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 PDGF. 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.
Roles for p53 and p73 during oligodendrocyte development
Present address: Department of Biological Sciences, Howard Hughes Medical Institute, 371 Serra Mall, Stanford University, CA 94305-5020, USA
Nathalie Billon, Alessandro Terrinoni, Christine Jolicoeur, Afshan McCarthy, William D. Richardson, Gerry Melino, Martin Raff; Roles for p53 and p73 during oligodendrocyte development. Development 15 March 2004; 131 (6): 1211–1220. doi: https://doi.org/10.1242/dev.01035
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