Int J Med Sci 2012; 9(7):592-602. doi:10.7150/ijms.4841
CD44+/CD105+ Human Amniotic Fluid Mesenchymal Stem Cells Survive and Proliferate in the Ovary Long-Term in a Mouse Model of Chemotherapy-Induced Premature Ovarian Failure
1. Shanghai Geriatric Institute of Chinese Medicine, Longhua Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai 200031, China;
2. International Peace Maternity and Child Health Hospital, Shanghai Jiaotong University, Shanghai 200030, China;
3. Institute of Biochemistry and Cell Biology, Shanghai Institute for Biological Sciences, Chinese Academy of Sciences, Shanghai 200031, China;
4. Shanghai First Maternity and Infant Hospital, Tongji University School of Medicine, Shanghai 200040, China;
5. Sino-America United Stem Cell Research Center, Shanghai 200333, China.
Liu T, Huang Y, Guo L, Cheng W, Zou G. CD44+/CD105+ Human Amniotic Fluid Mesenchymal Stem Cells Survive and Proliferate in the Ovary Long-Term in a Mouse Model of Chemotherapy-Induced Premature Ovarian Failure. Int J Med Sci 2012; 9(7):592-602. doi:10.7150/ijms.4841. Available from http://www.medsci.org/v09p0592.htm
Objectives: Stem cell transplantation has been reported to rescue ovarian function in a preclinical mouse model of chemotherapy-induced premature ovarian failure (POF); however, maintaining the survival and self-renewal of transplanted seed cells in ovarian tissues over the long-term remains a troublesome issue. In this study we aimed to determine whether the CD44+/CD105+ human amniotic fluid cell (HuAFCs) subpopulation represent potential seed cells for stem cell transplantation treatments in POF. Materials and methods: The CD44+/CD105+ subpopulation were isolated from HuAFCs, cultured in vitro, and injected into a cyclophosphamide-induced mouse model of POF. Results: Under continuous subculture in vitro, CD44+/CD105+ cells proliferated rapidly and expressed high levels of the proliferative markers Ki67 and survivin, as well as high levels of a number of mesenchymal stem cell biomarkers. Moreover, when red fluorescence protein (RFP)-transduced CD44+/CD105+ HuAFCs were transplanted into the ovaries of POF mice, the cells could be detected by fluorescence microscopy up to three weeks after injection. Furthermore, the BrdUrd incorporation assay and immunofluorescent staining demonstrated that CD44+/CD105+ HuAFCs underwent normal cycles of cell proliferation and self-renewal in the ovarian tissues of POF mice over the long-term. Conclusions: The mesenchymal stem cell properties and long-term in vivo survival of CD44+/CD105+ HuAFCs make them ideal seed cells for stem cell transplantation to treat POF.
Keywords: Mouse premature ovarian failure model, cell transplantation, human amniotic fluid cells, mesenchymal stem cell like cells, long-term survival, proliferation.
Increasing attention is being paid to premature ovarian failure (POF), which is one of the most threatening diseases to female reproductive health. Approximately 1-5% of women worldwide experience cessation of their menstrual cycle prior to age 40, a condition known as POF [1-8]. Patients with POF have a number of typical characteristics [6, 7]: (a) primary or secondary amenorrhea; (b) at least intermittent hypoestrogenism; (c) hypergonadotropinism; and (d) age under 40 years at the time of onset. In some patients with POF, laparoscopy reveals a lack of developing follicles and ovarian biopsy shows a network of connective tissue interspersed with fibroblasts. The uterus and vaginal mucosa undergo atrophy in patients with POF, due to a lack of estrogen stimulation from the inactive ovaries [2, 3]. The incidence of POF has increased in recent years. Although some treatments are currently available, the condition cannot be reversed, and it would be desirable to find improved therapeutic strategies for POF.
Human amniotic fluid cells (HuAFCs) are currently used for the routine prenatal genetic diagnosis of a wide range of foetal abnormalities [9, 10]. However, amniotic fluid contains multiple types of cells derived from the developing foetus. These cells can differentiate into a variety of cell types, including adipose, muscle, bone and neuronal cells [11, 12]. The CD44+/CD105+ subpopulation can be directly sorted from human amniotic fluid and cultured for ex vivo expansion [13-17]. Previous studies have demonstrated the ability of CD44+/CD105+ cells to differentiate into ectodermal, endodermal, mesodermal, hepatic cells and cardiac muscle cells ; therefore, the CD44+/CD105+ human amniotic fluid subpopulation can differentiate into all three germ layers. Additionally, our previous studies indicated that HuAFCs express a variety of growth factors, including epidermal growth factor (EGF), basic fibroblast growth factor (bFGF), transforming growth factor alpha (TGF-α), transforming growth factor beta (TGF-β) and bone morphogenetic protein 4 (BMP-4), as well as the stem cell markers Nanog, Oct4 and Nestin. More importantly, HuAFCs lack major histocompatibility complex class II antigens and express only low levels of major histocompatibility complex class I antigens [18-21]. Indeed, we have reported that dopaminergic neuron-like cells derived from CD44+ HuAFCs were ameliorative to behavioural recovery in a rat model of Parkinson's disease, and also that CD44+/CD105+ HuAFCs could be induced to differentiate into pancreatic β-cell-like cells [19-21]. HuAFCs cells are more easily accessible than other adult stem cells, making them a potential autologous donor source for stem cell therapy. Therefore, in this study we aimed to determine which subpopulations of HuAFCs can survive and proliferate in vitro and in vivo, and investigated whether the CD44+/CD105+ HuAFC subpopulation have the properties of mesenchymal stem cells and represent potential seed cells for stem cell transplantation to treat POF.
Materials and Methods
Isolation and in vitro expansion of CD44 and CD105 phenotype cells by magnetic activated cell sorting system
Human amniotic fluids were obtained by ultrasound-guided amniocentesis performed on pregnant women for routine prenatal diagnosis purposes at gestational ages ranging from 18 th -22th weeks. All of the 10 human samples were obtained after approval from the Ethical Review Board of the Shanghai First Maternity and Infant Hospital (Shanghai, China) and after obtaining written informed consent from subjects. CD44+/CD105+ subpopulation cells were isolated from those human amniotic fluid using 4μl of the primary monoclonal antibodies (mouse anti-human CD44-FITC, rabbit anti-human CD105-PE, eBioscience Inc, San Diego, CA, USA)) stored at 4℃ in PBS for 30 min in a volume of 1ml as previously described [17-21]. After reaction, the cells were washed twice in PBS, and were put the secondary monoclonal antibodies (Goat anti-mouse or Goat anti-rabbit coupled to magnetic microbeads, Miltenyi Biotec, Auburn, CA), incubated at 10℃ in PBS for 15 min and then washed twice in PBS. The subpopulation cells were plated at 1×106 cells/ml in DMEM:F12 (1:1) (Gibco, Gaithersburg, MD, USA), supplemented with 10ng/ml basic fibroblast growth factor (bFGF), 10ng/ml epidermal growth factor (EGF) (all from Sigma-Aldrich, St Louis, USA), 10% fetal bovine serum and 2mM L-glutamine (all from Gibco, Gaithersburg, MD, USA). All CD44+CD105+ cells were cultured in a humidified incubator, at 37℃ with 5%CO2, until 80% confluent. In this experiment, all cells had been cultured on the same conditions until passage 4th before making ulterior experiments.
MTT assay for cell proliferation
Each group of cells was seeded at 2 × 103 cells per well in 96-well plates, and cultured in DMEM:F12 (1:1) supplemented with 10% fetal bovine serum at 37 ℃ with 5% CO2, until 85% confluence had been reached. MTT (Sigma-Aldrich, St Louis, USA) (5 mg/mL) was added to the maintenance cell medium at different time points, and incubated at 37 ℃ for an additional 4h. The reaction was terminated with 150 μL of dimethylsulfoxide (Sigma-Aldrich, St Louis, USA) per well, the cells were lysed for 15 min, and the plates were gently shaken for 5 min. Absorbance values were determined with an ELISA reader (Model 680; Bio-Rad, Hercules, CA, USA) at 490 nm.
RNA extraction and analysis by quantitative real-time PCR
Total RNA from each cell was isolated with Trizol Reagent (Invitrogen, Life Technologies Corporation, Grand Island, NY, USA), according to the manufacturer's protocol. The RNA samples were treated with DNase I (Sigma-Aldrich, St Louis, USA), quantified, and reverse-transcribed into cDNA with the ReverTra Ace- First Strand cDNA Synthesis Kit (TOYOBO, TOYOBO (SHANGHAI) BIOTECH CO., LTD., Shanghai, China). Quantitative real-time PCR was conducted with a RealPlex4 real-time PCR detection system from Eppendorf (Germany), with SyBR Green RealTime PCR Master Mix (TOYOBO, TOYOBO (SHANGHAI) BIOTECH CO., LTD., Shanghai, China) as the detection dye. Quantitative real-time PCR amplification was performed over 40 cycles with denaturation at 95 °C for 15 s and annealing at 58 °C for 45 s. Target cDNA was quantified with the relative quantification method. A comparative threshold cycle (Ct) was used to determine gene expression relative to a control (calibrator), and steady-state mRNA levels are reported as an n-fold difference relative to the calibrator. For each sample, the maker gene Ct values were normalized with the formula ΔCt = Ct_genes - Ct_18S RNA. To determine relative expression levels, the following formula was used: ΔΔCt = ΔCt_all_groups - ΔCt_blankcontrol_group. The values used to plot relative expressions of markers were calculated with the expression 2−ΔΔCt. The mRNA levels were calibrated on the basis of levels of 18S rRNA. The cDNA of each gene was amplified with primers as previously described: Ki67-FP: TGGGTCTGTTATTGATGAGCC; Ki67-RP: TGACTTCCTTCCATTCTGAAGAC; Survivin-FP: TTGGTGAATTTTTGAAACTGGA; Survivin-RP: CTTTCTCCGCAGTTTCCTCA; 18SrRNA-FP: CGTTGATTAAGTCCCTGCCCTT; 18SrRNA-RP: TCAAGTTCGACCGTCTTCTCAG.
Western blotting analysis
Cells were lysed using a 2 × loading lysis buffer (50 mM Tris-HCl, pH 6.8, 2% sodium dodecyl sulfate, 10% β-mercaptoethanol, 10% glycerol and 0.002% bromophenol blue). The total amount of proteins from the cultured cells was subjected to 12% SDS-PAGE and transferred onto Hybrid-PVDF membrane (Millipore, Bedford, USA) membranes. After blocking with 5% (w/v) non-fat dried milk in TBST (Tris-buffered saline containing Tween-20) (25 mM Tris/HCl, pH 8.0, 125 mM NaCl and 0.05% Tween-20), the PVDF membranes were washed 4 times (15 min each) with TBST at room temperature and incubated with primary antibody (rabbit anti-human Ki67 polyclonal antibody (1:1000; Chemicon, Temecula, CA, USA) and rabbit anti-human Survivin polyclonal antibody (1:1000; Chemicon, Temecula, CA, USA)). Following extensive washing, membranes were incubated with HRP-conjugated goat anti-rabbit IgG secondary antibody (1:1000; Santa Cruz Technology, Santa Cruz, USA) for 1 h. After washing 4 times (15 min each) with TBST at room temperature, the immunoreactivity was visualized by enhanced chemiluminescence using ECL kit from Perkin-Elmer Life Science (Norwalk, USA).
The cultured cells were washed 3 times with PBS and fixed with 4% paraformaldehyde (Sigma-Aldrich, St. Louis, USA) for 30 min. After blocking, the cells were incubated first with rabbit anti-human Ki67 polyclonal antibody (1:200; Chemicon, Temecula, CA, USA) and rabbit anti-BrdU polyclonal antibody (1:200; Sigma-Aldrich, St Louis, USA) overnight at 4 °C, and then with FITC-conjugated goat anti-rabbit IgG antibody (1:200; Sigma-Aldrich, St Louis, USA) and 5 μg/ml DAPI (Sigma-Aldrich, St Louis, USA) at room temperature for 30 min. Then the cells were thoroughly washed with TBST and viewed through a fluorescence microscope (DMI3000; Leica, Allendale, NJ, USA).
The mouse model of premature ovarian failure and xenografing experiments
Hebetic femal C57BL/6 mice (n = 12), between 4 and 5 weeks of age, obtained from the Shanghia Tongji University with Institutional Anminal Care and Use Committer approval in accordance with institutional guidelines. All mice were maintained for 14 days, 3 to 4 per cage, in a temperature controlled coloney room under standard light-dark cycle with free access to food and water. The study protocol was according the manuscript  and had some ameliorations. To build the POF model, mice were administered single intraperitoneal injection of 70 mg/kg cyclophosphamide (Sigma-Aldrich, St Louis, USA) at 6 weeks of age. The animals were divided into 2 groups: a negative control groups (6 animals of POF model) grafted with CD44-/CD105- HuAFCs in right ovarian, and an experimental group (6 animals of POF model) grafted with CD44+/CD105+ HuAFCs in in right ovarian. One weeks after mouse POF model built successfully, each experimental model received an injection of 10μl of HuAFCs (approximately 1×103 cell spheres/μl), which was harbored a red fluorescence dye (DiIC18(3), 1'-dioctadecyl-3,3,3',3'-tetramethylindocarbocyanine perchlorate) , or PBS. The ulterior experiments of the animals model in both groups on 7, 14 and 21 day after transplantation.
The mouse estradiol (E2) and follicle stimulating hormone (FSH) ELISA kit (Westang Bio, Shanghai, China) was used according to the protocol description to determin the level of E2 or FSH in mouse plasma. Briefly, 100 μl of mouse E2 or FSH standards at concentrations of 0, 50, 300, 1000 and 5000 pg/ml or 0, 5, 10, 25, 50 and 100 mIU/ml or diluted mouse plasma were added to anti-E2 or FSH antibody precoated microtest wells and incubated for 60 min. After 3 times wash, the HRP-conjugated detection antibodies were then added followed by addition of the substrate solution. The absorbance was determined at a wavelength of 450 nm.
Flow cytometric (FCM) analysis of cell cycle by PI staining
Each group cells was seeded at 3×105 per well in 6-well plates and cultrued until 85% confluent. Each group cells was washed by PBS on three times, then were collected by centifugation (Allegra X-22R, Beckman Coulter) at 1000g for 5min. The cell pellets were the resuspended in 1mL of PBS, fixed in 70% ice-cold ethanol, and ketp in a freezer more than 48h. Before flow cytometric analysis, The fixed cells were centrifuged, washed twice with PBS, and resuspended in PI staining solution (Sigma Chemicals) containing 50μL/mL PI and 250μg/mL RNase A (Sigma Chemicals). The cell suspension, which was hidden from light, were incubated for 30min at 4℃ and analyzed using the FACS (FCM-500, Beckman Coulter). A total of 10,000 events were acquired for analysis using CellQuest software.
Each experiment was performed as least three times, and data are shown as the mean ± standard error where applicable; differences were evaluated with Student's t-tests. A p-value of < 0.05 was considered to be statistically significant.
Isolation and enrichment of the CD44+/CD105+ subpopulation from human amniotic fluid
Multiple cell types can be isolated from human amniotic fluid. Microscopy revealed that various different colonies formed after HuAFCs were cultured for 10 days in vitro (Figure 1). Previous studies have suggested that the CD44 and CD105-expressing cell subpopulation in human amniotic fluid is relatively small. Therefore, we used a magnetic activated cell sorting system to isolate and enrich this specific subpopulation. The cells were detected by flow cytometry (FCM), and CD44+/CD105+ cells represented 1.75% ± 0.25% of HuAFCs (Figure 1), indicating that CD44+/CD105+ cells could be successfully enriched from human amniotic fluid using magnetic activated cell sorting. Moreover, the CD44+/CD105+ HuAFCs had remarkable morphological differences compared to the remaining HuAFC subpopulation. CD44+/CD105+ HuAFCs had a typical mesenchymal morphology; whereas CD44-/CD105- HuAFCs were spindle-shaped or polygonal, and retained a cobblestone appearance (Figure 1).
CD44+/CD105+ HuAFCs proliferate rapidly and express high levels of mesenchymal stem cell biomarkers
The MTT assay was used to determine the viability of CD44+/CD105+ and CD44-/CD105- HuAFCs at the same passage over time in vitro. There was no significant difference in the viability of CD44+/CD105+ HuAFCs and CD44-/CD105- HuAFCs at 24 h after isolation; however, the viability of CD44-/CD105- HuAFCs significantly reduced at 2 d and 5 d compared to CD44+/CD105+ HuAFCs (Figure 2), indicating that CD44+/CD105+ HuAFCs proliferated more rapidly than CD44-/CD105- HuAFCs (Table 1). FCM indicated that CD44-/CD105- HuAFCs were arrested in the G2/M phase of the cell cycle, with a significantly reduced percentage of S phase cells (Table 2); whereas CD44+/CD105+ HuAFCs displayed a normal cell cycle distribution and underwent cell division (Figure 2). To confirm that CD44+/CD105+ HuAFCs proliferated in vitro, the expression of proliferation-related markers were assayed by quantitative real-time polymerase chain reaction (qRT-PCR) and Western blotting. The relative expression levels of several important proliferation-related markers were compared using qRT-PCR, and normalized to the internal control 18S rRNA. Ki67 and survivin mRNA were expressed at significantly higher levels in CD44+/CD105+ HuAFCs than CD44-/CD105- HuAFCs (Figure 2). Western blotting confirmed that Ki67 and survivin were expressed at significantly higher levels in CD44+/CD105+ HuAFCs (1.000 ± 0.056 and 1.000 ± 0.035) than CD44-/CD105- HuAFCs (0.229 ± 0.054 and 0.339 ± 0.049 relative to GAPDH levels, respectively; Figure 2).
In order to evaluate the degree of mesenchymal stem cell "stemness" in the CD44+/CD105+ and CD44-/CD105- HuAFC subpopulations, we analyzed the expression of several mesenchymal stem cell biomarkers using FCM (Figure 2). Expression of the "stemness" markers CD29, CD44, CD73, CD90, CD105 and CD166 was approximately 60- to 90-fold higher in CD44+/CD105+ HuAFCs than CD44-/CD105- HuAFCs, suggesting that the CD44+/CD105+ subpopulation possess more of the properties of mesenchymal stem cells than the CD44-/CD105- subpopulation.
Establishment of a mouse model of chemotherapy-induced premature ovarian failure
In order to evaluate whether the mouse POF model was established successfully, the plasma E2 and FSH levels and ovarian pathology were investigated. After injection of cyclophosphamide, the plasma E2 and FSH levels reduced over time in the POF mouse model group, but not in the normal health mouse. ELISA assays indicated that the POF mouse models lacked hormonal maintenance from the ovaries (Figure 3). In addition, ovarian pathology revealed that the ovaries of the health normal health mouse ontained a large number of follicles at all stages of immaturity or maturation (Figure 3). In contrast, the atrophied ovaries of the POF model mice were mostly composed of interstitial cells in a fibrous matrix, with a reduced number of follicles at each stage. Additionally, the ovaries of the POF model mice contained an increased number of collapsed oocytes (Figure 3).
MTT assay determination of the viability of HuAFCs in vitro
|Day||CD44+/CD105+ HuAFCs (n = 3)||CD44-/CD105- HuAFCs (n = 3)|
Mesenchymal stem cell biomarkers expression of HuAFCs determined by FCM
|Cells||CD29 (%)||CD44 (%)||CD73 (%)||CD90 (%)||CD105 (%)||CD166 (%)|
Isolation and characterisation of the different subpopulations of cells in human amniotic fluid. (A) Multiple cell populations exist in human amniotic fluid. (a), (b) and (c) illustrate the morphology of different cell subpopulations in human primary amniotic fluid. Original magnification, 200×. (B) Morphology of the CD44+/CD105+ subpopulation isolated from human primary amniotic fluid. Original magnification, 200×. (C) Morphology of the CD44-/CD105- subpopulation isolated from human primary amniotic fluid. Original magnification, 200×. (D) Isolation of CD44+/CD105+ HuAFCs from amniotic fluid. The cells were detected by FCM; CD44+/CD105+ cells represented 1.75% ± 0.25% of the HuAFC population.(Click on the image to enlarge.)
Analysis of the proliferation and survival of CD44+/CD105+ HuAFCs in vitro. (A) MTT assays indicated that the viability of CD44-/CD105- HuAFCs significantly reduced at both 2 d and 5 d, compared to CD44+/CD105+ HuAFCs. **P < 0.01 vs. CD44-/CD105- HuAFCs; *P < 0.05 vs. CD44-/CD105- HuAFCs; #P > 0.05 vs. CD44-/CD105- HuAFCs; n = 3. (B) qRT-PCR analysis of Ki67 and survivin mRNA expression in CD44+/CD105+ and CD44-/CD105- HuAFCs; *P < 0.05 vs. CD44-/CD105- HuAFCs; #P > 0.05 vs. CD44-/CD105- HuAFCs; n = 3. (C) Western blotting analysis of Ki67 and survivin protein expression in CD44+/CD105+ and CD44-/CD105- HuAFCs; **P < 0.01 vs. CD44+/CD105+ HuAFCs; * P< 0.05 vs. CD44+/CD105+ HuAFCs; #P > 0.05 vs. CD44+/CD105+ HuAFCs; n = 3. (D) Flow cytometric cell cycle analysis of CD44+/CD105+ and CD44-/CD105- HuAFCs. The majority of CD44-/CD105- HuAFCs were arrested in the G2/M phase with a reduced percentage of S phase cells; **P < 0.01 vs. CD44+/CD105+ HuAFCs; *P < 0.05 vs. CD44+/CD105+ HuAFCs; #P > 0.05 vs. CD44+/CD105+ HuAFCs; n = 3. (E) FCM analysis of human mesenchymal stem cell marker expression in CD44+/CD105+ and CD44-/CD105- HuAFCs in vitro. Expression of the "stemness" markers was higher in CD44+/CD105+ HuAFCs than CD44-/CD105- HuAFCs.(Click on the image to enlarge.)
CD44+/CD105+ HuAFCs survive and proliferate in the ovaries of the POF model mice
Red fluorescent protein (RFP)-expressing HuAFCs were injected in vivo and the ovary injection tracts were examined after one, two and three weeks to confirm the presence of transplanted HuAFCs. As anticipated, RFP-positive CD44+/CD105+ HuAFCs could be observed along the injection tract after one, two and three weeks in the ovaries of mice from the POF model (Figure 4), demonstrating that the transplanted CD44+/CD105+ HuAFCs could survive within the POF mouse ovaries for at least three weeks in vivo. and morphological change can be seen after that. RFP-positive CD44-/CD105- HuAFCs could not be found along the injection tract in the ovaries of mice from the POF model, confirming that only grafted CD44+/CD105+ HuAFCs survived in vivo.
In addition, analysis of cell proliferation using FCM revealed that the number of CD44+/CD105+ HuAFCs elevated appreciably in vivo from the time of the graft to three weeks after transplantation (Figure 5), whereas RFP-transduced CD44-/CD105- HuAFCs could not be detected by FCM. Furthermore, BrdUrd incorporation and IF staining revealed that transplanted CD44+/CD105+ HuAFCs had a normal cell cycle distribution and underwent cell division in vivo (Figure 5).
Establishment of a mouse model of POF. (A, B) Ovarian pathology of the wt group (A) and POF group (B) at 2 weeks after injection of cyclophosphamide. The ovaries of the wt group and vehicle group contained a large number of follicles at all stages of immaturity or maturation; whereas the atrophied ovaries of the POF model mice were mostly composed of interstitial cells in a fibrous matrix, with a reduced number of follicles at each stage and an increased number of collapsed oocytes. Original magnification, 100×. (C, D) Plasma E2 levels (C) and FSH levels (D) as determined by ELISA at various time points after the injection of cyclophosphamide; **P < 0.01 vs. WT; #P > 0.05 vs. WT.(Click on the image to enlarge.)
HuAFCs survived in vivo in the ovary in a mouse model of POF. Immunofluorescence (IF) demonstrated that Dil, a marker of HuAFCs, was expressed at high levels in grafted CD44+/CD105+ HuAFCs transplanted into POF mouse ovaries; the transplanted cells survived for at least three weeks in vivo. In addition, BrdUrd incorporation and IF staining indicated that transplanted CD44+/CD105+ HuAFCs underwent normal cell division. CD44-/CD105- HuAFCs could not be detected along the injection tract in POF mouse ovaries. Original magnification: ×200.(Click on the image to enlarge.)
HuAFCs proliferated in vivo in the ovary in a mouse model of POF. Immunofluorescent staining and FCM indicated that the number of Dil positive (red, a marker of HuAFCs) CD44+/CD105+ HuAFCs increased from the time of the graft up to three weeks after transplantation. RFP-transduced CD44-/CD105- HuAFCs could not be detected. **P < 0.01 vs. CD44-/CD105- HuAFCs; *P < 0.05 vs. CD44-/CD105- HuAFCs; n = 3.(Click on the image to enlarge.)
Premature ovarian failure (POF), a condition which causes amenorrhoea and hypergonadotropic hypoestrogenism before the age of 40, affects 1% of women in the general population [1, 2, 7, 8]. The occurrence of POF has increased in recent years. As yet, POF cannot be reversed and though some treatments are currently available, improved treatment strategies are urgently required. Regenerative medicine research suggests that stem cells could be used to treat various human diseases, due to their self-renewal capacity and multiplex differentiation potential. In view of this idea, it is possible that suitable stem cells could be used to treat POF. In our previous studies, we observed that CD44+/CD105+ human amniotic fluid cells (HuAFCs) express a variety of growth factors, lack major histocompatibility complex class II antigens and express only low levels of major histocompatibility complex class I antigens. Furthermore, we previously demonstrated that CD44+/CD105+ HuAFCs can be induced to differentiate into somatic cells [19-21]. Therefore, we hypothesised that CD44+/CD105+ HuAFCs could potentially be used to treat POF. Stem cell transplantation has been reported to rescue ovarian function in a preclinical mouse model of chemotherapy-induced premature ovarian failure (POF) . However, maintaining the survival and self-renewal of seed cells in ovarian tissues over the long-term remains a troublesome issue. In this study, we aimed to determine whether the CD44+/CD105+ HuAFC subpopulation could survive and proliferate in vitro and in vivo over the long-term.
CD44+/CD105+ HuAFCs were successfully enriched from human amniotic fluids using magnetic activated cell sorting. Thereafter, the CD44+/CD105+ and CD44-/CD105- HuAFCs were cultured under the same conditions, and their “stemness” properties and proliferation rates were compared. MTT assays indicated that the viability of CD44-/CD105- HuAFCs significantly reduced on day 3 in vitro, in contrast to CD44+/CD105+ HuAFCs. BrdUrd incorporation and FCM confirmed that CD44+/CD105+ HuAFCs proliferated in vitro, but CD44-/CD105- HuAFCs did not. Western blotting and qRT-PCR showed that the levels of the proliferation markers Ki67 and survivin were significantly higher in CD44+/CD105+ HuAFCs than CD44-/CD105- HuAFCs. Furthermore, the expression levels of a number of "stemness" markers were higher in CD44+/CD105+ HuAFCs than CD44-/CD105- HuAFCs. Taken together, these results demonstrated that the CD44+/CD105+ subpopulation possesses more of the properties of mesenchymal stem cells than the CD44-/CD105- subpopulation. Next, the two subpopulations of cells were transplanted into the ovaries of a mouse model of POF. After three weeks, RFP-positive CD44+/CD105+ HuAFCs could be observed along the injection tract in the ovaries of the POF mice, however, RFP-positive CD44-/CD105- HuAFCs could not be detected, demonstrating that transplanted CD44+/CD105+ HuAFCs can survive within the POF mouse ovaries for at least three weeks in vivo. Additionally, FCM revealed that the number of CD44+/CD105+ HuAFCs increased appreciably between the time of the graft and three weeks after transplantation, while the RFP-transduced CD44-/CD105- HuAFCs could not be detected. BrdUrd incorporation and FCM confirmed that the transplanted CD44+/CD105+ HuAFCs underwent normal cell division and proliferation.
In conclusion, CD44+/CD105+ HuAFCs possess the characteristics of mesenchymal stem cells, and can survive and proliferate over the long term in the ovarian tissues of a mouse model of chemotherapy-induced POF.
This work was supported by grants from Shanghai Committee Medical Science Foundation of China (No.10411967100) and the Natural Science Foundation of School of Medicine of Shanghai Jiaotong University (No.YZ1046) to Te Liu.
The authors have declared that no competing interest exists.
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Corresponding author: Te Liu Ph.D., Shanghai Geriatric Institute of Chinese Medicine, Longhua Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai 200031, P.R. China, Phone: 86-21-64720010; Fax: 86-21-64720010; E-Mail: liute79com.