Expression of intercellular adhesion molecule-1 by myofibers in mdx mice

ABSTRACT Introduction: We investigated the extent to which intercellular adhesion molecule‐1 (ICAM‐1), a critical protein of the inflammatory response, is expressed in skeletal muscles of mdx mice (a murine model of Duchenne muscular dystrophy). Methods: Muscles were collected from control and mdx m...

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Published in:Muscle & nerve Vol. 52; no. 5; pp. 795 - 802
Main Authors: Torres-Palsa, Maria J., Koziol, Matthew V., Goh, Qingnian, Cicinelli, Peter A., Peterson, Jennifer M., Pizza, Francis X.
Format: Journal Article
Language:English
Published: United States Blackwell Publishing Ltd 01-11-2015
Wiley Subscription Services, Inc
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Summary:ABSTRACT Introduction: We investigated the extent to which intercellular adhesion molecule‐1 (ICAM‐1), a critical protein of the inflammatory response, is expressed in skeletal muscles of mdx mice (a murine model of Duchenne muscular dystrophy). Methods: Muscles were collected from control and mdx mice at 2‐24 weeks of age and analyzed for ICAM‐1 expression by means of Western blot and immunofluorescence. Results: Western blot revealed higher expression of ICAM‐1 in mdx compared with control muscles through 24 weeks of age. In contrast to control muscles, ICAM‐1 was expressed on the membrane of damaged, regenerating, and normal myofibers of mdx mice. CD11b+ myeloid cells also expressed ICAM‐1 in mdx muscles, and CD11b+ cells were closely associated with the membrane of myofibers expressing ICAM‐1. Conclusions: These findings support a paradigm in which ICAM‐1 and its localization to myofibers in muscles of mdx mice contributes to the dystrophic pathology. Muscle Nerve 52: 795–802, 2015
Bibliography:National Institute of Arthritis and Musculoskeletal and Skin Diseases of the National Institutes of Health - No. R15AR064858
istex:C9538C59E81EDDD3B764D0E2C127280B85FD59B6
ark:/67375/WNG-RRQC0H3X-0
University of Toledo Interdisciplinary Research Initiation Program (FXP)
ArticleID:MUS24626
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0148-639X
1097-4598
DOI:10.1002/mus.24626