Homotrimeric MMP-9 is an active hitchhiker on alpha-2-macroglobulin partially escaping protease inhibition and internalization through LRP-1

被引:27
作者
Serifova, Xena [1 ]
Ugarte-Berzal, Estefania [1 ]
Opdenakker, Ghislain [1 ]
Vandooren, Jennifer [1 ]
机构
[1] Univ Leuven, Rega Inst Med Res, Dept Microbiol & Immunol, Lab Immunobiol,KU Leuven, Herestr 49,Bus 1044, B-3000 Leuven, Belgium
关键词
Proteolysis; alpha; 2M; MMP-9; Endocytosis; LRP-1; GELATINASE B/MATRIX METALLOPROTEINASE-9; MATRIX METALLOPROTEINASES; ALPHA(2) MACROGLOBULIN; SIGNAL-TRANSDUCTION; ALPHA(2)-MACROGLOBULIN; BINDING; MATRIX-METALLOPROTEINASE-9; PLASMA; ALPHA2-MACROGLOBULIN; PROLIFERATION;
D O I
10.1007/s00018-019-03338-4
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
Proteolysis is a crucial process in life, tightly controlled by numerous natural protease inhibitors. In human blood, alpha-2-macroglobulin is an emergency protease inhibitor preventing coagulation and damage to endothelia and leukocytes. With the use of a unique protease trapping mechanism, alpha-2-macroglobulin lures active proteases into its snap-trap, shields these from potential substrates and 'flags' their complex for elimination by receptor-mediated endocytosis. Matrix metalloprotease-9/gelatinase B is a secreted protease increased in blood of patients with inflammations, vascular disorders and cancers. Matrix metalloprotease-9 occurs as monomers and stable homotrimers, but the reason for their co-existence remains obscure. We discovered that matrix metalloprotease-9 homotrimers undergo reduced anti-proteolytic regulation by alpha-2-macroglobulin and are able to travel as a proteolytically active hitchhiker on alpha-2-macroglobulin. As a comparison, we revealed that monomeric active matrix metalloprotease-9 is efficiently trapped by human plasma alpha-2-macroglobulin and this masks the detection of activated matrix metalloprotease-9 with standard analysis techniques. In addition, we show that alpha-2-macroglobulin/trimer complexes escape clearance through the receptor low-density lipoprotein receptor-related protein 1, also known as the alpha-2-macroglobulin receptor. Thus, the biochemistry and biology of matrix metalloprotease-9 monomers and trimers are completely different as multimerization enables active matrix metalloprotease-9 to partially avoid alpha-2-macroglobulin regulation both by direct protease inhibition and by removal from the extracellular space by receptor-mediated endocytosis. Finally, for the biomarker field, the analysis of alpha-2-macroglobulin/protease complexes with upgraded technology is advocated as a quotum for protease activation in human plasma samples.
引用
收藏
页码:3013 / 3026
页数:14
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