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Overexpression of CD61 promotes hUC-MSC differentiation into male germ-like cells.

Authors :
Li, Bo
Liu, Weishuai
Zhuang, Mengru
Li, Na
Wu, Siyu
Pan, Shaohui
Hua, Jinlian
Source :
Cell Proliferation. Feb2016, Vol. 49 Issue 1, p36-47. 12p.
Publication Year :
2016

Abstract

Objectives Previous studies have shown that germ-like cells can be induced from human umbilical cord mesenchymal stem cell ( hUC- MSCs) in vitro. However, induction efficiency was low and a stable system had not been built. CD61, also called integrin-β3, plays a significant role in cell differentiation, in that CD61-positive-cell-derived pluripotent stem cells easily differentiate into primordial germ-like cells ( PGC). Here, we have explored whether overexpression of CD61 would promote hUC- MSC differentiation into PGC and male germ-like cells. Materials and methods hUC- MSCs were cultured and transduced using pCD61- CAGG- TRIP-pur ( oCD61) and pTRIP- CAGG plasmid (Control), and hUC-MSCs overexpressed CD61 were induced by bone morphogenetic protein 4 ( BMP4, 12.5 ng/ml), to differentiate into PGC and male germ cells. Quantitative real-time PCR ( RT- qPCR), western blotting and immunofluorescence staining were used to examine PGC- and germ cell-specific markers. Results High expression levels of PGC-specific markers were detected in oCD61 hUC- MSCs compared to controls. After BMP4 induction, expression levels of male germ cell markers such as Acrosin (ACR), Prm1 and meiotic markers including Stra8, Scp3 in oCD61 were significantly higher than those of the Control group. Conclusions Under induction of BMP4, CD61-overexpressing hUC- MSCs, which had turned into PGC-like cells, could be further differentiated into male germ-like cells. Thus, a simple and efficient approach to study male germ cell development by using hUC- MSCs has been established. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09607722
Volume :
49
Issue :
1
Database :
Academic Search Index
Journal :
Cell Proliferation
Publication Type :
Academic Journal
Accession number :
112901936
Full Text :
https://doi.org/10.1111/cpr.12236