Link to bioRxiv paper:
http://biorxiv.org/cgi/content/short/2022.11.01.514746v1?rss=1

Authors: Lemerle, E., Laine, J., Moulay, G., Bigot, A., Labasse, C., Madelaine, A., Canette, A., Aubin, P., Vallat, J.-M., Romero, N. B., Bitoun, M., Mouly, V., Isabelle, M., Cadot, B., Picas, L., Vassilopoulos, S.

Abstract:
Excitation-contraction coupling requires a highly specialized membrane structure, the triad, composed of a plasma membrane invagination, the T-tubule, surrounded by two sarcoplasmic reticulum terminal cisternae. Although the precise mechanisms governing T-tubule biogenesis and triad formation remain largely unknown, studies have shown that caveolae participate in T-tubule formation and mutations of several of their constituents induce muscle weakness and myopathies. Here, we demonstrate that, at the plasma membrane, caveolae composed of caveolin-3 and Bin1 assemble into ring-like structures from which emerge tubes enriched in the dihydropyridine receptor. Overexpression of Bin1 lead to the formation of both rings and tubes and we show that Bin1 forms scaffolds on which caveolae accumulate to form the initial T-tubule. Cav3 deficiency caused by either gene silencing or pathogenic mutations cause defective ring formation and perturbed Bin1-mediated tubulation that may explain defective T-tubule organization in mature muscles. Our results uncover new pathophysiological mechanisms that may prove relevant to myopathies caused by Cav3 or Bin1.

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