Kahlina Kornelija, Goren Itamar, Pfeilschifter Josef, Frank Stefan
Pharmazentrum Frankfurt, Klinikum der Johann Wolfgang Goethe-Universität, Theodor-Stern-Kai 7, D-60590 Frankfurt am Main, Germany.
J Biol Chem. 2004 Oct 22;279(43):44872-82. doi: 10.1074/jbc.M402467200. Epub 2004 Aug 10.
Nitric oxide (NO) represents a short lived mediator that pivotally drives keratinocyte movements during cutaneous wound healing. In this study, we have identified p68 DEAD box RNA helicase (p68) from an NO-induced differential keratinocyte cDNA library. Subsequently, we have analyzed regulation of p68 by wound-associated mediators in human and murine keratinocytes. NO, serum, growth factors, and pro-inflammatory cytokines were potent inducers of p68 expression in the cells. p68 was constitutively expressed in the epithelial compartment of murine skin. Upon injury, we found a transient down-regulation of overall p68 protein in wound tissue. However, p68 did not completely disappear during early wound repair, as we found an expression of p68 protein in isolated wound margin tissue 24 h after wounding. Moreover, immunohistochemistry and cell fractionation analysis revealed a restricted localization of p68 in keratinocyte nuclei of the developing epithelium. Accordingly, cultured keratinocytes also showed a nuclear localization of the helicase. Moreover, confocal microscopy revealed a strong localization of p68 protein within the nucleoli of the cells. Functional analyses demonstrated that p68 strongly participated in keratinocyte proliferation and gene expression. Keratinocytes that constitutively overexpressed p68 protein were characterized by a marked increase in serum-induced proliferation and vascular endothelial growth factor expression, whereas down-regulation of endogenous p68 using small interfering RNA markedly attenuated serum-induced proliferation and vascular endothelial growth factor expression. Altogether, our results suggest a tightly controlled expression and nucleolar localization of p68 in keratinocytes in vitro and during skin repair in vivo that functionally contributes to keratinocyte proliferation and gene expression.
一氧化氮(NO)是一种半衰期较短的介质,在皮肤伤口愈合过程中对角质形成细胞的移动起着关键驱动作用。在本研究中,我们从一个NO诱导的角质形成细胞差异cDNA文库中鉴定出了p68 DEAD盒RNA解旋酶(p68)。随后,我们分析了人及小鼠角质形成细胞中伤口相关介质对p68的调控。NO、血清、生长因子和促炎细胞因子是细胞中p68表达的有效诱导剂。p68在小鼠皮肤的上皮区域组成性表达。受伤后,我们发现伤口组织中p68蛋白整体出现短暂下调。然而,在伤口早期修复过程中p68并未完全消失,因为我们发现受伤24小时后分离的伤口边缘组织中有p68蛋白表达。此外,免疫组织化学和细胞分级分析显示p68在发育中上皮的角质形成细胞核内定位受限。相应地,培养的角质形成细胞也显示出解旋酶的核定位。此外,共聚焦显微镜显示p68蛋白在细胞的核仁内有强烈定位。功能分析表明p68强烈参与角质形成细胞的增殖和基因表达。持续过表达p68蛋白的角质形成细胞的特征是血清诱导的增殖和血管内皮生长因子表达显著增加,而使用小干扰RNA下调内源性p68则显著减弱血清诱导的增殖和血管内皮生长因子表达。总之,我们的结果表明,p68在体外角质形成细胞和体内皮肤修复过程中的表达和核仁定位受到严格控制,在功能上有助于角质形成细胞的增殖和基因表达。