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皮肤基底膜带疾病——大疱性表皮松解症的范例。

Disorders of the cutaneous basement membrane zone--the paradigm of epidermolysis bullosa.

作者信息

Bruckner-Tuderman Leena, Has Cristina

机构信息

Department of Dermatology, University Medical Center Freiburg, Germany; Freiburg Institute for Advanced Studies, School of Life Sciences - LifeNet, Freiburg, Germany.

Department of Dermatology, University Medical Center Freiburg, Germany.

出版信息

Matrix Biol. 2014 Jan;33:29-34. doi: 10.1016/j.matbio.2013.07.007. Epub 2013 Aug 3.

Abstract

The cutaneous basement membrane zone (BMZ) is a highly specialized functional complex that provides the skin with structural adhesion and resistance to shearing forces. Its regulatory functions include control of epithelial-mesenchymal interactions under physiological and pathological conditions. Mutations in genes encoding components of the BMZ are associated with inherited skin disorders of the epidermolysis bullosa (EB) group, characterized by skin fragility, mechanically induced blisters and erosions of the skin and mucous membranes. Although most disease-associated genes are known, the genetic basis of new EB subtypes linked to mutations in genes for focal adhesion proteins was uncovered only recently. The molecular mechanisms leading to blistering, abnormal wound healing, predisposition to skin cancer, and other complications in EB have been elucidated using animal models and disease proteomics. The rapid progress in understanding the molecular basis of EB has enabled the development of strategies for biologically valid causal therapies.

摘要

皮肤基底膜带(BMZ)是一种高度特化的功能复合体,为皮肤提供结构黏附力并抵抗剪切力。其调节功能包括在生理和病理条件下控制上皮-间充质相互作用。编码BMZ成分的基因突变与大疱性表皮松解症(EB)组的遗传性皮肤病有关,其特征为皮肤脆弱、机械性诱导的水疱以及皮肤和黏膜糜烂。尽管大多数与疾病相关的基因已为人所知,但与黏着斑蛋白基因突变相关的新EB亚型的遗传基础直到最近才被发现。利用动物模型和疾病蛋白质组学已阐明了导致EB中水疱形成、异常伤口愈合、皮肤癌易感性及其他并发症的分子机制。在理解EB分子基础方面的快速进展使得开发具有生物学有效性的因果疗法策略成为可能。

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