Glucocorticoid receptor enhances involucrin expression of keratinocyte in a ligand-independent manner

In this study, we investigated the role of glucocorticoid receptor (GR) in epidermal keratinocytes. In adult normal human skin, GR was highly expressed in the upper layers of the epidermis. Consistent with normal skin, GR expression was increased after calcium treatment of HaCaT keratinocytes cultur...

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Veröffentlicht in:Molecular and cellular biochemistry 2014-05, Vol.390 (1-2), p.289-295
Hauptverfasser: Yoon, Hyun Kyung, Li, Zheng Jun, Choi, Dae-Kyoung, Sohn, Kyung-Cheol, Lim, Eun-Hwa, Lee, Young Ho, Kim, Sooil, Im, Myung, Lee, Young, Seo, Young-Joon, Lee, Jeung-Hoon, Kim, Chang Deok
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Sprache:eng
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Zusammenfassung:In this study, we investigated the role of glucocorticoid receptor (GR) in epidermal keratinocytes. In adult normal human skin, GR was highly expressed in the upper layers of the epidermis. Consistent with normal skin, GR expression was increased after calcium treatment of HaCaT keratinocytes cultured in vitro, suggesting that GR is involved in keratinocyte differentiation process. Overexpression of GR using an adenovirus showed that expression of involucrin, an early differentiation marker of keratinocytes, was markedly increased due to GR overexpression. However, treatment with dexamethasone, a GR agonist, did not increase involucrin expression. Overexpression of GR led to phosphorylation of c-Jun N-terminal kinase (JNK) and extracellular signal-regulated kinases (ERK) in the absence of glucocorticoid, suggesting that the GR effect on involucrin expression is related to activation of intracellular signaling cascades. This idea was supported by the fact that GR-mediated involucrin induction was abolished after treatment with JNK and ERK inhibitors. In addition, GR mutants lacking the ligand-binding domain increased involucrin expression concomitantly with increase of ERK phosphorylation. Together, these results suggest that GR modulates involucrin expression of keratinocytes by regulating the intracellular signaling network in a ligand-independent manner.
ISSN:0300-8177
1573-4919
DOI:10.1007/s11010-014-1985-7