Literature DB >> 9882504

Expression of matrix metalloproteinases 2 and 9 in regenerating skeletal muscle: a study in experimentally injured and mdx muscles.

S Kherif1, C Lafuma, M Dehaupas, S Lachkar, J G Fournier, M Verdière-Sahuqué, M Fardeau, H S Alameddine.   

Abstract

Matrix metalloproteinases (MMPs) cooperatively degrade all components of the extracellular matrix (ECM). Remodeling of ECM during skeletal muscle degeneration and regeneration suggests a tight regulation of matrix-degrading activity during muscle regeneration. In this study, we investigated the expression of MMP-2 and MMP-9, in normal muscles and their regulation during regeneration process. We further investigated their secretion by C2C12 myogenic cell line. Two models of muscle degeneration-regeneration were used: (1) normal muscles in which necrosis was experimentally induced by cardiotoxin injection; (2) mdx muscles which exhibit recurrent signs of focal myofiber necrosis followed by successful regeneration. MMPs were studied by zymography; their free activity was quantified using 3H-labeled gelatin substrate and mRNA expression was followed by Northern hybridization. Muscle degeneration-regeneration was analyzed by conventional morphological methods and in situ hybridization was performed on muscle sections to identify the cells expressing these MMPs. Results show that MMP-2, but not MMP-9 expression, is constitutive in normal muscles. Upon injury, the active form of MMP-2 is transiently increased, whereas MMP-9 is induced within 24 h and remains present for several days. Quantitative assays of free gelatinolytic activity show a progressive and steady increase that culminates at 7 days postinjury and slowly returns to normal levels. In adult mdx mice, both pro and active forms of MMP-2 and MMP-9 are expressed. Northern blot results support these findings. Zymography of C2C12-conditioned medium shows that myogenic cells produce MMP-2. By in situ hybridization we localized MMP-9 mRNA in inflammatory cells and putative activated satellite cells in injured muscles. Our data allow the correlation of the differential expression of pro and/or active forms of MMP-2 and MMP-9 with different stages of the degeneration-regeneration process: MMP-9 expression is related to the inflammatory response and probably to the activation of satellite cells, whereas MMP-2 activation is concomitant with the regeneration of new myofibers. Copyright 1999 Academic Press.

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Year:  1999        PMID: 9882504     DOI: 10.1006/dbio.1998.9107

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  91 in total

1.  Regulation of TIMP-2, MT1-MMP, and MMP-2 expression during C2C12 differentiation.

Authors:  Gentian Lluri; Diane M Jaworski
Journal:  Muscle Nerve       Date:  2005-10       Impact factor: 3.217

2.  Effect of beta-dystroglycan processing on utrophin/Dp116 anchorage in normal and mdx mouse Schwann cell membrane.

Authors:  K Hnia; G Hugon; A Masmoudi; J Mercier; F Rivier; D Mornet
Journal:  Neuroscience       Date:  2006-06-02       Impact factor: 3.590

3.  LLLT actives MMP-2 and increases muscle mechanical resistance after nerve sciatic rat regeneration.

Authors:  Rodrigo Antonio Carvalho Andraus; Luciana Prado Maia; Anderson Diogo de Souza Lino; Karen Barron Parron Fernandes; Marcos Vinícius de Matos Gomes; Rinaldo Roberto de Jesus Guirro; Cláudio Henrique Barbieri
Journal:  Lasers Med Sci       Date:  2017-03-06       Impact factor: 3.161

4.  Modulation of p38 mitogen-activated protein kinase cascade and metalloproteinase activity in diaphragm muscle in response to free radical scavenger administration in dystrophin-deficient Mdx mice.

Authors:  Karim Hnia; Gerald Hugon; François Rivier; Ahmed Masmoudi; Jacques Mercier; Dominique Mornet
Journal:  Am J Pathol       Date:  2007-02       Impact factor: 4.307

5.  Muscle CD31(-) CD45(-) side population cells promote muscle regeneration by stimulating proliferation and migration of myoblasts.

Authors:  Norio Motohashi; Akiyoshi Uezumi; Erica Yada; So-ichiro Fukada; Kazuhiro Fukushima; Kazuhiko Imaizumi; Yuko Miyagoe-Suzuki; Shin'ichi Takeda
Journal:  Am J Pathol       Date:  2008-07-31       Impact factor: 4.307

6.  Osteopontin-stimulated expression of matrix metalloproteinase-9 causes cardiomyopathy in the mdx model of Duchenne muscular dystrophy.

Authors:  Saurabh Dahiya; Srikanth Givvimani; Shephali Bhatnagar; Natia Qipshidze; Suresh C Tyagi; Ashok Kumar
Journal:  J Immunol       Date:  2011-08-01       Impact factor: 5.422

Review 7.  Role of matrix metalloproteinases in skeletal muscle: migration, differentiation, regeneration and fibrosis.

Authors:  Xiaoping Chen; Yong Li
Journal:  Cell Adh Migr       Date:  2009-10-24       Impact factor: 3.405

8.  Slow-adhering stem cells derived from injured skeletal muscle have improved regenerative capacity.

Authors:  Xiaodong Mu; Guosheng Xiang; Christopher R Rathbone; Haiying Pan; Ian H Bellayr; Thomas J Walters; Yong Li
Journal:  Am J Pathol       Date:  2011-06-02       Impact factor: 4.307

9.  Regulation of type IV collagen gene expression and degradation in fast and slow muscles during dexamethasone treatment and exercise.

Authors:  A M Ahtikoski; E-M Riso; S O A Koskinen; J Risteli; T E S Takala
Journal:  Pflugers Arch       Date:  2003-12-18       Impact factor: 3.657

10.  Sca-1 expression is required for efficient remodeling of the extracellular matrix during skeletal muscle regeneration.

Authors:  Kimberly A Kafadar; Lin Yi; Yusra Ahmad; Leslie So; Fabio Rossi; Grace K Pavlath
Journal:  Dev Biol       Date:  2008-11-06       Impact factor: 3.582

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