Normal timing of oligodendrocyte development depends on thyroid hormone receptor alpha 1 (TRα1)

被引:118
作者
Billon, N [1 ]
Jolicoeur, C
Tokumoto, Y
Vennström, B
Raff, M
机构
[1] UCL, MRC, Mol Cell Biol Lab, London WC1E 6BT, England
[2] UCL, Cell Biol Unit, London WC1E 6BT, England
[3] Karolinska Inst, Dept Cell & Mol Biol, S-17177 Stockholm, Sweden
关键词
differentiation; oligodendrocyte; thyroid hormone receptors;
D O I
10.1093/emboj/cdf662
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
The timing of oligodendrocyte development is regulated by thyroid hormone (TH) in vitro and in vivo, but it is still uncertain which TH receptors mediate this regulation. TH acts through nuclear receptors that are encoded by two genes, TRalpha and TRbeta. Here, we provide direct evidence for the involvement of the TRalpha1 receptor isoform in vivo, by showing that the number of oligodendrocytes in the postnatal day 7 (P7) and P14 optic nerve of TRalpha1-/- mice is decreased compared with normal. We demonstrate that TRalpha1 mediates the normal differentiation-promoting effect of TH on oligodendrocyte precursor cells (OPCs): unlike wild-type OPCs, postnatal TRalpha1-/- OPCs fail to stop dividing and differentiate in response to TH in culture. We also show that overexpression of TRalpha1 accelerates oligodendrocyte differentiation in culture, suggesting that the level of TRalpha1 expression is normally limiting for TH-dependent OPC differentiation. Finally, we provide evidence that the inhibitory isoforms of TRalpha are unlikely to play a part in the timing of OPC differentiation.
引用
收藏
页码:6452 / 6460
页数:9
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