胶原VI
细胞外基质
肌营养不良
先天性肌营养不良
胶原蛋白,I型,α1
心肌细胞
Ⅰ型胶原
成纤维细胞
免疫印迹
化学
骨骼肌
ITGA7型
细胞外
间质细胞
细胞生物学
病理
生物
分子生物学
体外
内分泌学
医学
生物化学
遗传学
基因
作者
Yaqun Zou,Rui-Zhu Zhang,Patrizia Sabatelli,M. L. Chu,Carsten G. Bönnemann
标识
DOI:10.1097/nen.0b013e3181634ef7
摘要
Mutations in the extracellular matrix molecule collagen VI underlie the congenital muscular dystrophy types Ullrich and Bethlem. Establishing the origin of collagen VI in muscle is important for understanding the pathophysiology of these diseases and for developing future treatment approaches involving cell-specific delivery. Because the cells that produce collagen VI cannot be identified by histologic analysis, we examined the production of collagen VI in pure cultures of primary myogenic cells and muscle interstitial fibroblasts from limb muscle of neonatal mice. Immunofluorescence staining and Western blot analysis revealed secretion and matrix deposition of collagen VI by interstitial fibroblasts but not by myogenic cells in vitro. Using Northern blot and real-time reverse-transcriptase-polymerase chain reaction analysis for the collagen VI genes col6a1, col6a2, col6a3, transcript levels for the 3 mRNAs were high in interstitial fibroblasts, whereas in primary myogenic cells, they were indistinguishable from background. Furthermore, retention of mutant collagen VI in muscle from 3 patients with collagen VI mutation was identified in interstitial fibroblastic cells but not in their myofibers. These results suggest that interstitial fibroblasts but not myogenic cells contribute significantly to the deposition of collagen VI in the extracellular matrix in skeletal muscle and imply major roles of this cell type and the extracellular matrix in the pathogenesis of these diseases.
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