Supplementation of Glial Cell Line-Derived Neurotrophic Factor, Fibroblast Growth Factor 2, and Epidermal Growth Factor Promotes Self-Renewal of Putative Buffalo (Bubalus bubalis) Spermatogonial Stem Cells by Upregulating the Expression of miR-20b, miR-21, and miR-106a

In this study, we investigated the effect of glial cell line-derived neurotrophic factor (GDNF), fibroblast growth factor (FGF) 2, and epidermal growth factor (EGF) on the expression of some self-renewal-related microRNAs (miRs) in putative buffalo spermatogonial stem cells (SSCs). The SSCs were cul...

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Veröffentlicht in:Cellular reprogramming 2019-02, Vol.21 (1), p.11-17
Hauptverfasser: Sharma, Ankur, Lagah, Swati Viviyan, Nagoorvali, Dudekula, Kumar, B S Bharath, Singh, Manoj Kumar, Singla, Suresh Kumar, Manik, Radhay Sham, Palta, Prabhat, Chauhan, Manmohan Singh
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container_issue 1
container_start_page 11
container_title Cellular reprogramming
container_volume 21
creator Sharma, Ankur
Lagah, Swati Viviyan
Nagoorvali, Dudekula
Kumar, B S Bharath
Singh, Manoj Kumar
Singla, Suresh Kumar
Manik, Radhay Sham
Palta, Prabhat
Chauhan, Manmohan Singh
description In this study, we investigated the effect of glial cell line-derived neurotrophic factor (GDNF), fibroblast growth factor (FGF) 2, and epidermal growth factor (EGF) on the expression of some self-renewal-related microRNAs (miRs) in putative buffalo spermatogonial stem cells (SSCs). The SSCs were cultured on a buffalo Sertoli cell feeder layer, colony formation was observed between 7 and 10 days. The SSC colonies expressed markers specific for undifferentiated type A spermatogonia and pluripotency markers. After 15 days of initial culture, the colonies were subcultured as treatment (supplemented with 20 ng mL GDNF +10 ng mL FGF2 + 10 ng mL EGF) and control groups. The number and area of SSC colonies were significantly (p 
doi_str_mv 10.1089/cell.2018.0034
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The SSCs were cultured on a buffalo Sertoli cell feeder layer, colony formation was observed between 7 and 10 days. The SSC colonies expressed markers specific for undifferentiated type A spermatogonia and pluripotency markers. After 15 days of initial culture, the colonies were subcultured as treatment (supplemented with 20 ng mL GDNF +10 ng mL FGF2 + 10 ng mL EGF) and control groups. The number and area of SSC colonies were significantly (p &lt; 0.05) higher in the treatment group than in the control group. The relative abundance of miR-20b, miR-21, and miR-106a in SSCs supplemented with growth factors was significantly higher (p &lt; 0.001) than that in the control. 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The SSCs were cultured on a buffalo Sertoli cell feeder layer, colony formation was observed between 7 and 10 days. The SSC colonies expressed markers specific for undifferentiated type A spermatogonia and pluripotency markers. After 15 days of initial culture, the colonies were subcultured as treatment (supplemented with 20 ng mL GDNF +10 ng mL FGF2 + 10 ng mL EGF) and control groups. The number and area of SSC colonies were significantly (p &lt; 0.05) higher in the treatment group than in the control group. The relative abundance of miR-20b, miR-21, and miR-106a in SSCs supplemented with growth factors was significantly higher (p &lt; 0.001) than that in the control. 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The SSCs were cultured on a buffalo Sertoli cell feeder layer, colony formation was observed between 7 and 10 days. The SSC colonies expressed markers specific for undifferentiated type A spermatogonia and pluripotency markers. After 15 days of initial culture, the colonies were subcultured as treatment (supplemented with 20 ng mL GDNF +10 ng mL FGF2 + 10 ng mL EGF) and control groups. The number and area of SSC colonies were significantly (p &lt; 0.05) higher in the treatment group than in the control group. The relative abundance of miR-20b, miR-21, and miR-106a in SSCs supplemented with growth factors was significantly higher (p &lt; 0.001) than that in the control. The results indicate that supplementation of SSC culture medium with growth factors (GDNF, FGF2, and EGF) may promote the expression of miR-20b, miR-21, and miR-106a, which is essential for self-renewal and maintenance of SSCs.</abstract><cop>United States</cop><pmid>30589561</pmid><doi>10.1089/cell.2018.0034</doi><tpages>7</tpages></addata></record>
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title Supplementation of Glial Cell Line-Derived Neurotrophic Factor, Fibroblast Growth Factor 2, and Epidermal Growth Factor Promotes Self-Renewal of Putative Buffalo (Bubalus bubalis) Spermatogonial Stem Cells by Upregulating the Expression of miR-20b, miR-21, and miR-106a
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