Pathologies of matrix metalloproteinase-2 underactivity: a perspective on a neglected condition

被引:9
作者
Cook, Ryan [1 ]
Sarker, Hassan [1 ]
Fernandez-Patron, Carlos [2 ]
机构
[1] Univ Alberta, Fac Med & Dent, Dept Biochem, 3-19 Med Sci Bldg, Edmonton, AB T6G 2H7, Canada
[2] Univ Alberta, Fac Med & Dent, Dept Biochem, Cardiovasc Res Ctr,Mazankowski Alberta Heart Inst, 3-19 Med Sci Bldg, Edmonton, AB T6G 2H7, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
MMP; inflammation; metabolism; MMP-2; deficiency; TUMOR-NECROSIS-FACTOR; JUVENILE IDIOPATHIC ARTHRITIS; AMYLOID PRECURSOR PROTEIN; MULTICENTRIC OSTEOLYSIS; TISSUE INHIBITOR; GELATINASE-A; 1-MATRIX METALLOPROTEINASE; ENDOGENOUS INHIBITORS; ENDOTHELIAL-CELLS; ARTHROPATHY MONA;
D O I
10.1139/cjpp-2018-0525
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A member of the matrix metalloproteinase family, matrix metalloproteinase-2 (MMP-2, gelatinase A), has been extensively studied for its role in both normal physiology and pathological processes. Whereas most research efforts in recent years have investigated the pathologies associated with MMP-2 overactivity, the pathological mechanisms elicited by MMP-2 underactivity are less well understood. Here, we distinguish between 2 states and describe their causes: (i) MMP-2 deficiency (complete loss of MMP-2 activity) and (ii) MMP-2 insufficiency (defined as MMP-2 activity below baseline levels). Further, we review the biology of MMP-2, summarizing the current literature on MMP-2 underactivity in both mice and humans, and describe research being conducted by our lab towards improving our understanding of the pathological mechanisms elicited by MMP-2 deficiency/insufficiency. We think that this research could stimulate the discovery of new therapeutic approaches for managing pathologies associated with MMP-2 underactivity. Moreover, similar concepts could apply to other members of the matrix metalloproteinase family.
引用
收藏
页码:486 / 492
页数:7
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