Korean J Vet Res.  2013 Dec;53(4):225-230.

Alternatively activated M2 macrophages increase in early stages of experimental autoimmune myocarditis in Lewis rats

Affiliations
  • 1Laboratory of Veterinary Anatomy, College of Veterinary Medicine and Veterinary Medical Research Institute, Jeju National University, Jeju 690-756, Korea. shint@jejunu.ac.kr
  • 2School of Medicine, Jeju National University, Jeju 690-756, Korea.
  • 3Department of Immunotherapy Development, Tokyo Metropolitan Institute of Medical Science, Tokyo 156-8506, Japan.

Abstract

To better understand the role of macrophages in early stages of experimental autoimmune myocarditis (EAM), we compared the expression of inducible nitric oxide synthase (iNOS) and arginase-1, markers for classically activated M1 and alternatively activated M2 macrophages, respectively, in the hearts of EAM-affected and control rats. Immunohistochemical evidence revealed that both iNOS-positive and arginase 1-positive macrophages were found in EAM lesions, while some cells were co-localized with both markers. This finding suggests that the increased level of arginase-1, which is partly from M2 macrophages, contributes to the modulation of EAM, possibly through the reduction of nitric oxide in the lesion.

Keyword

arginase-1; experimental autoimmune myocarditis; inducible nitric oxide synthase; macrophage

MeSH Terms

Animals
Arginase
Heart
Macrophages*
Myocarditis*
Nitric Oxide
Nitric Oxide Synthase Type II
Rats*
Arginase
Nitric Oxide
Nitric Oxide Synthase Type II
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