Messenger RNA for membrane-type 2 matrix metalloproteinase, MT2-MMP, is expressed in human placenta of first trimester

被引:41
作者
Bjorn, SF
Hastrup, N
Larsen, JF
Lund, LR
Pyke, C
机构
[1] Rigshosp, Finsen Lab, DK-2100 Copenhagen O, Denmark
[2] Herlev Univ Hosp, Dept Obstet & Gynecol, DK-2730 Herlev, Denmark
[3] Herlev Univ Hosp, Dept Pathol, DK-2730 Herlev, Denmark
[4] Novo Nordisk AS, Histol, DK-2880 Bagsvaerd, Denmark
关键词
D O I
10.1053/plac.1999.0447
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
An intimately regulated cell surface activation of matrix metalloproteinases (MMPs) is believed to be of critical importance for the control of trophoblast invasion. A histological investigation of the expression and localization of three different MMPs, the membrane-type matrix metalloproteinases 1 and 2 (MT1-MMP, MT2-MMP) and matrix metalloproteinase 2 (MMP-2/gelatinase A) was performed by in situ hybridization on consecutive sections from human placentae of first trimester pregnancies. Cytokeratin immunostaining identified trophoblast cells. Both normal and tubal implantation sites were studied. We observed a high degree of coexpression of MT2-MMP, MT1-MMP and MMP-2 mRNAs in single extravillous cytotrophoblasts that had invaded the endometrium and tubal wall. Furthermore, mRNAs for all three genes were also seen in cytotrophoblasts of cell islands. In contrast to this coexpression pattern, MT2-MMP expression was absent from cell columns and decidual cells, in which signals for MT1-MMP and MMP-2 mRNAs were seen. The present data on the cellular expression of MT2-MMP mRNA in placenta extend our knowledge of the proteolytic events that take place during early pregnancy. The data suggest that MT2-MMP, capable of activating MMP-2 in vitro, is involved in the invasion of extravillous cytotrophoblast, possibly related to the physiological activation of MMP-2. (C) 2000 Harcourt Publishers Ltd.
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页码:170 / 176
页数:7
相关论文
共 41 条
[1]  
Benirschke K., 1995, Pathology of the Human Placenta. Pathology of the Human Placenta
[2]   MATRIX METALLOPROTEINASES - A REVIEW [J].
BIRKEDALHANSEN, H ;
MOORE, WGI ;
BODDEN, MK ;
WINDSOR, LJ ;
BIRKEDALHANSEN, B ;
DECARLO, A ;
ENGLER, JA .
CRITICAL REVIEWS IN ORAL BIOLOGY & MEDICINE, 1993, 4 (02) :197-250
[3]   Co-ordinated expression of MMP-2 and its putative activator, MT1-MMP, in human placentation [J].
Bjorn, SF ;
Hastrup, N ;
Lund, LR ;
Dano, K ;
Larsen, JF ;
Pyke, C .
MOLECULAR HUMAN REPRODUCTION, 1997, 3 (08) :713-723
[4]   GENES FOR EXTRACELLULAR MATRIX-DEGRADING METALLOPROTEINASES AND THEIR INHIBITOR, TIMP, ARE EXPRESSED DURING EARLY MAMMALIAN DEVELOPMENT [J].
BRENNER, CA ;
ADLER, RR ;
RAPPOLEE, DA ;
PEDERSEN, RA ;
WERB, Z .
GENES & DEVELOPMENT, 1989, 3 (06) :848-859
[5]   The TIMP2 membrane type 1 metalloproteinase "receptor" regulates the concentration and efficient activation of progelatinase A - A kinetic study [J].
Butler, GS ;
Butler, MJ ;
Atkinson, SJ ;
Will, H ;
Tamura, T ;
van Westrum, SS ;
Crabbe, T ;
Clements, J ;
d'Ortho, MP ;
Murphy, G .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (02) :871-880
[6]   Membrane-type-2 matrix metalloproteinase can initiate the processing of progelatinase A and is regulated by the tissue inhibitors of metalloproteinases [J].
Butler, GS ;
Will, H ;
Atkinson, SJ ;
Murphy, G .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1997, 244 (02) :653-657
[7]   Membrane-type matrix metalloproteinases 1 and 2 exhibit broad-spectrum proteolytic capacities comparable to many matrix metalloproteinases [J].
d'Ortho, MP ;
Will, H ;
Atkinson, S ;
Butler, G ;
Messent, A ;
Gavrilovic, J ;
Smith, B ;
Timpl, R ;
Zardi, L ;
Murphy, G .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1997, 250 (03) :751-757
[8]   Induction of cell migration by matrix metalloprotease-2 cleavage of laminin-5 [J].
Giannelli, G ;
FalkMarzillier, J ;
Schiraldi, O ;
StetlerStevenson, WG ;
Quaranta, V .
SCIENCE, 1997, 277 (5323) :225-228
[9]   ESTABLISHMENT AND CHARACTERIZATION OF 1ST TRIMESTER HUMAN TROPHOBLAST CELLS WITH EXTENDED LIFE-SPAN [J].
GRAHAM, CH ;
HAWLEY, TS ;
HAWLEY, RG ;
MACDOUGALL, JR ;
KERBEL, RS ;
KHOO, N ;
LALA, PK .
EXPERIMENTAL CELL RESEARCH, 1993, 206 (02) :204-211
[10]   MECHANISM OF CONTROL OF TROPHOBLAST INVASION INSITU [J].
GRAHAM, CH ;
LALA, PK .
JOURNAL OF CELLULAR PHYSIOLOGY, 1991, 148 (02) :228-234