High resolution three‐dimensional reconstruction of fibrotic skeletal muscle extracellular matrix

Allison R Gillies, Mark A. Chapman, E. Bushong, T. Deerinck, Mark Ellisman, R. Lieber
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引用次数: 45

Abstract

Fibrosis occurs secondary to many skeletal muscle diseases and injuries, and can alter muscle function. It is unknown how collagen, the most abundant extracellular structural protein, alters its organization during fibrosis. Quantitative and qualitative high‐magnification electron microscopy shows that collagen is organized into perimysial cables which increase in number in a model of fibrosis, and cables have unique interactions with collagen‐producing cells. Fibrotic muscles are stiffer and have a higher concentration of collagen‐producing cells. These results improve our understanding of the organization of fibrotic skeletal muscle extracellular matrix and identify novel structures that might be targeted by antifibrotic therapy.
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纤维化骨骼肌细胞外基质的高分辨率三维重建
纤维化继发于许多骨骼肌疾病和损伤,可改变肌肉功能。胶原蛋白是最丰富的细胞外结构蛋白,在纤维化过程中如何改变其组织结构尚不清楚。定量和定性高倍率电子显微镜显示,在纤维化模型中,胶原蛋白被组织成膜周索,其数量增加,并且索与胶原蛋白产生细胞有独特的相互作用。纤维化肌肉更硬,产生胶原蛋白的细胞浓度更高。这些结果提高了我们对纤维化骨骼肌细胞外基质组织的理解,并确定了可能被抗纤维化治疗靶向的新结构。
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