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The inhibition of the expression of the small Rho GTPase Rac1 induces differentiation with no effect on cell proliferation in growing human adult keratinocytes
Author(s) -
Nikolova Ekaterina,
Mitev Vanio,
Minner Frédéric,
Deroanne Christophe F.,
Poumay Yves
Publication year - 2007
Publication title -
journal of cellular biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.028
H-Index - 165
eISSN - 1097-4644
pISSN - 0730-2312
DOI - 10.1002/jcb.21455
Subject(s) - rac1 , involucrin , biology , microbiology and biotechnology , gene silencing , cellular differentiation , small gtpase , keratinocyte , rna interference , signal transduction , cell culture , rna , biochemistry , genetics , gene
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. J. Cell. Biochem. 103: 857–864, 2008. © 2007 Wiley‐Liss, Inc.