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锌、铜和锰对角质形成细胞伤口愈合整合素的体外调节作用

In vitro modulation of keratinocyte wound healing integrins by zinc, copper and manganese.

作者信息

Tenaud I, Sainte-Marie I, Jumbou O, Litoux P, Dréno B

机构信息

Laboratory of Immuno-Dermatology, CHU Hôtel-Dieu, Place A. Ricordeau, 44035 Nantes Cedex 01, France.

出版信息

Br J Dermatol. 1999 Jan;140(1):26-34. doi: 10.1046/j.1365-2133.1999.02603.x.

DOI:10.1046/j.1365-2133.1999.02603.x
PMID:10215764
Abstract

Although the trace elements zinc, copper and manganese are used in vivo for their healing properties, their mechanism of action is still only partially known. Some integrins expressed by basal layer keratinocytes play an essential part in healing, notably alpha2beta1, alpha3beta1, alpha6beta4 and alphaVbeta5, whose expression and distribution in epidermis are modified during the re-epithelialization phase. This study demonstrates how the expression of these integrins are modulated in vitro by trace elements. Integrin expression was studied in proliferating keratinocytes in monolayer cultures and in reconstituted skin that included a differentiation state. After 48 h incubation with zinc gluconate (0.9, 1.8 and 3.6 microg/mL), copper gluconate (1, 2 and 4 microg/mL), manganese gluconate (0.5, 1 and 2 microg/mL) and control medium, integrin expression was evaluated by FACScan and immunohistochemistry. Induction of alpha2, alpha3, alphaV and alpha6 was produced by zinc gluconate 1.8 microg/mL in monolayers, of alpha2, alpha6 and beta1 by copper gluconate 2 and 4 microg/mL and of all the integrins studied except alpha3 by manganese gluconate 1 microg/mL. Thus, alpha6 expression was induced by all three trace elements. The inductive effect of zinc was particularly notable on integrins affecting cellular mobility in the proliferation phase of wound healing (alpha3, alpha6, alphaV) and that of copper on integrins expressed by suprabasally differentiated keratinocytes during the final healing phase (alpha2, beta1 and alpha6), while manganese had a mixed effect.

摘要

尽管微量元素锌、铜和锰在体内因其愈合特性而被利用,但其作用机制仍仅部分为人所知。基底层角质形成细胞表达的一些整合素在愈合过程中起重要作用,特别是α2β1、α3β1、α6β4和αVβ5,它们在表皮中的表达和分布在重新上皮化阶段会发生改变。本研究证明了这些整合素的表达在体外如何受到微量元素的调节。在单层培养的增殖角质形成细胞和具有分化状态的重组皮肤中研究了整合素的表达。在用葡萄糖酸锌(0.9、1.8和3.6微克/毫升)、葡萄糖酸铜(1、2和4微克/毫升)、葡萄糖酸锰(0.5、1和2微克/毫升)和对照培养基孵育48小时后,通过流式细胞仪和免疫组织化学评估整合素的表达。1.8微克/毫升的葡萄糖酸锌在单层培养中诱导了α2、α3、αV和α6的表达,2和4微克/毫升的葡萄糖酸铜诱导了α2、α6和β1的表达,1微克/毫升的葡萄糖酸锰诱导了除α3外所有研究整合素的表达。因此,所有三种微量元素都诱导了α6的表达。锌对影响伤口愈合增殖期细胞迁移的整合素(α3、α6、αV)的诱导作用尤为显著,铜对最终愈合期基底上层分化角质形成细胞表达的整合素(α2、β1和α6)的诱导作用显著,而锰则具有混合作用。

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