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Visual impairment in the absence of dystroglycan.


ABSTRACT: Ocular involvement in muscular dystrophy ranges from structural defects to abnormal electroretinograms. While the mechanisms underlying the abnormal retinal physiology in patients are not understood, it is thought that alpha-dystroglycan extracellular interactions are critical for normal visual function. Here we show that beta-dystroglycan anchors dystrophin and the inward rectifying K(+) channel Kir4.1 at glial endfeet and that disruption of dystrophin and potassium channel clustering in dystroglycan mutant mice is associated with an attenuation of the electroretinogram b-wave. Glial-specific inactivation of dystroglycan or deletion of the cytoplasmic domain of beta-dystroglycan was sufficient to attenuate the electroretinogram b-wave. Unexpectedly, deletion of the beta-dystroglycan cytoplasmic domain did not disrupt the laminar structure of the retina. In contrast to the role of alpha-dystroglycan extracellular interactions during early development of the CNS, beta-dystroglycan intracellular interactions are important for visual function but not the laminar development of the retina.

SUBMITTER: Satz JS 

PROVIDER: S-EPMC2965532 | biostudies-literature | 2009 Oct

REPOSITORIES: biostudies-literature

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Visual impairment in the absence of dystroglycan.

Satz Jakob S JS   Philp Alisdair R AR   Nguyen Huy H   Kusano Hajime H   Lee Jane J   Turk Rolf R   Riker Megan J MJ   Hernández Jasmine J   Weiss Robert M RM   Anderson Michael G MG   Mullins Robert F RF   Moore Steven A SA   Stone Edwin M EM   Campbell Kevin P KP  

The Journal of neuroscience : the official journal of the Society for Neuroscience 20091001 42


Ocular involvement in muscular dystrophy ranges from structural defects to abnormal electroretinograms. While the mechanisms underlying the abnormal retinal physiology in patients are not understood, it is thought that alpha-dystroglycan extracellular interactions are critical for normal visual function. Here we show that beta-dystroglycan anchors dystrophin and the inward rectifying K(+) channel Kir4.1 at glial endfeet and that disruption of dystrophin and potassium channel clustering in dystro  ...[more]

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