Matrix remodeling in the ovary:: regulation and functional role of the plasminogen activator and matrix metalloproteinase systems

被引:114
作者
Ny, T [1 ]
Wahlberg, P [1 ]
Brändström, IJM [1 ]
机构
[1] Umea Univ, Dept Med Biochem & Biophys, S-90187 Umea, Sweden
关键词
ovulation; follicular development; corpus luteum; plasminogen; MMP;
D O I
10.1016/S0303-7207(01)00711-0
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In each reproductive cycle, extensive tissue remodeling takes place in the ovary during follicular development. ovulation. formation and regression of corpus luteum (CL) and Follicular atresia. Several lines of indirect evidence suggest that these changes are mediated, in part. by proteases belonging to the plasminogen activator (PA) and the matrix metalloprotemase (MMP) systems. These two enzyme systems include both proteinases and associated inhibitors, that are thought to act in concert via a cascade of proteolytic events, the end result of which is the generation of a broad spectrum proteolytic activity. that can mediate physiological tissue remodeling throughout the body. The current review, highlights the key features of these two enzyme systems and focuses on their regulation and functional role during the dynamic remodeling processes that takes place in the ovary during each reproductive cycle. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:29 / 38
页数:10
相关论文
共 109 条
[11]   Transcriptional control of matrix metalloproteinases and the tissue inhibitors of matrix metalloproteinases [J].
Borden, P ;
Heller, RA .
CRITICAL REVIEWS IN EUKARYOTIC GENE EXPRESSION, 1997, 7 (1-2) :159-178
[12]   SUPPRESSION OF ICE AND APOPTOSIS IN MAMMARY EPITHELIAL-CELLS BY EXTRACELLULAR-MATRIX [J].
BOUDREAU, N ;
SYMPSON, CJ ;
WERB, Z ;
BISSELL, MJ .
SCIENCE, 1995, 267 (5199) :891-893
[13]   Luteal regression in the normally cycling rat: Apoptosis, monocyte chemoattractant protein-1, and inflammatory cell involvement [J].
Bowen, JM ;
Towns, R ;
Warren, JS ;
Keyes, PL .
BIOLOGY OF REPRODUCTION, 1999, 60 (03) :740-746
[14]   PLASMINOGEN DEFICIENCY CAUSES SEVERE THROMBOSIS BUT IS COMPATIBLE WITH DEVELOPMENT AND REPRODUCTION [J].
BUGGE, TH ;
FLICK, MJ ;
DAUGHERTY, CC ;
DEGEN, JL .
GENES & DEVELOPMENT, 1995, 9 (07) :794-807
[15]   MOUSE OVARIAN GRANULOSA-CELLS PRODUCE UROKINASE-TYPE PLASMINOGEN-ACTIVATOR, WHEREAS THE CORRESPONDING RAT-CELLS PRODUCE TISSUE-TYPE PLASMINOGEN-ACTIVATOR [J].
CANIPARI, R ;
OCONNELL, ML ;
MEYER, G ;
STRICKLAND, S .
JOURNAL OF CELL BIOLOGY, 1987, 105 (02) :977-981
[16]  
CANIPARI R, 1985, J BIOL CHEM, V260, P5121
[17]   Development and disease in proteinase-deficient mice: Role of the plasminogen, matrix metalloproteinase and coagulation system [J].
Carmeliet, P ;
Collen, D .
THROMBOSIS RESEARCH, 1998, 91 (06) :255-285
[18]   PHYSIOLOGICAL CONSEQUENCES OF LOSS OF PLASMINOGEN-ACTIVATOR GENE-FUNCTION IN MICE [J].
CARMELIET, P ;
SCHOONJANS, L ;
KIECKENS, L ;
REAM, B ;
DEGEN, J ;
BRONSON, R ;
DEVOS, R ;
VANDENOORD, JJ ;
COLLEN, D ;
MULLIGAN, RC .
NATURE, 1994, 368 (6470) :419-424
[19]   PLASMINOGEN-ACTIVATOR INHIBITOR-1 GENE DEFICIENT MICE .1. GENERATION BY HOMOLOGOUS RECOMBINATION AND CHARACTERIZATION [J].
CARMELIET, P ;
KIECKENS, L ;
SCHOONJANS, L ;
REAM, B ;
VANNUFFELEN, A ;
PRENDERGAST, G ;
COLE, M ;
BRONSON, R ;
COLLEN, D ;
MULLIGAN, RC .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 92 (06) :2746-2755
[20]   ALPHA-1-ANTITRYPSIN AND THE SERPINS - VARIATION AND COUNTERVARIATION [J].
CARRELL, R ;
TRAVIS, J .
TRENDS IN BIOCHEMICAL SCIENCES, 1985, 10 (01) :20-24