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O-2A祖细胞系CG-4分化过程中Krox蛋白的表达。

Expression of Krox proteins during differentiation of the O-2A progenitor cell line CG-4.

作者信息

Sock E, Leger H, Kuhlbrodt K, Schreiber J, Enderich J, Richter-Landsberg C, Wegner M

机构信息

Zentrum für Molekulare Neurobiologie, Universität Hamburg, Germany.

出版信息

J Neurochem. 1997 May;68(5):1911-9. doi: 10.1046/j.1471-4159.1997.68051911.x.

Abstract

Krox proteins are important regulators of development and terminal differentiation. Using the rat glial progenitor cell line CG-4 as a model system for oligodendrocyte differentiation, we show that on the RNA level Krox-24 is the predominant member of the Krox family in these cells. Similar results were also obtained on the protein level as the major Krox protein from CG-4 cell extracts reacted specifically with an antibody against Krox-24. Whereas Krox-24 RNA and protein were abundant in undifferentiated CG-4 cells, a dramatic decrease in expression was detected after a 3-5-day period of differentiation during which we observed a reciprocal increase in the levels of myelin basic protein expression. Importantly, regulation of Krox-24 expression was very similar in CG-4 cells and primary oligodendrocyte cultures. When expression of Krox-24 in differentiating CG-4 cells was followed on a closer time scale, we observed a sharp and transient increase in Krox-24 RNA, protein, and DNA binding activity immediately after the onset of differentiation followed by an equally rapid decrease. This expression pattern implicates Krox-24 both in maintenance of the undifferentiated state and in the immediate early phase of differentiation of CG-4 cells and possibly oligodendrocytes.

摘要

Krox蛋白是发育和终末分化的重要调节因子。我们以大鼠神经胶质祖细胞系CG-4作为少突胶质细胞分化的模型系统,发现在RNA水平上,Krox-24是这些细胞中Krox家族的主要成员。在蛋白质水平上也得到了类似结果,因为来自CG-4细胞提取物的主要Krox蛋白与抗Krox-24抗体发生特异性反应。未分化的CG-4细胞中Krox-24的RNA和蛋白质含量丰富,但在分化3-5天后,其表达显著下降,在此期间我们观察到髓鞘碱性蛋白表达水平相应增加。重要的是,CG-4细胞和原代少突胶质细胞培养物中Krox-24的表达调控非常相似。当在更短的时间尺度上追踪分化的CG-4细胞中Krox-24的表达时,我们观察到分化开始后,Krox-24的RNA、蛋白质和DNA结合活性立即急剧短暂增加,随后同样迅速下降。这种表达模式表明Krox-24既参与维持CG-4细胞以及可能还有少突胶质细胞的未分化状态,也参与其分化的早期阶段。

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