| Literature DB >> 17108690 |
Hiroshi Nemoto1, Shingo Konno, Hiroshi Nakazora, Hiroko Miura, Teruyuki Kurihara.
Abstract
SJL/J mice have been studied as the model animals for autoimmunological diseases. Recently it was clarified that SJL/J mice have a defect of dysferlin. Human limb girdle muscular dystrophy 2B and Miyoshi myopathy also have a defect of dysferlin. In this study we present the histological and immunohistological changes in the natural course. Histological study revealed that SJL/J mice had inflammatory, degenerative changes, and neurogenic changes in later ages. As for interstitial inflammatory cells, the macrophages were dominant in any age, and in the T cell subset, the CD4+ T cells were more abundant than the CD8+ T cells, and few B cells were seen. The laboratory data showed a high level of creatine kinase in all ages. It is suspected that the inflammatory changes were induced by the primary immunological abnormality or by the defect of dysferlin in SJL/J mice. Copyright 2007 S. Karger AG, Basel.Entities:
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Year: 2006 PMID: 17108690 DOI: 10.1159/000097005
Source DB: PubMed Journal: Eur Neurol ISSN: 0014-3022 Impact factor: 1.710