| Literature DB >> 24802396 |
Qian-Yi Wang1, Zhao-Shan Liu1, Jie Wang1, Hong-Xia Wang1, Ang Li1, Yang Yang1, Xin-Zheng Wang1, Yong-Qiang Zhao1, Qiu-Ying Han1, Hong Cai1, Bing Liang1, Nan Song1, Wei-Hua Li1, Tao Li2.
Abstract
Embryonic stem (ES) cells are pluripotent cells that are capable of giving rise to any type of cells in the body and possess unlimited self-renewal potential. However, the exact regulatory mechanisms that govern the self-renewal ability of ES cells remain elusive. To understand the immediate early events during ES cell differentiation, we performed a proteomics study and analyzed the proteomic difference in murine ES cells before and after a 6-h spontaneous differentiation. We found that the expression level of glutathione peroxidase-1 (GPx-1), an antioxidant enzyme, is dramatically decreased upon the differentiation. Both knockdown of GPx-1 expression with shRNA and inhibiting GPx-1 activity by inhibitor led to the differentiation of ES cells. Furthermore, we showed that during early differentiation, the quick degradation of GPx-1 was mediated by proteasome. Thus, our data indicated that GPx-1 is a key regulator of self-renewal of murine embryonic stem cells.Entities:
Keywords: Differentiation; Embryonic stem cells; Glutathione peroxidase-1; Self-renewal
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Year: 2014 PMID: 24802396 DOI: 10.1016/j.bbrc.2014.04.139
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575