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小Rho GTP酶Rac1表达的抑制可诱导人成年角质形成细胞分化,而对其增殖无影响。

The inhibition of the expression of the small Rho GTPase Rac1 induces differentiation with no effect on cell proliferation in growing human adult keratinocytes.

作者信息

Nikolova Ekaterina, Mitev Vanio, Minner Frédéric, Deroanne Christophe F, Poumay Yves

机构信息

Cell and Tissue Laboratory, URPHYM, University of Namur (FUNDP), B-5000 Namur, Belgium.

出版信息

J Cell Biochem. 2008 Feb 15;103(3):857-64. doi: 10.1002/jcb.21455.

Abstract

Rac1 is a Rho subfamily small GTPase which is highly expressed in epidermal keratinocytes. In mice the significance of Rac1 for the maintenance of the epidermis has been controversial. In keratinocytes from human origin, the role of Rac1 in the control of growth/differentiation is still obscure. In this study we used RNA interference to induce specific inhibition of Rac1 expression in cultured human keratinocytes and analyzed the consequences on proliferation and differentiation. We found that the autocrine proliferation of keratinocytes is unaltered by Rac1 silencing. However, the suppression of Rac1 induced premature differentiation as revealed by the expression of markers (keratin 10, involucrin), but the involved mechanism is independent of the activity of p38 mitogen-activated protein kinase. Rather, we found that the effects of Rac1 silencing on keratinocytes differentiation are concomitant with negative regulation of the Ser62/Thr58 phosphorylation on the transcription factor c-myc, a mechanism known to control post-translational stability of the c-myc protein. Thus, in growing human keratinocytes, Rac1 could impede the expression of premature differentiation markers, probably by exerting positive control on c-myc activity and its binding to specific promoters.

摘要

Rac1是一种Rho亚家族小GTP酶,在表皮角质形成细胞中高度表达。在小鼠中,Rac1对维持表皮的重要性一直存在争议。在源自人类的角质形成细胞中,Rac1在控制生长/分化中的作用仍不清楚。在本研究中,我们使用RNA干扰在培养的人角质形成细胞中诱导Rac1表达的特异性抑制,并分析其对增殖和分化的影响。我们发现,Rac1沉默不会改变角质形成细胞的自分泌增殖。然而,Rac1的抑制诱导了过早分化,这通过标志物(角蛋白10、内披蛋白)的表达得以揭示,但所涉及的机制独立于p38丝裂原活化蛋白激酶的活性。相反,我们发现Rac1沉默对角质形成细胞分化的影响与转录因子c-myc上Ser62/Thr58磷酸化的负调控同时发生,这是一种已知控制c-myc蛋白翻译后稳定性的机制。因此,在生长的人角质形成细胞中,Rac1可能通过对c-myc活性及其与特定启动子的结合施加正向控制,从而阻碍过早分化标志物的表达。

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