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体内长期暴露于阳光下的皮肤中角质形成细胞β1整合素表达降低。

Decreased expression of keratinocyte beta1 integrins in chronically sun-exposed skin in vivo.

作者信息

Bosset S, Bonnet-Duquennoy M, Barré P, Chalon A, Lazou K, Kurfurst R, Bonté F, Schnébert S, Disant F, Le Varlet B, Nicolas J F

机构信息

INSERM U503, Université Claude Bernard et Hospices Civils de Lyon, 21 Av. Tony Garnier, 69007 Lyon, France.

出版信息

Br J Dermatol. 2003 Apr;148(4):770-8. doi: 10.1046/j.1365-2133.2003.05159.x.

Abstract

BACKGROUND

Chronic exposure to ultraviolet (UV) radiation induces changes in the skin structure which are mostly found in the superficial dermis and at the dermal-epidermal junction. Keratinocytes and fibroblasts contribute both to the synthesis and to the degradation of the molecules important for the integrity of this skin site. While several studies have reported on alterations of dermal components and of the functions of fibroblasts in vivo and in vitro after UV exposure, recent data suggested that keratinocytes could be the main skin cell type involved in the photoageing process.

OBJECTIVES

In this study, we analysed the expression of two keratinocyte molecules namely, beta1 integrin (a proliferation marker) and involucrin (a differentiation marker) in sun-exposed and sun-protected facial skin of 16 healthy patients undergoing facial lifting.

METHODS

Methods included histology, immunohistochemistry and quantitative reverse transcriptase-polymerase chain reaction analysis.

RESULTS

Sun-exposed skin displayed the characteristic morphological and molecular features of dermal photoageing, compared with sun-protected skin, including dermal elastosis, diminished fibrillin and type VII collagen expression. Analysis of the epidermis in sun-exposed vs. sun-protected skin showed no histological differences, but dramatic changes in the expression of beta1 integrin and involucrin. In sun-exposed skin, expression of beta1 integrin protein by epidermal basal cells was reduced, paralleling a downregulation of beta1 integrin mRNA, whereas involucrin protein expression was greatly enhanced in the superficial epidermal cell layers. Interestingly, the ratio between involucrin and beta1 integrin protein expression was consistently increased in sun-exposed skin sites.

CONCLUSIONS

Collectively these results demonstrate that epidermal homeostasis is impaired by chronic UV exposure, and define beta1 integrin expression as a molecular marker of the epidermal photoageing process.

摘要

背景

长期暴露于紫外线(UV)会导致皮肤结构发生变化,这些变化主要出现在真皮浅层和真皮-表皮交界处。角质形成细胞和成纤维细胞都参与了对该皮肤部位完整性至关重要的分子的合成和降解。虽然有几项研究报道了紫外线照射后体内和体外真皮成分及成纤维细胞功能的改变,但最近的数据表明角质形成细胞可能是光老化过程中主要涉及的皮肤细胞类型。

目的

在本研究中,我们分析了16名接受面部提升的健康患者暴露于阳光和受阳光保护的面部皮肤中两种角质形成细胞分子,即β1整合素(一种增殖标志物)和兜甲蛋白(一种分化标志物)的表达情况。

方法

方法包括组织学、免疫组织化学和定量逆转录聚合酶链反应分析。

结果

与受阳光保护的皮肤相比,暴露于阳光的皮肤表现出真皮光老化的特征性形态和分子特征,包括真皮弹性组织变性、原纤蛋白和VII型胶原蛋白表达减少。对暴露于阳光与受阳光保护的皮肤的表皮分析显示,组织学上没有差异,但β1整合素和兜甲蛋白的表达有显著变化。在暴露于阳光的皮肤中,表皮基底细胞中β1整合素蛋白的表达降低,同时β1整合素mRNA下调,而兜甲蛋白在表皮浅层细胞层中的蛋白表达大大增强。有趣的是,在暴露于阳光的皮肤部位,兜甲蛋白与β1整合素蛋白表达的比值持续增加。

结论

这些结果共同表明,长期紫外线暴露会损害表皮稳态,并将β1整合素表达定义为表皮光老化过程的分子标志物。

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