Basement membrane collagens and disease mechanisms

被引:71
作者
Gatseva, Anna [1 ]
Sin, Yuan Yan [1 ]
Brezzo, Gaia [1 ,2 ]
Van Agtmael, Tom [1 ]
机构
[1] Univ Glasgow, Inst Cardiovasc & Med Sci, Univ Ave, Glasgow G12 8QQ, Lanark, Scotland
[2] Univ Edinburgh, Sch Med, Ctr Discovery Brain Sci, Edinburgh EH16 4SB, Midlothian, Scotland
来源
EXTRACELLULAR MATRIX | 2019年 / 63卷 / 03期
关键词
DYSTROPHIC EPIDERMOLYSIS-BULLOSA; CONGENITAL MUSCULAR-DYSTROPHY; ANTERIOR SEGMENT DYSGENESIS; LINKED ALPORT SYNDROME; VII COLLAGEN; MOUSE MODEL; STEM-CELLS; MITOCHONDRIAL DYSFUNCTION; EXTRACELLULAR-MATRIX; COL4A1; MUTATIONS;
D O I
10.1042/EBC20180071
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Basement membranes (BMs) are specialised extracellular matrix (ECM) structures and collagens are a key component required for BM function. While collagen IV is the major BM collagen, collagens VI, VII, XV, XVII and XVIII are also present. Mutations in these collagens cause rare multi-systemic diseases but these collagens have also been associated with major common diseases including stroke. Developing treatments for these conditions will require a collective effort to increase our fundamental understanding of the biology of these collagens and the mechanisms by which mutations therein cause disease. Novel insights into pathomolecular disease mechanisms and cellular responses to these mutations has been exploited to develop proof-of-concept treatment strategies in animal models. Combined, these studies have also highlighted the complexity of the disease mechanisms and the need to obtain a more complete understanding of these mechanisms. The identification of pathomolecular mechanisms of collagen mutations shared between different disorders represent an attractive prospect for treatments that may be effective across phenotypically distinct disorders.
引用
收藏
页码:297 / 312
页数:16
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