Roles for p53 and p73 during oligodendrocyte development

被引:91
作者
Billon, N
Terrinoni, A
Jolicoeur, C
McCarthy, A
Richardson, WD
Melino, G
Raff, M
机构
[1] UCL, MRC Lab Mol Cell Biol, London WC1E 6BT, England
[2] UCL, Cell Biol Unit, London WC1E 6BT, England
[3] Univ Roma Tor Vergata, Biochem Lab, I-00133 Rome, Italy
[4] London Inst Canc Res, Breakthrough Breast Canc Ctr, London SW3 6JB, England
[5] UCL, Wolfson Inst Biomed Res, London WC1E 6BT, England
[6] Univ Leicester, MRC Toxicol Unit, Leicester LE1 9HN, Leics, England
来源
DEVELOPMENT | 2004年 / 131卷 / 06期
关键词
differentiation; oligodendrocyte; p53; p63; p73; rat;
D O I
10.1242/dev.01035
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Oligodendrocytes make myelin in the vertebrate central nervous system (CNS). They develop from oligodendrocyte precursor cells (OPCs), most of which divide a limited number of times before they stop and differentiate. OPCs can be purified from the developing rat optic nerve and stimulated to proliferate in serum-free culture by PDGE They can be induced to differentiate in vitro by either thyroid hormone (TH) or PDGF withdrawal. It was shown previously that a dominant-negative form of p53 could inhibit OPC differentiation induced by TH but not by PDGF withdrawal, suggesting that the p53 family of proteins might play a part in TH-induced differentiation. As the dominant-negative p53 used inhibited all three known p53 family members - p53, p63 and p73 - it was uncertain which family members are important for this process. Here, we provide evidence that both p53 and p73, but not p63, are involved in TH-induced OPC differentiation and that p73 also plays a crucial part in PDGF-withdrawal-induced differentiation. This is the first evidence for a role of p73 in the differentiation of a normal mammalian cell.
引用
收藏
页码:1211 / 1220
页数:10
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