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皮肤基底膜:表皮完整性的基础——连接分子巢蛋白和层粘连蛋白的 BM 功能和多种作用。

Skin basement membrane: the foundation of epidermal integrity--BM functions and diverse roles of bridging molecules nidogen and perlecan.

机构信息

Department of Dermatology, University of Cologne, Kerpener Strasse 62, 50937 Cologne, Germany.

出版信息

Biomed Res Int. 2013;2013:179784. doi: 10.1155/2013/179784. Epub 2013 Mar 21.

DOI:10.1155/2013/179784
PMID:23586018
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3618921/
Abstract

The epidermis functions in skin as first defense line or barrier against environmental impacts, resting on extracellular matrix (ECM) of the dermis underneath. Both compartments are connected by the basement membrane (BM), composed of a set of distinct glycoproteins and proteoglycans. Herein we are reviewing molecular aspects of BM structure, composition, and function regarding not only (i) the dermoepidermal interface but also (ii) the resident microvasculature, primarily focusing on the per se nonscaffold forming components perlecan and nidogen-1 and nidogen-2. Depletion or functional deficiencies of any BM component are lethal at some stage of development or around birth, though BM defects vary between organs and tissues. Lethality problems were overcome by developmental stage- and skin-specific gene targeting or by cell grafting and organotypic (3D) cocultures of normal or defective cells, which allows recapitulating BM formation de novo. Thus, evidence is accumulating that BM assembly and turnover rely on mechanical properties and composition of the adjacent ECM and the dynamics of molecular assembly, including further "minor" local components, nidogens largely functioning as catalysts or molecular adaptors and perlecan as bridging stabilizer. Collectively, orchestration of BM assembly, remodeling, and the role of individual players herein are determined by the developmental, tissue-specific, or functional context.

摘要

表皮在皮肤中作为第一道防线或屏障,抵御环境影响,位于下方真皮的细胞外基质 (ECM) 上。这两个隔室通过基底膜 (BM) 连接,基底膜由一组独特的糖蛋白和蛋白聚糖组成。在此,我们回顾了 BM 结构、组成和功能的分子方面,不仅涉及 (i) 表皮真皮界面,还涉及 (ii) 常驻微血管,主要关注本身不形成支架的成分——聚糖蛋白和巢蛋白-1 和巢蛋白-2。任何 BM 成分的耗竭或功能缺陷在发育的某个阶段或出生前后都是致命的,尽管 BM 缺陷在不同的器官和组织之间有所不同。通过发育阶段和皮肤特异性基因靶向或通过正常或有缺陷细胞的细胞移植和器官样(3D)共培养,可以克服致死性问题,从而允许从头开始重新形成 BM。因此,越来越多的证据表明,BM 的组装和周转依赖于相邻 ECM 的机械特性和组成以及分子组装的动力学,包括进一步的“次要”局部成分,巢蛋白主要作为催化剂或分子接头,而聚糖蛋白作为桥接稳定剂。总的来说,BM 组装、重塑以及其中各个参与者的作用取决于发育、组织特异性或功能背景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7275/3618921/a22402f3353e/BMRI2013-179784.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7275/3618921/e584848adff9/BMRI2013-179784.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7275/3618921/a22402f3353e/BMRI2013-179784.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7275/3618921/e584848adff9/BMRI2013-179784.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7275/3618921/a22402f3353e/BMRI2013-179784.002.jpg

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