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Macrophage Plasticity in Skeletal Muscle Repair
Author(s) -
Elena Rigamonti,
Paola Zordan,
Clara Sciorati,
Patrizia RovereQuerini,
Silvia Brunelli
Publication year - 2014
Publication title -
biomed research international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.772
H-Index - 126
eISSN - 2314-6141
pISSN - 2314-6133
DOI - 10.1155/2014/560629
Subject(s) - macrophage , macrophage polarization , proinflammatory cytokine , phenotype , biology , skeletal muscle , immunology , m2 macrophage , inflammation , innate immune system , fibrosis , microbiology and biotechnology , regeneration (biology) , pathology , immune system , medicine , anatomy , in vitro , genetics , gene
Macrophages are one of the first barriers of host defence against pathogens. Beyond their role in innate immunity, macrophages play increasingly defined roles in orchestrating the healing of various injured tissues. Perturbations of macrophage function and/or activation may result in impaired regeneration and fibrosis deposition as described in several chronic pathological diseases. Heterogeneity and plasticity have been demonstrated to be hallmarks of macrophages. In response to environmental cues they display a proinflammatory (M1) or an alternative anti-inflammatory (M2) phenotype. A lot of evidence demonstrated that after acute injury M1 macrophages infiltrate early to promote the clearance of necrotic debris, whereas M2 macrophages appear later to sustain tissue healing. Whether the sequential presence of two different macrophage populations results from a dynamic shift in macrophage polarization or from the recruitment of new circulating monocytes is a subject of ongoing debate. In this paper, we discuss the current available information about the role that different phenotypes of macrophages plays after injury and during the remodelling phase in different tissue types, with particular attention to the skeletal muscle.

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