Proliferation and Differentiation of Mouse Spermatogonial Stem Cells on a Three-Dimensional Surface Composed of PCL/Gel Nanofibers
SUMMARY: Spermatogonial stem cells (SSCs) have self-renewal and differentiation capacity essential for sperm production throughout the male reproductive life. The electrospun polycaprolactone/gelatin (PCL/Gel) nanofibrous scaffold mimics important features of the extracellular matrix (ECM), which ca...
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Sociedad Chilena de Anatomía
2019
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oai:scielo:S0717-950220190003011322019-09-11Proliferation and Differentiation of Mouse Spermatogonial Stem Cells on a Three-Dimensional Surface Composed of PCL/Gel NanofibersTalebi,AliSadighi-Gilani,Mohammad AliKoruji,MortezaAi,JafarNavid,ShadanRezaie,Mohammad JafarJabari,AyobAshouri-Movassagh,SepidehKhadivi,FarnazSalehi,MajidHoshino,YumiAbbasi,Mehdi Adult germline stem cell Male infertility Cell differentiation Polycaprolactone Nanofibers SUMMARY: Spermatogonial stem cells (SSCs) have self-renewal and differentiation capacity essential for sperm production throughout the male reproductive life. The electrospun polycaprolactone/gelatin (PCL/Gel) nanofibrous scaffold mimics important features of the extracellular matrix (ECM), which can provide a promising technique for the proliferation and differentiation of SSCs in vitro. The goal of the present study was to investigate the effects of PCL/Gel nanofibrous scaffold on the propagation and differentiation of neonate mouse SSCs (mSSCs). mSSCs were enzymatically isolated, and the cells were purified by differential plating method and seeded on scaffold. After 2 weeks, viability, colony number and diameter, and expression of specific spermatogonial cell genes were investigated. After mSSCs propagation, the cells were cultivated in a differentiation medium on the scaffold for another 2 weeks, and differentiating cells were analyzed by real-time PCR. The number of mSSC colony (P<0.01) and expression levels of specific spermatogonial genes Plzf and Inga6 (P<0.01) and also differentiation genes c-Kit, Tp1 and Ptm1 (P<0.05) were higher in scaffold group compared with control during the culture period. We conclude that mSSCs can be expanded and can differentiate toward spermatid cells on PCL/Gel nanofibrous scaffold with improved developmental parameters.info:eu-repo/semantics/openAccessSociedad Chilena de AnatomíaInternational Journal of Morphology v.37 n.3 20192019-09-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-95022019000301132en10.4067/S0717-95022019000301132 |
institution |
Scielo Chile |
collection |
Scielo Chile |
language |
English |
topic |
Adult germline stem cell Male infertility Cell differentiation Polycaprolactone Nanofibers |
spellingShingle |
Adult germline stem cell Male infertility Cell differentiation Polycaprolactone Nanofibers Talebi,Ali Sadighi-Gilani,Mohammad Ali Koruji,Morteza Ai,Jafar Navid,Shadan Rezaie,Mohammad Jafar Jabari,Ayob Ashouri-Movassagh,Sepideh Khadivi,Farnaz Salehi,Majid Hoshino,Yumi Abbasi,Mehdi Proliferation and Differentiation of Mouse Spermatogonial Stem Cells on a Three-Dimensional Surface Composed of PCL/Gel Nanofibers |
description |
SUMMARY: Spermatogonial stem cells (SSCs) have self-renewal and differentiation capacity essential for sperm production throughout the male reproductive life. The electrospun polycaprolactone/gelatin (PCL/Gel) nanofibrous scaffold mimics important features of the extracellular matrix (ECM), which can provide a promising technique for the proliferation and differentiation of SSCs in vitro. The goal of the present study was to investigate the effects of PCL/Gel nanofibrous scaffold on the propagation and differentiation of neonate mouse SSCs (mSSCs). mSSCs were enzymatically isolated, and the cells were purified by differential plating method and seeded on scaffold. After 2 weeks, viability, colony number and diameter, and expression of specific spermatogonial cell genes were investigated. After mSSCs propagation, the cells were cultivated in a differentiation medium on the scaffold for another 2 weeks, and differentiating cells were analyzed by real-time PCR. The number of mSSC colony (P<0.01) and expression levels of specific spermatogonial genes Plzf and Inga6 (P<0.01) and also differentiation genes c-Kit, Tp1 and Ptm1 (P<0.05) were higher in scaffold group compared with control during the culture period. We conclude that mSSCs can be expanded and can differentiate toward spermatid cells on PCL/Gel nanofibrous scaffold with improved developmental parameters. |
author |
Talebi,Ali Sadighi-Gilani,Mohammad Ali Koruji,Morteza Ai,Jafar Navid,Shadan Rezaie,Mohammad Jafar Jabari,Ayob Ashouri-Movassagh,Sepideh Khadivi,Farnaz Salehi,Majid Hoshino,Yumi Abbasi,Mehdi |
author_facet |
Talebi,Ali Sadighi-Gilani,Mohammad Ali Koruji,Morteza Ai,Jafar Navid,Shadan Rezaie,Mohammad Jafar Jabari,Ayob Ashouri-Movassagh,Sepideh Khadivi,Farnaz Salehi,Majid Hoshino,Yumi Abbasi,Mehdi |
author_sort |
Talebi,Ali |
title |
Proliferation and Differentiation of Mouse Spermatogonial Stem Cells on a Three-Dimensional Surface Composed of PCL/Gel Nanofibers |
title_short |
Proliferation and Differentiation of Mouse Spermatogonial Stem Cells on a Three-Dimensional Surface Composed of PCL/Gel Nanofibers |
title_full |
Proliferation and Differentiation of Mouse Spermatogonial Stem Cells on a Three-Dimensional Surface Composed of PCL/Gel Nanofibers |
title_fullStr |
Proliferation and Differentiation of Mouse Spermatogonial Stem Cells on a Three-Dimensional Surface Composed of PCL/Gel Nanofibers |
title_full_unstemmed |
Proliferation and Differentiation of Mouse Spermatogonial Stem Cells on a Three-Dimensional Surface Composed of PCL/Gel Nanofibers |
title_sort |
proliferation and differentiation of mouse spermatogonial stem cells on a three-dimensional surface composed of pcl/gel nanofibers |
publisher |
Sociedad Chilena de Anatomía |
publishDate |
2019 |
url |
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-95022019000301132 |
work_keys_str_mv |
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