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局部外用维甲酸治疗的皮肤中表皮α2β1和α3β1整合素的基底层上表达

Suprabasal expression of epidermal alpha 2 beta 1 and alpha 3 beta 1 integrins in skin treated with topical retinoic acid.

作者信息

Häkkinen L, Westermarck J, Johansson N, Aho H, Peltonen J, Heino J, Kähäri V M

机构信息

Department of Periodontology, Medical Biochemistry and Pathology, University of Turku, Finland.

出版信息

Br J Dermatol. 1998 Jan;138(1):29-36. doi: 10.1046/j.1365-2133.1998.02023.x.

Abstract

In normal adult human skin, expression of epidermal integrins is confined to keratinocytes in the basal layer. However, suprabasal expression of alpha 2, alpha 3 and beta 1 integrin subunits is noted in hyperproliferative epidermis in wound repair and psoriasis. In this study, we examined the effect of topical all-trans-retinoic acid (RA), known to induce epidermal hyperplasia, on expression of integrins in human epidermis. Immunostaining of vehicle-treated skin revealed expression of alpha 2, alpha 3 and beta 1, as well as alpha 6 and beta 4 integrin subunits entirely on basal keratinocytes. Topical application of RA (0.1%) for 2 weeks resulted in marked suprabasal expression of alpha 2, alpha 3 and beta 1 integrin subunits, whereas alpha 6 and beta 4 staining remained on basal keratinocytes. Staining for putative ligands of alpha 2 beta 1 and alpha 3 beta 1 integrins, i.e. type IV collagen, laminin-5 and fibronectin, was not detected in the epidermal layer in RA- or vehicle-treated skin. Treatment of HaCaT keratinocytes in culture with RA (1 mumol/L) enhanced alpha 2 and beta 1 mRNA abundance. Furthermore, RA slightly up-regulated the expression of alpha 2, alpha 3 and beta 1 integrin subunits on primary epidermal keratinocytes and HaCaT cells in culture with no effect on cell proliferation. These results provide evidence that RA-elicited epidermal hyperplasia is associated with aberrant suprabasal expression of alpha 2 beta 1 and alpha 3 beta 1 integrins, and that this also involves direct stimulation of keratinocyte integrin expression by RA.

摘要

在正常成人皮肤中,表皮整合素的表达局限于基底层的角质形成细胞。然而,在伤口修复和银屑病的增生性表皮中,可观察到α2、α3和β1整合素亚基的基底层以上表达。在本研究中,我们检测了已知可诱导表皮增生的外用全反式维甲酸(RA)对人表皮整合素表达的影响。用赋形剂处理的皮肤免疫染色显示,α2、α3和β1以及α6和β4整合素亚基完全表达于基底角质形成细胞。外用RA(0.1%)2周导致α2、α3和β1整合素亚基显著的基底层以上表达,而α6和β4染色仍局限于基底角质形成细胞。在RA或赋形剂处理的皮肤表皮层中未检测到α2β1和α3β1整合素假定配体(即IV型胶原、层粘连蛋白-5和纤连蛋白)的染色。用RA(1μmol/L)处理培养的HaCaT角质形成细胞可增加α2和β1 mRNA丰度。此外,RA略微上调了原代表皮角质形成细胞和培养的HaCaT细胞中α2、α3和β1整合素亚基的表达,对细胞增殖无影响。这些结果证明,RA诱导的表皮增生与α2β1和α3β1整合素异常的基底层以上表达有关,并且这也涉及RA对角质形成细胞整合素表达的直接刺激。

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