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肠道内稳态、损伤与修复:新的治疗靶点。

Gut homeostasis, injury, and healing: New therapeutic targets.

机构信息

Department of Biomedical Sciences, University of North Dakota School of Medicine and Health Sciences, Grand Forks, ND 58202, United States.

出版信息

World J Gastroenterol. 2022 May 7;28(17):1725-1750. doi: 10.3748/wjg.v28.i17.1725.

Abstract

The integrity of the gastrointestinal mucosa plays a crucial role in gut homeostasis, which depends upon the balance between mucosal injury by destructive factors and healing protective factors. The persistence of noxious agents such as acid, pepsin, nonsteroidal anti-inflammatory drugs, or breaks down the mucosal barrier and injury occurs. Depending upon the size and site of the wound, it is healed by complex and overlapping processes involving membrane resealing, cell spreading, purse-string contraction, restitution, differentiation, angiogenesis, and vasculogenesis, each modulated by extracellular regulators. Unfortunately, the gut does not always heal, leading to such pathology as peptic ulcers or inflammatory bowel disease. Currently available therapeutics such as proton pump inhibitors, histamine-2 receptor antagonists, sucralfate, 5-aminosalicylate, antibiotics, corticosteroids, and immunosuppressants all attempt to minimize or reduce injury to the gastrointestinal tract. More recent studies have focused on improving mucosal defense or directly promoting mucosal repair. Many investigations have sought to enhance mucosal defense by stimulating mucus secretion, mucosal blood flow, or tight junction function. Conversely, new attempts to directly promote mucosal repair target proteins that modulate cytoskeleton dynamics such as tubulin, talin, Ehm, filamin-a, gelsolin, and flightless I or that proteins regulate focal adhesions dynamics such as focal adhesion kinase. This article summarizes the pathobiology of gastrointestinal mucosal healing and reviews potential new therapeutic targets.

摘要

胃肠道黏膜的完整性对于肠道内稳态至关重要,这取决于破坏性因素引起的黏膜损伤与愈合保护因素之间的平衡。酸、胃蛋白酶、非甾体抗炎药或其他有害物质的持续存在会破坏黏膜屏障并导致损伤。根据伤口的大小和部位,它通过涉及膜重封、细胞扩散、荷包缝合收缩、恢复、分化、血管生成和血管发生的复杂和重叠过程来愈合,每个过程都受到细胞外调节剂的调节。不幸的是,肠道并不总是能够愈合,导致消化性溃疡或炎症性肠病等病理学改变。目前可用的治疗方法,如质子泵抑制剂、H2 受体拮抗剂、硫糖铝、5-氨基水杨酸、抗生素、皮质类固醇和免疫抑制剂,都试图最大限度地减少或减轻胃肠道损伤。最近的研究集中在改善黏膜防御或直接促进黏膜修复上。许多研究试图通过刺激黏液分泌、黏膜血流或紧密连接功能来增强黏膜防御。相反,直接促进黏膜修复的新尝试针对的是调节细胞骨架动力学的蛋白质,如微管蛋白、talin、Ehm、细丝蛋白-a、凝胶蛋白和无翅 I 或调节黏着斑动力学的蛋白质,如黏着斑激酶。本文总结了胃肠道黏膜愈合的病理生物学,并回顾了潜在的新治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b67/9099196/f3dc71cb2fa9/WJG-28-1725-g001.jpg

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