BMP-1/tolloid-like proteinases synchronize matrix assembly with growth factor activation to promote rnorphogenesis and tissue remodeling

被引:111
作者
Vadon-Le Goff, Sandrine [1 ]
Hulmes, David J. S. [1 ]
Moali, Catherine [1 ]
机构
[1] Univ Lyon, CNRS, UMR 5305, Lab Biol Tissulaire & Ingn Therapeut, F-69367 Lyon, France
关键词
Metalloproteinase; Collagen; Bone morphogenetic protein; TGF-beta; Osteogenesis imperfecta; Fibrosis; PROCOLLAGEN-C-PROTEINASE; BONE MORPHOGENETIC PROTEIN-1; DENTIN SIALOPHOSPHOPROTEIN DSPP; FRIZZLED-RELATED PROTEIN-2; I PROCOLLAGEN; LYSYL OXIDASE; ENHANCER PROTEIN; UP-REGULATION; METALLOPROTEINASE ACTIVITY; COLLAGEN FIBRILLOGENESIS;
D O I
10.1016/j.matbio.2015.02.006
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
Bone morphogenetic protein-1 (BMP-1)/tolloid-like proteinases, here called BTPs, include the proteases originally identified for their roles in the C-terminal maturation of fibrillar procollagens ("pocollagen C-proteinase"). Though numerous other substrates have since been discovered, the BTPs remain the main proteases involved in extracellular matrix assembly with little or no implication in matrix degradation. During the same period however, the BTPs have also become established as important proteases in the activation of growth factors, including TGF-beta 1, BMP-2/-4, GDF-8/-11 and IGFs, as well as the release of anti-angiogenic fragments from parent proteins. The BTPs are therefore key players in many pathophysiological processes such as morphogenesis, tissue repair and tumor progression. This mini-review summarizes our current knowledge of the functions of BTPs, their substrates and unusual mechanisms of regulation, and discusses their potential as new targets for future therapies. (C) 2015 Elsevier B.V.
引用
收藏
页码:14 / 23
页数:10
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