoS One. 2014;9(12):e115316.
Shin SY, Lee JY, Lee E, Choi J, Yoon BK, Bae D, Choi D. Protective effect of vascular endothelial growth factor (VEGF) in frozen-thawed granulosa cells is mediated by inhibition of apoptosis. Eur J Obstet Gynecol Reprod Biol. 2006;125(2):233–8.
Mao J, Smith MF, Rucker EB, Wu GM, McCauley TC, Cantley TC, Prather RS, Didion BA, Day BN. Effect of epidermal growth factor and insulin-like growth factor I on reantral follicular growth, antrum formation, and stimulation of granulosal cell porcine proliferation and suppression of apoptosis in vitro. J Anim Sci. 2004;82:1967–75.
Sharma GT, Dubey PK, Kumar GS. Effects of IGF-1, TGF-alpha plus TGF-beta1 and bFGF on in vitro survival, growth and apoptosis in FSH-stimulated buffalo (Bubalis bubalus) preantral follicles. Growth Hormon IGF Res. 2010;20(4):319–25.
Xia X, Yin T, Yan J, Yan L, Jin C, Lu C, Wang T, Zhu X, Zhi X, Wang J, et al. Mesenchymal stem cells enhance angiogenesis and follicle survival in human cryopreserved ovarian cortex transplantation. Cell Transplant. 2015;24(10):1999–2010.
Jia X, Pan J, Li X, Li N, Han Y, Feng X, Cui J. Bone marrow mesenchymal stromal cells ameliorate angiogenesis and renal damage via promoting PI3k-Akt signaling pathway activation in vivo. Cytotherapy. 2016;18(7):838–45.
Zheng W, Nagaraju G, Liu Z, Liu K. Functional roles of the phosphatidylinositol 3-kinases (PI3Ks) signaling in the mammalian ovary. Mol Cell Endocrinol. 2012;356(1–2):24–30.
Hung SC, Pochampally RR, Chen SC, Hsu SC, Prockop DJ. Angiogenic effects of human multipotent stromal cell conditioned medium activate the PI3K-Akt pathway in hypoxic endothelial cells to inhibit apoptosis, increase survival, and stimulate angiogenesis. Stem Cells. 2007;25(9):2363–70.
The authors thank Reproductive Medicine Center, Cell Therapy Center, and Department of Pathology of 105th Hospital of the People’s Liberation Army. The authors are grateful to all members of the Reproductive Medicine Center of the 105th Hospital of PLA.
This work was supported by the Science and Technology Innovation Project of Nanjing Military Region (grant number 14ZX06 and 11Z010).
Ethics approval and consent to participate
The experimental protocol about animals and the collection of the samples used for research purposes in this study were approved by the Ethical Committee and the Institutional Animal Care and Use Committee of Anhui Medical University.
Consent for publication
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Yang, Z., Du, X., Wang, C. et al. Therapeutic effects of human umbilical cord mesenchymal stem cell-derived microvesicles on premature ovarian insufficiency in mice. Stem Cell Res Ther 10, 250 (2019). https://doi.org/10.1186/s13287-019-1327-5
- Mesenchymal stem cells (MSCs)
- Microvesicles (MVs)
- Premature ovarian insufficiency (POI)