Published online before print October 2, 2008

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Copyright © 2008 American Society for Investigative Pathology
American Journal of Pathology, doi:10.2353/ajpath.2008.080098

Accepted for publication July 29, 2008.

Article

Dysferlin Deficiency Shows Compensatory Induction of Rab27A/Slp2a that May Contribute to Inflammatory Onset

Akanchha Kesari^*, Mitsunori Fukuda, Susan Knoblach^*, Rumaisa Bashir, Gustavo A. Nader^*, Deepak Rao^*, Kanneboyina Nagaraju^*, and Eric P. Hoffman^*@

From the Research Center for Genetic Medicine,* Children's National Medical Center, Washington DC; Department of Developmental Biology and Neurosciences, Tohoku University, Miyagi, Japan; and School of Biological and Biochemical Sciences, University of Durham, Durham, United Kingdom

^@ To whom correspondence should be addressed. E-mail: ehoffman{at}cnmcresearch.org.

	Abstract

Mutations in the dysferlin gene cause limb girdle muscular dystrophy 2B (LGMD2B) and Miyoshi myopathy. Dysferlin-deficient cells show abnormalities in vesicular traffic and membrane repair although onset of symptoms is not commonly seen until the late teenage years and is often associated with subacute onset and marked muscle inflammation. To identify molecular networks specific to dysferlin-deficient muscle that might explain disease pathogenesis, muscle mRNA profiles from 10 mutation-positive LGMD2B/MM patients were compared with a disease control [LGMD2I; (n = 9)], and normal muscle samples (n = 11). Query of inflammatory pathways suggested LGMD2B-specific increases in co-stimulatory signaling between dendritic cells and T cells (CD86, CD28, and CTLA4), associated with localized expression of both versican and tenascin. LGMD2B muscle also showed an increase in vesicular trafficking pathway proteins not normally observed in muscle (synaptotagmin-like protein Slp2a/SYTL2 and the small GTPase Rab27A). We propose that Rab27A/Slp2a expression in LGMD2B muscle provides a compensatory vesicular trafficking pathway that is able to repair membrane damage in the absence of dysferlin. However, this same pathway may release endocytotic vesicle contents, resulting in an inflammatory microenvironment. As dysferlin deficiency has been shown to enhance phagocytosis by macrophages, together with our findings of abnormal myofiber endocytosis pathways and dendritic-T cell activation markers, these results suggest a model of immune and inflammatory network over-stimulation that may explain the subacute inflammatory presentation.

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