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次卤酸在基底膜稳态中的作用。

Role of Hypohalous Acids in Basement Membrane Homeostasis.

作者信息

Colon Selene, Page-McCaw Patrick, Bhave Gautam

机构信息

1 Division of Nephrology, Department of Medicine, Vanderbilt University Medical Center , Nashville, Tennessee.

2 Department of Biological Sciences, Tennessee State University , Nashville, Tennessee.

出版信息

Antioxid Redox Signal. 2017 Oct 20;27(12):839-854. doi: 10.1089/ars.2017.7245. Epub 2017 Jul 31.

Abstract

SIGNIFICANCE

Basement membranes (BMs) are sheet-like structures of specialized extracellular matrix that underlie nearly all tissue cell layers including epithelial, endothelial, and muscle cells. BMs not only provide structural support but are also critical for the development, maintenance, and repair of organs. Animal heme peroxidases generate highly reactive hypohalous acids extracellularly and, therefore, target BMs for oxidative modification. Given the importance of BMs in tissue structure and function, hypohalous acid-mediated oxidative modifications of BM proteins represent a key mechanism in normal development and pathogenesis of disease. Recent Advances: Peroxidasin (PXDN), a BM-associated animal heme peroxidase, generates hypobromous acid (HOBr) to form sulfilimine cross-links within the collagen IV network of BM. These cross-links stabilize BM and are critical for animal tissue development. These findings highlight a paradoxical anabolic role for HOBr, which typically damages protein structure leading to dysfunction.

CRITICAL ISSUES

The molecular mechanism whereby PXDN uses HOBr as a reactive intermediate to cross-link collagen IV, yet avoid collateral damage to nearby BM proteins, remains unclear.

FUTURE DIRECTIONS

The exact identification and functional impact of specific hypohalous acid-mediated modifications of BM proteins need to be addressed to connect these modifications to tissue development and pathogenesis of disease. As seen with the sulfilimine cross-link of collagen IV, hypohalous acid oxidative events may be beneficial in select situations rather than uniformly deleterious. Antioxid. Redox Signal. 27, 839-854.

摘要

意义

基底膜(BMs)是特殊细胞外基质的片状结构,几乎位于所有组织细胞层之下,包括上皮细胞、内皮细胞和肌肉细胞。基底膜不仅提供结构支持,对器官的发育、维持和修复也至关重要。动物血红素过氧化物酶在细胞外产生高反应性的次卤酸,因此将基底膜作为氧化修饰的靶点。鉴于基底膜在组织结构和功能中的重要性,次卤酸介导的基底膜蛋白氧化修饰是正常发育和疾病发病机制中的关键机制。最新进展:过氧化物酶(PXDN)是一种与基底膜相关的动物血红素过氧化物酶,它产生次溴酸(HOBr),在基底膜的IV型胶原网络内形成亚磺酰亚胺交联。这些交联稳定了基底膜,对动物组织发育至关重要。这些发现凸显了次溴酸矛盾的合成代谢作用,它通常会破坏蛋白质结构导致功能障碍。

关键问题

PXDN利用次溴酸作为反应中间体交联IV型胶原,同时避免对附近基底膜蛋白造成附带损伤的分子机制仍不清楚。

未来方向

需要确定基底膜蛋白特定次卤酸介导修饰的确切身份及其功能影响,以便将这些修饰与组织发育和疾病发病机制联系起来。正如IV型胶原的亚磺酰亚胺交联所示,次卤酸氧化事件在某些情况下可能是有益的,而不是一律有害。《抗氧化与氧化还原信号》27卷,839 - 854页 。

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