Plasminogen activator inhibitor 1 is an intracellular inhibitor of furin proprotein convertase

被引:37
作者
Bernot, Denis [1 ]
Stalin, Jimmy [1 ]
Stocker, Pierre [2 ]
Bonardo, Bernadette [1 ]
Scroyen, Ilse [1 ]
Alessi, Marie-Christine [1 ]
Peiretti, Franck [1 ]
机构
[1] Univ Aix Marseille 2, INSERM, Fac Med, U626, F-13385 Marseille 5, France
[2] Univ Paul Cezanne, Equipe Biosci iSm2 UMR 6263, FST St Jerome, F-13397 Marseille 20, France
关键词
ADAM17; Furin; Golgi; Insulin receptor; PAI-1; Convertase; NECROSIS-FACTOR-ALPHA; TRANSMEMBRANE TNF-ALPHA; INSULIN-RESISTANCE; ADIPOSE-TISSUE; ENDOTHELIAL-CELLS; SECRETORY PATHWAY; ENDOGENOUS FURIN; CUTTING EDGE; ENZYME; SERPIN;
D O I
10.1242/jcs.079889
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Proprotein convertases (PCs) are a family of serine proteases that are involved in the post-translational processing and activation of a wide range of regulatory proteins. The upstream role of PCs in the control of many physiological and pathological processes generates a growing interest in understanding their regulation. Here, we demonstrate that the serine protease inhibitor plasminogen activator inhibitor 1 (PAI-1) forms an SDS-stable complex with the PC furin, which leads to the inhibition of the intra-Golgi activity of furin. It is known that elevated PAI-1 plasma levels are correlated with the occurrence of the metabolic syndrome and type 2 diabetes, and we show that PAI-1 reduces the furin-dependent maturation and activity of the insulin receptor and ADAM17: two proteins involved in the onset of these metabolic disorders. In addition to demonstrating that PAI-1 is an intracellular inhibitor of furin, this study also provides arguments in favor of an active role for PAI-1 in the development of metabolic disorders.
引用
收藏
页码:1224 / 1230
页数:7
相关论文
共 53 条
[1]   Metabolic syndrome, haemostasis and thrombosis [J].
Alessi, Marie-Christine ;
Juhan-Vague, Irene .
THROMBOSIS AND HAEMOSTASIS, 2008, 99 (06) :995-1000
[2]   Rasminogen activator inhibitor-1, adipose tissue and insulin resistance [J].
Alessi, Marie-Christine ;
Poggi, Marjorie ;
Juhan-Vague, Irene .
CURRENT OPINION IN LIPIDOLOGY, 2007, 18 (03) :240-245
[3]   Production of plasminogen activator inhibitor 1 by human adipose tissue - Possible link between visceral fat accumulation and vascular disease [J].
Alessi, MC ;
Peiretti, F ;
Morange, P ;
Henry, M ;
Nalbone, G ;
JuhanVague, I .
DIABETES, 1997, 46 (05) :860-867
[4]   Activation of the furin endoprotease is a multiple-step process: Requirements for acidification and internal propeptide cleavage [J].
Anderson, ED ;
VanSlyke, JK ;
Thulin, CD ;
Jean, F ;
Thomas, G .
EMBO JOURNAL, 1997, 16 (07) :1508-1518
[5]  
ANDERSON ED, 1993, J BIOL CHEM, V268, P24887
[6]   alpha 1-antitrypsin portland inhibits processing of precursors mediated by proprotein convertases primarily within the constitutive secretory pathway [J].
Benjannet, S ;
Savaria, D ;
Laslop, A ;
Munzer, JS ;
Chretien, M ;
Marcinkiewicz, M ;
Seidah, NG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (42) :26210-26218
[7]   A metalloproteinase disintegrin that releases tumour-necrosis factor-alpha from cells [J].
Black, RA ;
Rauch, CT ;
Kozlosky, CJ ;
Peschon, JJ ;
Slack, JL ;
Wolfson, MF ;
Castner, BJ ;
Stocking, KL ;
Reddy, P ;
Srinivasan, S ;
Nelson, N ;
Boiani, N ;
Schooley, KA ;
Gerhart, M ;
Davis, R ;
Fitzner, JN ;
Johnson, RS ;
Paxton, RJ ;
March, CJ ;
Cerretti, DP .
NATURE, 1997, 385 (6618) :729-733
[8]   FURIN HAS THE PROALBUMIN SUBSTRATE-SPECIFICITY AND SERPIN INHIBITORY PROPERTIES OF AN IN-SITU HEPATIC CONVERTASE [J].
BRENNAN, SO ;
NAKAYAMA, K .
FEBS LETTERS, 1994, 338 (02) :147-151
[9]   Identification of inhibitors using a cell-based assay for monitoring Golgi-resident protease activity [J].
Coppola, Julia M. ;
Hamilton, Christin A. ;
Bhojani, Mahaveer S. ;
Larsen, Martha J. ;
Ross, Brian D. ;
Rehemtulla, Alnawaz .
ANALYTICAL BIOCHEMISTRY, 2007, 364 (01) :19-29
[10]   Inhibition of soluble recombinant furin by human proteinase inhibitor 8 [J].
Dahlen, JR ;
Jean, F ;
Thomas, G ;
Foster, DC ;
Kisiel, W .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (04) :1851-1854