Active and tissue inhibitor of matrix metalloproteinase-free gelatinase B accumulates within human microvascular endothelial vesicles

被引:75
作者
Nguyen, M [1 ]
Arkell, J [1 ]
Jackson, CJ [1 ]
机构
[1] Royal N Shore Hosp, Sutton Rheumatism Res Lab, St Leonards, NSW 2065, Australia
关键词
D O I
10.1074/jbc.273.9.5400
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
Human gelatinase B is involved in tissue remodeling and angiogenesis, It is thought to be synthesized and rapidly secreted as an inactive precursor. In this report, we have shown that human endothelial cells accumulate active forms of gelatinase B in the cytosol. Microvascular but not macrovascular endothelial cells dramatically increased the expression of cytosolic gelatinase B in response to phorbol myristate acetate, Western blotting showed that tissue inhibitor of metalloproteinase-l (TIMP1) was also present in the cytosol, Whereas gelatinase B was complexed with TIMP1 in the conditioned medium, it existed as a free enzyme in the cytosol, suggesting that the formation of gelatinase B and TIMP1 complex occurs after their secretion, Immunogold electron microscopy revealed that gelatinase B was localized in secretory vesicles which were especially prominent in invading pseudopodia. In contrast, TIMP1 was found throughout the cytoplasm but was not present in the gelatinase vesicles, The accumulation of intracellular activated gelatinase B, ready for rapid release, may facilitate the migration of microvascular endothelial cells during angiogenesis.
引用
收藏
页码:5400 / 5404
页数:5
相关论文
共 35 条
[1]   Expression, subcellular distribution and plasma membrane binding of cathepsin B and gelatinases in bone metastatic tissue [J].
Arkona, C ;
Wiederanders, B .
BIOLOGICAL CHEMISTRY, 1996, 377 (11) :695-702
[2]   Involvement of PA/plasmin system in the processing of pro-MMP-9 and in the second step of pro-MMP-2 activation [J].
Baramova, EN ;
Bajou, K ;
Remacle, A ;
LHoir, C ;
Krell, HW ;
Weidle, UH ;
Noel, A ;
Foidart, JM .
FEBS LETTERS, 1997, 405 (02) :157-162
[4]   EXCESS MATRIX ACCUMULATION IN SCLERODERMA IS CAUSED PARTLY BY DIFFERENTIAL REGULATION OF STROMELYSIN AND TIMP-1 SYNTHESIS [J].
BOUGHARIOS, G ;
OSMAN, J ;
BLACK, C ;
OLSEN, I .
CLINICA CHIMICA ACTA, 1994, 231 (01) :69-78
[5]   Localization of matrix metalloproteinase MMP-2 to the surface of invasive cells by interaction with integrin alpha v beta 3 [J].
Brooks, PC ;
Stromblad, S ;
Sanders, LC ;
vonSchalscha, TL ;
Aimes, RT ;
StetlerStevenson, WG ;
Quigley, JP ;
Cheresh, DA .
CELL, 1996, 85 (05) :683-693
[6]   CELL-SURFACE BINDING OF TIMP-2 AND PRO-MMP-2/TIMP-2 COMPLEX [J].
EMMERTBUCK, MR ;
EMONARD, HP ;
CORCORAN, ML ;
KRUTZSCH, HC ;
FOIDART, JM ;
STETLERSTEVENSON, WG .
FEBS LETTERS, 1995, 364 (01) :28-32
[7]   ANGIOGENESIS IN CANCER, VASCULAR, RHEUMATOID AND OTHER DISEASE [J].
FOLKMAN, J .
NATURE MEDICINE, 1995, 1 (01) :27-31
[8]  
FRIDMAN R, 1995, CANCER RES, V55, P2548
[9]   Urokinase plasminogen activator and gelatinases are associated with membrane vesicles shed by human HT1080 fibrosarcoma cells [J].
Ginestra, A ;
Monea, S ;
Seghezzi, G ;
Dolo, V ;
Nagase, H ;
Mignatti, P ;
Vittorelli, ML .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (27) :17216-17222
[10]  
GOLDBERG GI, 1992, J BIOL CHEM, V267, P4583