Anti-inflammatory macrophages improve skeletal muscle recovery from ischemia-reperfusion
Author(s) -
David W. Hammers,
Viktoriya Rybalko,
Melissa MerschamBanda,
PeiLing Hsieh,
Laura J. Suggs,
Roger P. Farrar
Publication year - 2015
Publication title -
journal of applied physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.253
H-Index - 229
eISSN - 8750-7587
pISSN - 1522-1601
DOI - 10.1152/japplphysiol.00313.2014
Subject(s) - skeletal muscle , integrin alpha m , flow cytometry , inflammation , reperfusion injury , ischemia , downregulation and upregulation , regeneration (biology) , innate immune system , immune system , biology , immunology , medicine , microbiology and biotechnology , biochemistry , gene
The presence of macrophages (MPs) is essential for skeletal muscle to properly regenerate following injury. The aim of this study was the evaluation of MP profiles and their importance in skeletal muscle recovering from tourniquet-induced ischemia-reperfusion (I/R). Using flow cytometry, we identified two distinct CD11b(+) MP populations that differ in expression of the surface markers Ly-6C and F4/80. These populations are prominent at 3 and 5 days of reperfusion and molecularly correspond to inflammatory and anti-inflammatory MP phenotypes. Sorted MP populations demonstrated high levels of IGF-I expression, and whole muscle post-I/R IGF-I expression strongly correlates with F4/80 expression. This suggests MPs largely influence postinjury IGF-I upregulation. We additionally demonstrate that direct intramuscular injection of FACS-isolated CD11b(+)Ly-6C(lo)F4/80(hi) MPs improves the functional and histological recovery of I/R-affected muscle. Taken together, these data further support the substantial influence of the innate immune system on muscle regeneration and suggest MP-focused therapeutic approaches may greatly facilitate skeletal muscle recovery from substantial injury.
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