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Updated: Aug 8, 2026

Modeling Myotonic Dystrophy 1 in C2C12 Myoblast Cells
Published on: July 29, 2016
SERCA1 and calsequestrin storage myopathy: a new surplus protein myopathy
Giuliano Tomelleri1, Laura Palmucci, Paola Tonin
1Department of Neurological Sciences and Vision, Section of Clinical Neurology, University of Verona, Verona, Italy. giuliano.tomelleri@univr.it
Abstract:
We describe four patients, from four different families, affected by a mild myopathy or asymptomatic elevated serum creatine kinase levels, in whom toluidine blue-stained semithin sections of muscle specimens revealed inclusions of different size and shape. The inclusions did not stain by routine histochemical studies. The sarcoplasmic or endoplasmic reticulum calcium 1 (SERCA1) ATPase and/or calsequestrin reactivity of inclusions, by immunohistochemistry, and the SERCA1- and calsequestrin-increased expression, by immunoblot, suggested that inclusions were constituted by an excess of proteins normally present in the terminal cisternae of sarcoplasmic reticulum. Our cases, both sporadic and familial, represent a new type of surplus protein myopathy.
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