Glutathione peroxidase-1 is required for self-renewal of murine embryonic stem cells

被引:8
作者
Wang, Qian-Yi [1 ]
Liu, Zhao-Shan [1 ]
Wang, Jie [1 ]
Wang, Hong-Xia [1 ]
Li, Ang [1 ]
Yang, Yang [1 ]
Wang, Xin-Zheng [1 ]
Zhao, Yong-Qiang [1 ]
Han, Qiu-Ying [1 ]
Cai, Hong [1 ]
Liang, Bing [1 ]
Song, Nan [1 ]
Li, Wei-Hua [1 ]
Li, Tao [1 ]
机构
[1] Natl Ctr Biomed Anal, Inst Basic Med Sci, State Key Lab Proteom, Beijing 100850, Peoples R China
关键词
Embryonic stem cells; Glutathione peroxidase-1; Self-renewal; Differentiation; OXIDATIVE STRESS; ES CELLS; OXYGEN; DIFFERENTIATION; PLURIPOTENCY; MAINTENANCE; MECHANISMS; CULTURE; NICHE; LIFE;
D O I
10.1016/j.bbrc.2014.04.139
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:454 / 460
页数:7
相关论文
共 35 条
[1]   Relative contributions of heart mitochondria glutathione peroxidase and catalase to H2O2 detoxification in in vivo conditions [J].
Antunes, F ;
Han, D ;
Cadenas, E .
FREE RADICAL BIOLOGY AND MEDICINE, 2002, 33 (09) :1260-1267
[2]   Multipotent cell lineages in early mouse development depend on SOX2 function [J].
Avilion, AA ;
Nicolis, SK ;
Pevny, LH ;
Perez, L ;
Vivian, N ;
Lovell-Badge, R .
GENES & DEVELOPMENT, 2003, 17 (01) :126-140
[3]   Oxygen accelerates the accumulation of mutations during the senescence and immortalization of murine cells in culture [J].
Busuttil, RA ;
Rubio, M ;
Dollé, MET ;
Campisi, J ;
Vijg, J .
AGING CELL, 2003, 2 (06) :287-294
[4]   Oxidative stress impairs endothelial progenitor cell function [J].
Case, Jamie ;
Ingram, David A. ;
Haneline, Laura S. .
ANTIOXIDANTS & REDOX SIGNALING, 2008, 10 (11) :1895-1907
[5]  
CHAUDIERE J, 1984, J BIOL CHEM, V259, P1043
[6]   Dynamic changes in mitochondrial biogenesis and antioxidant enzymes during the spontaneous differentiation of human embryonic stem cells [J].
Cho, Young Min ;
Kwon, Sujin ;
Pak, Youngmi Kim ;
Seol, Hye Won ;
Choi, Young Min ;
Park, Do Joon ;
Park, Kyong Soo ;
Lee, Hong Kyu .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2006, 348 (04) :1472-1478
[7]   GLUTATHIONE PEROXIDASE - PRIMARY AGENT FOR ELIMINATION OF HYDROGEN PEROXIDE IN ERYTHROCYTES [J].
COHEN, G ;
HOCHSTEIN, P .
BIOCHEMISTRY, 1963, 2 (06) :1420-&
[8]   Ronin is essential for embryogenesis and the pluripotency of mouse embryonic stem cells [J].
Dejosez, Marion ;
Krumenacker, Joshua S. ;
Zitur, Laura Jo ;
Passeri, Marco ;
Chu, Li-Fang ;
Zhou Songyang ;
Thomson, James A. ;
Zwaka, Thomas P. .
CELL, 2008, 133 (07) :1162-1174
[9]   A p38 inhibitor allows to dissociate differentiation and apoptotic processes triggered upon LIF withdrawal in mouse embryonic stem cells [J].
Duval, D ;
Malaisé, M ;
Reinhardt, B ;
Kedinger, C ;
Boeuf, H .
CELL DEATH AND DIFFERENTIATION, 2004, 11 (03) :331-341
[10]   Discovering pluripotency: 30 years of mouse embryonic stem cells [J].
Evans, Martin .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2011, 12 (10) :680-686