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J Biol Chem, Vol. 274, Issue 12, 8240-8246, March 19, 1999

Characterization of the Transmembrane Molecular Architecture of the Dystroglycan Complex in Schwann Cells

Fumiaki SaitoDagger , Toshihiro Masaki§, Keiko Kamakura§, Louise V. B. Anderson, Sachiko FujitaDagger , Hiroko Fukuta-OhiDagger , Yoshihide SunadaDagger , Teruo ShimizuDagger , and Kiichiro MatsumuraDagger

From the Dagger  Department of Neurology and Neuroscience, Teikyo University School of Medicine, Tokyo 173-8605, Japan, the § Third Department of Internal Medicine, National Defense Medical College, Saitama 359-8513, Japan, and the  University School of Neuroscience and Muscular Dystrophy Group Laboratories, Regional Neuroscience Centre, Newcastle General Hospital, Newcastle-upon-Tyne NE4 6BE, United Kingdom

We have demonstrated previously 1) that the dystroglycan complex, but not the sarcoglycan complex, is expressed in peripheral nerve, and 2) that alpha -dystroglycan is an extracellular laminin-2-binding protein anchored to beta -dystroglycan in the Schwann cell membrane. In the present study, we investigated the transmembrane molecular architecture of the dystroglycan complex in Schwann cells. The cytoplasmic domain of beta -dystroglycan was co-localized with Dp116, the Schwann cell-specific isoform of dystrophin, in the abaxonal Schwann cell cytoplasm adjacent to the outer membrane. beta -dystroglycan bound to Dp116 mainly via the 15 C-terminal amino acids of its cytoplasmic domain, but these amino acids were not solely responsible for the interaction of these two proteins. Interestingly, the beta -dystroglycan-precipitating antibody precipitated only a small fraction of alpha -dystroglycan and did not precipitate laminin and Dp116 from the peripheral nerve extracts. Our results indicate 1) that Dp116 is a component of the submembranous cytoskeletal system that anchors the dystroglycan complex in Schwann cells, and 2) that the dystroglycan complex in Schwann cells is fragile compared with that in striated muscle cells. We propose that this fragility may be attributable to the absence of the sarcoglycan complex in Schwann cells.


Copyright © 1999 by The American Society for Biochemistry and Molecular Biology, Inc.

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