Matrix metalloproteinase expression and function during fin regeneration in zebrafish: Analysis of MT1-MMP, MMP2 and TIMP2

被引:83
作者
Bai, S
Thummel, R
Godwin, AR
Nagase, H
Itoh, Y
Li, L
Evans, R
McDermott, J
Seiki, M
Sarras, MP
机构
[1] Rosalind Franklin Univ Med & Sci, Chicago Med Sch, Dept Cell Biol & Anat, N Chicago, IL 60064 USA
[2] Univ Kansas, Med Ctr, Dept Anat & Cell Biol, Kansas City, KS 66160 USA
[3] Univ Kansas, Med Ctr, Dept Mol & Integrat Physiol, Kansas City, KS 66160 USA
[4] Univ London Imperial Coll Sci & Technol, Fac Med, Kennedy Inst Rheumatol Div, London, England
[5] Univ Tokyo, Div Canc Cell Res, Minato Ku, Tokyo 1088630, Japan
基金
英国惠康基金;
关键词
matrix metalloproteinases; MT1-MMP; zebrafish; fin regeneration; ECM;
D O I
10.1016/j.matbio.2005.03.007
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
Matrix metalloproteinases (MMPs) play key roles in the turnover of extracellular matrix (ECM) and, thereby, function as key regulators of cell-ECM interactions during development. In spite of their importance during developmental processes, relatively little has been reported about the role of these metalloproteinases during limb development and regeneration. To approach the problem of cell-ECM interactions during limb (fin) regeneration, we have utilized zebrafish as an experimental model. Based on previous MMP cloning studies from our laboratory, the current study has focused on the expression of membrane-type I metalloproteinase (MT1-MMP), gelatinase A (MMP-2) and endogenous tissue inhibitor 2 of metalloproteinases (TIMP-2) during fin regeneration in adult zebrafish. In situ analysis indicated co-expression of zmt1-mmp, zmmp-2, and ztimp-2 mRNA transcripts in regenerating caudal fins. In situ gelatin-zymography confirmed the presence of active metalloproteinases in regenerating fins. zmt1-mmp, zmmp-2, and ztimp-2 mRNA transcripts were expressed in the blastema and basal epithelium during caudal fin regeneration while expression of type IV collagen [zcol-IV(a5)] transcripts (a basal lamina component) was restricted to the basal epithelium. Fin outgrowth was greatly reduced in the presence of GM6001 (an inhibitor of MMP activity) indicating the importance of these enzymes during fin regeneration. Previous studies by Itch (EMBO, 2001) indicated that expression of a vertebrate MT1-MMP construct containing only the hemopexin-transmembrane-cytoplasmic domains (MT1HPX) resulted in blockage of MT1-MMP homophilic complex formation and subsequent inhibition of pro-MMP-2 activation. Interference with homophilic complex formation was attributed to expression of the hemopexin domain at the cell surface. Building upon these earlier findings, the current study found that ectopic expression of MT1HPX in fin regenerates inhibited the regeneration process and resulted in a reduction in cell proliferation in the blastema. Taken together, these results indicate that MMPs have an important role during fin regeneration in zebrafish. (c) 2005 Elsevier B.V/Intemational Society of Matrix Biology. All rights reserved.
引用
收藏
页码:247 / 260
页数:14
相关论文
共 57 条
  • [1] AKIMENKO MA, 1995, DEVELOPMENT, V121, P347
  • [2] The matrix metalloproteinase-14 (MMP-14) gene is structurally distinct from other MMP genes and is co-expressed with the TIMP-2 gene during mouse embryogenesis
    Apte, SS
    Fukai, N
    Beier, DR
    Olsen, BR
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (41) : 25511 - 25517
  • [3] Tissue inhibitors of metalloproteinases: evolution, structure and function
    Brew, K
    Dinakarpandian, D
    Nagase, H
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-PROTEIN STRUCTURE AND MOLECULAR ENZYMOLOGY, 2000, 1477 (1-2): : 267 - 283
  • [4] BROUSSANT M, HIST ACAD ROY SCIENC
  • [5] The TIMP2 membrane type 1 metalloproteinase "receptor" regulates the concentration and efficient activation of progelatinase A - A kinetic study
    Butler, GS
    Butler, MJ
    Atkinson, SJ
    Will, H
    Tamura, T
    van Westrum, SS
    Crabbe, T
    Clements, J
    d'Ortho, MP
    Murphy, G
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (02) : 871 - 880
  • [6] Colognato H, 2000, DEV DYNAM, V218, P213, DOI 10.1002/(SICI)1097-0177(200006)218:2<213::AID-DVDY1>3.0.CO
  • [7] 2-R
  • [8] D'Angelo M, 2000, J CELL BIOCHEM, V77, P678, DOI 10.1002/(SICI)1097-4644(20000615)77:4<678::AID-JCB15>3.0.CO
  • [9] 2-P
  • [10] Integrins:: Regulators of embryogenesis
    Darribère, T
    Skalski, M
    Cousin, H
    Gaultier, A
    Montmory, C
    Alfandari, D
    [J]. BIOLOGY OF THE CELL, 2000, 92 (01) : 5 - 25