Literature DB >> 15637171

Inflammatory processes in muscle injury and repair.

James G Tidball1.   

Abstract

Modified muscle use or injury can produce a stereotypic inflammatory response in which neutrophils rapidly invade, followed by macrophages. This inflammatory response coincides with muscle repair, regeneration, and growth, which involve activation and proliferation of satellite cells, followed by their terminal differentiation. Recent investigations have begun to explore the relationship between inflammatory cell functions and skeletal muscle injury and repair by using genetically modified animal models, antibody depletions of specific inflammatory cell populations, or expression profiling of inflamed muscle after injury. These studies have contributed to a complex picture in which inflammatory cells promote both injury and repair, through the combined actions of free radicals, growth factors, and chemokines. In this review, recent discoveries concerning the interactions between skeletal muscle and inflammatory cells are presented. New findings clearly show a role for neutrophils in promoting muscle damage soon after muscle injury or modified use. No direct evidence is yet available to show that neutrophils play a beneficial role in muscle repair or regeneration. Macrophages have also been shown capable of promoting muscle damage in vivo and in vitro through the release of free radicals, although other findings indicate that they may also play a role in muscle repair and regeneration through growth factors and cytokine-mediated signaling. However, this role for macrophages in muscle regeneration is still not definitive; other cells present in muscle can also produce the potentially regenerative factors, and it remains to be proven whether macrophage-derived factors are essential for muscle repair or regeneration in vivo. New evidence also shows that muscle cells can release positive and negative regulators of inflammatory cell invasion, and thereby play an active role in modulating the inflammatory process. In particular, muscle-derived nitric oxide can inhibit inflammatory cell invasion of healthy muscle and protect muscle from lysis by inflammatory cells in vivo and in vitro. On the other hand, muscle-derived cytokines can signal for inflammatory cell invasion, at least in vitro. The immediate challenge for advancing our current understanding of the relationships between muscle and inflammatory cells during muscle injury and repair is to place what has been learned in vitro into the complex and dynamic in vivo environment.

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Year:  2005        PMID: 15637171     DOI: 10.1152/ajpregu.00454.2004

Source DB:  PubMed          Journal:  Am J Physiol Regul Integr Comp Physiol        ISSN: 0363-6119            Impact factor:   3.619


  413 in total

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Journal:  Mol Ther       Date:  2011-09-20       Impact factor: 11.454

4.  Muscle satellite cells from GRMD dystrophic dogs are not phenotypically distinguishable from wild type satellite cells in ex vivo culture.

Authors:  Zachary Berg; Lucas R Beffa; Daniel P Cook; D D W Cornelison
Journal:  Neuromuscul Disord       Date:  2011-01-28       Impact factor: 4.296

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6.  Unloading stress disturbs muscle regeneration through perturbed recruitment and function of macrophages.

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Journal:  J Appl Physiol (1985)       Date:  2012-03-01

7.  Chemokine expression and control of muscle cell migration during myogenesis.

Authors:  Christine A Griffin; Luciano H Apponi; Kimberly K Long; Grace K Pavlath
Journal:  J Cell Sci       Date:  2010-08-24       Impact factor: 5.285

8.  Maternal obesity downregulates myogenesis and beta-catenin signaling in fetal skeletal muscle.

Authors:  Jun F Tong; Xu Yan; Mei J Zhu; Stephen P Ford; Peter W Nathanielsz; Min Du
Journal:  Am J Physiol Endocrinol Metab       Date:  2009-01-27       Impact factor: 4.310

9.  Massage therapy restores peripheral vascular function after exertion.

Authors:  Nina C Franklin; Mohamed M Ali; Austin T Robinson; Edita Norkeviciute; Shane A Phillips
Journal:  Arch Phys Med Rehabil       Date:  2014-02-25       Impact factor: 3.966

10.  Altered macrophage phenotype transition impairs skeletal muscle regeneration.

Authors:  Hanzhou Wang; David W Melton; Laurel Porter; Zaheer U Sarwar; Linda M McManus; Paula K Shireman
Journal:  Am J Pathol       Date:  2014-02-11       Impact factor: 4.307

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