Cysteine cathepsins in extracellular matrix remodeling: Extracellular matrix degradation and beyond

被引:117
|
作者
Vizovisek, Matej [1 ]
Fonovic, Marko [1 ]
Turk, Boris [1 ,2 ]
机构
[1] Jozef Stefan Inst, Dept Biochem & Mol & Struct Biol, Jamova Cesta 39, SI-1000 Ljubljana, Slovenia
[2] Univ Ljubljana, Fac Chem & Chem Technol, Vecna Pot 113, SI-1000 Ljubljana, Slovenia
关键词
Cysteine cathepsins; Extracellular milieu; ECM remodeling and signaling; Disease; BASEMENT-MEMBRANE DEGRADATION; PH-INDUCED INACTIVATION; DIPEPTIDYL PEPTIDASE-I; HUMAN PROCATHEPSIN B; ELASTIN DEGRADATION; CANCER PROGRESSION; PROTEASE ACTIVITY; PROTEOMIC IDENTIFICATION; PLASMINOGEN-ACTIVATOR; BONE-RESORPTION;
D O I
10.1016/j.matbio.2018.01.024
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
Cysteine cathepsins have been for a long time considered to execute mainly nonspecific bulk proteolysis in the endolysosomal system. However, this view has been changing profoundly over the last decade as cathepsins were found in the cytoplasm, nucleus and in the extracellular milieu. Cathepsins are currently gaining increased attention largely because of their extracellular roles associated with disease development and progression. While kept under tight control under physiological conditions, their dysregulated and elevated activity in the extracellular milieu are distinctive hallmarks of numerous diseases such as various cancers, inflammatory disorders, rheumatoid arthritis, bone disorders and heart diseases. In this review, we discuss cysteine cathepsins with a major focus on their extracellular roles and extracellular proteolytic targets beyond degradation of the extracellular matrix. We further highlight the perspectives of cathepsin research and novel avenues in cathepsin-based diagnostic and therapeutic applications. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:141 / 159
页数:19
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