Journal of Integrative Agriculture ›› 2013, Vol. 12 ›› Issue (10): 1839-1846.DOI: 10.1016/S2095-3119(13)60413-X

• 论文 • 上一篇    下一篇

ALK Family Inhibitor A83-01 Promotes the Proliferation of Mouse Male Germline Stem Cells (mGSCs) Under Serum- and Feeder-Free Conditions

 YU Meng, WANG Long, HU Yue, LIAN Zhi-min , HUA Jin-lian   

  1. College of Veterinary Medicine, Shaanxi Centre of Stem Cells Engineering & Technology/Key Lab for Animal Biotechnology, Agriculture Ministry of China/Northwest A&F University, Yangling 712100, P.R.China
  • 收稿日期:2012-07-18 出版日期:2013-10-01 发布日期:2013-10-01
  • 通讯作者: Correspondence HUA Jin-lian, Tel: +86-29-87080068, Fax: +86-29-87080068, E-mail: jinlianhua@nwsuaf.edu.ttcn, jlhua2003@126.com
  • 基金资助:

    This work is supported by grants from the National Natural Science Foundation of China, China (30972097, 31272518), the Program for New Century Excellent Talents in University, China (NCET-09-0654), and the Fundamental Research Funds for the Central Universities, China (QN2011012).

ALK Family Inhibitor A83-01 Promotes the Proliferation of Mouse Male Germline Stem Cells (mGSCs) Under Serum- and Feeder-Free Conditions

 YU Meng, WANG Long, HU Yue, LIAN Zhi-min , HUA Jin-lian   

  1. College of Veterinary Medicine, Shaanxi Centre of Stem Cells Engineering & Technology/Key Lab for Animal Biotechnology, Agriculture Ministry of China/Northwest A&F University, Yangling 712100, P.R.China
  • Received:2012-07-18 Online:2013-10-01 Published:2013-10-01
  • Contact: Correspondence HUA Jin-lian, Tel: +86-29-87080068, Fax: +86-29-87080068, E-mail: jinlianhua@nwsuaf.edu.ttcn, jlhua2003@126.com
  • Supported by:

    This work is supported by grants from the National Natural Science Foundation of China, China (30972097, 31272518), the Program for New Century Excellent Talents in University, China (NCET-09-0654), and the Fundamental Research Funds for the Central Universities, China (QN2011012).

摘要: A83-01 is a selective inhibitor of the TGF-β type I receptor ALK, which inhibits the TGF-β-induced epithelial-to-mesenchymal transition (EMT) via the inhibition of Smad2 phosphorylation. Previous studies have showed that A83-01 promoted somatic cellular reprogramming significantly. Male germline stem cells (mGSCs), as an alternative resource of pluripotent stem cells derived adult testis, have promising valuable in clinic medicine and regeneration, however, the derivation of mGSCs was complex and difficult. What the role A83-01 plays in promoting the proliferation of mGSCs is still unknown. In this study, combined with A83-01 and knockout serum replacement (KSR) medium, we obtained a relatively feeder- and serum-free system for mGSCs culturing in vitro and the optimal concentration of A83-01 was 0.25 μmol L-1. After continuous culturing, the proliferation efficiency of undifferentiated mGSCs and differentiation capacity of mGSC were examined as well. Results showed that, A83-01 dramatically increased the number of mGSCs and AP positive colonies, and the mitosis index according to the BrdU assay. A83-01 could also increase the expression of pluripotent markers including Oct4, Klf4, Nanog and c-Myc, analyzed by real-time quantative PCR. mGSCs cultured in the optimal feeder-and serum-free system combined with A83-01 could form embryoid bodies (EBs), which consisted of three embryonic layers detected by immunofluorescence and RT-PCR. Remarkably, the results demonstrated 0.25 μmol L-1 A83-01 could promote the proliferation of mouse mGSC colonies and maintain their undifferentiated status under feeder- and serum-free systems.

关键词: male germline stem cells (mGSCs) , A83-01 , feeder- and serum-free , mouse

Abstract: A83-01 is a selective inhibitor of the TGF-β type I receptor ALK, which inhibits the TGF-β-induced epithelial-to-mesenchymal transition (EMT) via the inhibition of Smad2 phosphorylation. Previous studies have showed that A83-01 promoted somatic cellular reprogramming significantly. Male germline stem cells (mGSCs), as an alternative resource of pluripotent stem cells derived adult testis, have promising valuable in clinic medicine and regeneration, however, the derivation of mGSCs was complex and difficult. What the role A83-01 plays in promoting the proliferation of mGSCs is still unknown. In this study, combined with A83-01 and knockout serum replacement (KSR) medium, we obtained a relatively feeder- and serum-free system for mGSCs culturing in vitro and the optimal concentration of A83-01 was 0.25 μmol L-1. After continuous culturing, the proliferation efficiency of undifferentiated mGSCs and differentiation capacity of mGSC were examined as well. Results showed that, A83-01 dramatically increased the number of mGSCs and AP positive colonies, and the mitosis index according to the BrdU assay. A83-01 could also increase the expression of pluripotent markers including Oct4, Klf4, Nanog and c-Myc, analyzed by real-time quantative PCR. mGSCs cultured in the optimal feeder-and serum-free system combined with A83-01 could form embryoid bodies (EBs), which consisted of three embryonic layers detected by immunofluorescence and RT-PCR. Remarkably, the results demonstrated 0.25 μmol L-1 A83-01 could promote the proliferation of mouse mGSC colonies and maintain their undifferentiated status under feeder- and serum-free systems.

Key words: male germline stem cells (mGSCs) , A83-01 , feeder- and serum-free , mouse