Collagen VI in the Musculoskeletal System

被引:28
作者
Di Martino, Alberto [1 ,2 ]
Cescon, Matilde [3 ]
D'Agostino, Claudio [1 ,2 ]
Schilardi, Francesco [1 ,2 ]
Sabatelli, Patrizia [4 ,5 ]
Merlini, Luciano [2 ]
Faldini, Cesare [1 ,2 ]
机构
[1] IRCCS Ist Ortoped Rizzoli, Orthoped & Traumatol Dept 1, I-40136 Bologna, Italy
[2] Univ Bologna, Dept Biomed & Neuromotor Sci, DIBINEM, I-40136 Bologna, Italy
[3] Univ Padua, Dept Mol Med, I-35131 Padua, Italy
[4] Unit Bologna, CNR Inst Mol Genet Luigi Luca Cavalli Sforza, I-40136 Bologna, Italy
[5] IRCCS Ist Ortoped Rizzoli, I-40136 Bologna, Italy
关键词
collagen type VI; Ullrich congenital muscular dystrophy; Bethlem myopathy; myosclerosis myopathy; animal models; orthopedic surgery; limb deformities; POSTERIOR LONGITUDINAL LIGAMENT; CONGENITAL MUSCULAR-DYSTROPHY; AUTOSOMAL-DOMINANT MYOPATHY; EHLERS-DANLOS-SYNDROME; BETHLEM MYOPATHY; ARTICULAR-CARTILAGE; MITOCHONDRIAL DYSFUNCTION; ALPHA-3(VI) CHAIN; SKELETAL-MUSCLE; EXTRACELLULAR-MATRIX;
D O I
10.3390/ijms24065095
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Collagen VI exerts several functions in the tissues in which it is expressed, including mechanical roles, cytoprotective functions with the inhibition of apoptosis and oxidative damage, and the promotion of tumor growth and progression by the regulation of cell differentiation and autophagic mechanisms. Mutations in the genes encoding collagen VI main chains, COL6A1, COL6A2 and COL6A3, are responsible for a spectrum of congenital muscular disorders, namely Ullrich congenital muscular dystrophy (UCMD), Bethlem myopathy (BM) and myosclerosis myopathy (MM), which show a variable combination of muscle wasting and weakness, joint contractures, distal laxity, and respiratory compromise. No effective therapeutic strategy is available so far for these diseases; moreover, the effects of collagen VI mutations on other tissues is poorly investigated. The aim of this review is to outline the role of collagen VI in the musculoskeletal system and to give an update about the tissue-specific functions revealed by studies on animal models and from patients' derived samples in order to fill the knowledge gap between scientists and the clinicians who daily manage patients affected by collagen VI-related myopathies.
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页数:22
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