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WARP:软骨、肌肉和血管内皮细胞基底膜的独特细胞外基质成分。

WARP: A Unique Extracellular Matrix Component of Cartilage, Muscle, and Endothelial Cell Basement Membranes.

机构信息

Department of Orthopedic Surgery, Bone and Joint Center, Henry Ford Hospital System, Detroit, Michigan.

出版信息

Anat Rec (Hoboken). 2020 Jun;303(6):1619-1623. doi: 10.1002/ar.24087. Epub 2019 Mar 5.

DOI:10.1002/ar.24087
PMID:30768857
Abstract

The von Willebrand factor A-domain-related protein (WARP) encoded by the VWA1 gene, is an orphan extracellular matrix protein that is expressed in a subset of ECM structures but whose function is poorly understood. Here, recent advances on understanding VWA1/WARP will be reviewed including analysis of VWA1 reporter and global knock-out mice, interaction studies, and recent transcriptome analyses. Anat Rec, 2019. © 2019 Wiley Periodicals, Inc.

摘要

VWA1 基因编码的血管性血友病因子 A 结构域相关蛋白(WARP)是一种孤儿细胞外基质蛋白,在一部分 ECM 结构中表达,但功能知之甚少。本文将综述近年来对 VWA1/WARP 的认识进展,包括 VWA1 报告基因和全局敲除小鼠分析、相互作用研究和最近的转录组分析。解剖学记录,2019。© 2019 威利父子出版公司

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WARP: A Unique Extracellular Matrix Component of Cartilage, Muscle, and Endothelial Cell Basement Membranes.WARP:软骨、肌肉和血管内皮细胞基底膜的独特细胞外基质成分。
Anat Rec (Hoboken). 2020 Jun;303(6):1619-1623. doi: 10.1002/ar.24087. Epub 2019 Mar 5.
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The extracellular matrix protein WARP is a novel component of a distinct subset of basement membranes.细胞外基质蛋白WARP是基底膜一个独特亚群的新型成分。
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Mice lacking the extracellular matrix protein WARP develop normally but have compromised peripheral nerve structure and function.缺乏细胞外基质蛋白WARP的小鼠发育正常,但外周神经结构和功能受损。
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WARP is a novel multimeric component of the chondrocyte pericellular matrix that interacts with perlecan.WARP是软骨细胞周细胞外基质的一种新型多聚体成分,可与基底膜聚糖相互作用。
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Genetic Suppression of Basement Membrane Defects in by Gain of Function in Extracellular Matrix and Cell-Matrix Attachment Genes.通过细胞外基质和细胞-基质黏附基因功能获得,抑制 中的基底膜缺陷。
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WARP interacts with collagen VI-containing microfibrils in the pericellular matrix of human chondrocytes.WARP 与人类软骨细胞细胞周基质中含有胶原 VI 的微纤维相互作用。
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Focus on molecules: perlecan (HSPG2).聚焦分子:基底膜聚糖(HSPG2)。
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An ancestral 10-bp repeat expansion in VWA1 causes recessive hereditary motor neuropathy.VWA1 中的一个祖先 10-bp 重复扩展导致隐性遗传性运动神经病。
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