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Two molecularly distinct intracellular pathways to oligodendrocyte differentiation: role of a p53 family protein

机译:少突胶质细胞分化的两种分子内不同的细胞内途径:p53家族蛋白的作用

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摘要

Both thyroid hormone (TH) and retinoic acid (RA) induce purified rat oligodendrocyte precursor cells in culture to stop division and differentiate. We show that these responses are blocked by the expression of a dominant-negative form of p53. Moreover, both TH and RA cause a transient, immediate early increase in the same 8 out of 13 mRNAs encoding intracellular cell cycle regulators and gene regulatory proteins, but only if protein synthesis is inhibited. Platelet-derived growth factor (PDGF) withdrawal also induces these cells to differentiate, but we show that the intracellular mechanisms involved are different from those involved in the hormone responses: the changes in cell cycle regulators differ, and the differentiation induced by PDGF withdrawal (or that which occurs spontaneously in the presence of PDGF) is not blocked by the dominant-negative p53. These results suggest that TH and RA activate the same intracellular pathway leading to oligodendrocyte differentiation, and that this pathway depends on a p53 family protein. Differentiation that occurs independently of TH and RA apparently involves a different pathway. It is likely that both pathways operate in vivo.
机译:甲状腺激素(TH)和视黄酸(RA)均可诱导培养物中纯化的大鼠少突胶质前体细胞停止分裂和分化。我们显示这些反应被p53显性负型的表达所阻断。而且,TH和RA都会导致编码细胞内细胞周期调节剂和基因调节蛋白的13种mRNA中的同一8种瞬时瞬时增加,但前提是蛋白合成受到抑制。血小板衍生的生长因子(PDGF)撤离也会诱导这些细胞分化,但我们证明所涉及的细胞内机制与激素反应所涉及的机制不同:细胞周期调节剂的变化各不相同,PDGF撤离诱导的分化(或在PDGF存在下自然发生的现象)不会被显性阴性p53阻断。这些结果表明TH和RA激活相同的细胞内途径,导致少突胶质细胞分化,并且该途径取决于p53家族蛋白。独立于TH和RA发生的分化显然涉及不同的途径。这两种途径都可能在体内起作用。

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