Caveolae and Bin1 form ring-shaped platforms for T-tubule initiation

• Published in: eLife 2023-04, Vol.12
• Main Authors: Lemerle, Eline, Lainé, Jeanne, Benoist, Marion, Moulay, Gilles, Bigot, Anne, Labasse, Clémence, Madelaine, Angéline, Canette, Alexis, Aubin, Perrine, Vallat, Jean-Michel, Romero, Norma B, Bitoun, Marc, Mouly, Vincent, Marty, Isabelle, Cadot, Bruno, Picas, Laura, Vassilopoulos, Stéphane
• Format: Article
• Language: English
• Subjects: Adaptor Proteins, Signal Transducing - metabolism; Analysis; Animals; Antibodies; Biosynthesis; Calcium Channels, L-Type - metabolism; Caveolae; Caveolae - metabolism; Caveolin; caveolin 3; caveolinopathies; Cell Biology; Cell Membrane - metabolism; Cell membranes; correlative microscopy; Dihydropyridine; Electron microscopes; Evolution; Excitation-contraction coupling; Gene expression; Gene silencing; Identification and classification; Life Sciences; Localization; Membrane structure; Mice; Microscopy; Muscles; Musculoskeletal system; Mutation; Neuromuscular diseases; Plasma; Properties; Proteins; Sarcoplasmic reticulum; Sarcoplasmic Reticulum - metabolism; Signal transduction; T-tubules
• ISSN: 2050-084X; 2050-084X
• DOI: 10.7554/eLife.84139

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, Bin1 and caveolae composed of caveolin-3 assemble into ring-like structures from which emerge tubes enriched in the dihydropyridine receptor. Bin1 expression 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 results in 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 dysfunction.