基质刚度的压电依赖性监视产生修复基膜的瞬态细胞

IF 10.7 1区 生物学 Q1 CELL BIOLOGY
Aubrie M. Stricker, M. Shane Hutson, Andrea Page-McCaw
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引用次数: 0

摘要

基底膜是分离组织层并提供机械支持的细胞外基质片,胶原IV (Col4)是其最丰富的结构蛋白。尽管基底膜在损伤后可以修复,但对修复知之甚少,包括是否以及如何检测损伤,哪些细胞修复损伤,以及如何控制修复以避免纤维化。以成年果蝇的肠基底膜为模型,我们发现基底膜损伤后,瞬时表达Col4的肠母细胞急剧增加,称为“基质修补”细胞。肠母细胞衍生的Col4是基质修复所特别需要的。基质修补细胞的增加需要在肠干细胞中表达的机械敏感离子通道Piezo。由于特异性抑制Col4交联足以诱导基质修补细胞的压电依赖性诱导,基质修补细胞是由基体刚度的损失诱导的。我们的数据表明上皮干细胞通过监测刚度来控制基底膜的完整性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Piezo-dependent surveillance of matrix stiffness generates transient cells that repair the basement membrane

Piezo-dependent surveillance of matrix stiffness generates transient cells that repair the basement membrane
Basement membranes are extracellular matrix sheets separating tissue layers and providing mechanical support, and collagen IV (Col4) is their most abundant structural protein. Although basement membranes are repaired after damage, little is known about repair, including whether and how damage is detected, what cells repair the damage, and how repair is controlled to avoid fibrosis. Using the intestinal basement membrane of adult Drosophila as a model, we show that after basement membrane damage, there is a sharp increase in enteroblasts transiently expressing Col4, termed “matrix mender” cells. Enteroblast-derived Col4 is specifically required for matrix repair. The increase in matrix mender cells requires the mechanosensitive ion channel Piezo, expressed in intestinal stem cells. Matrix menders are induced by the loss of matrix stiffness, as specifically inhibiting Col4 crosslinking is sufficient for Piezo-dependent induction of matrix mender cells. Our data suggest that epithelial stem cells control basement membrane integrity by monitoring stiffness.
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来源期刊
Developmental cell
Developmental cell 生物-发育生物学
CiteScore
18.90
自引率
1.70%
发文量
203
审稿时长
3-6 weeks
期刊介绍: Developmental Cell, established in 2001, is a comprehensive journal that explores a wide range of topics in cell and developmental biology. Our publication encompasses work across various disciplines within biology, with a particular emphasis on investigating the intersections between cell biology, developmental biology, and other related fields. Our primary objective is to present research conducted through a cell biological perspective, addressing the essential mechanisms governing cell function, cellular interactions, and responses to the environment. Moreover, we focus on understanding the collective behavior of cells, culminating in the formation of tissues, organs, and whole organisms, while also investigating the consequences of any malfunctions in these intricate processes.
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