Key result
A new endocytic capture model for T-tubule formation was proposed involving dynamic endocytic tubules, stabilization by myofibrils, and membrane delivery from the recycling endosome and Golgi.
Why the study?
The skeletal muscle T-tubule is essential for coordinated muscle contraction and shows dysmorphology in genetically inherited muscle diseases, but the mechanisms involved in its formation remained unknown due to the lack of genetically tractable systems.
Proposes a new endocytic capture model for skeletal muscle T-tubule formation using a zebrafish in vivo model.
Hypothesis-generating for T-tubule biogenesis; extends zebrafish imaging models but leaves mammalian cardiac relevance open.
The skeletal muscle T-tubule is a specialized membrane domain essential for coordinated muscle contraction that shows dysmorphology in a number of genetically inherited muscle diseases. However, in the absence of genetically tractable systems the mechanisms involved in T-tubule formation are unknown. Here, we have used the optically transparent and genetically tractable zebrafish system to probe T-tubule development in vivo . By combining live imaging with three-dimensional electron microscopy we derived a four-dimensional quantitative model for T-tubule formation. To elucidate the mechanisms involved in T-tubule formation in vivo we developed a quantitative screen for proteins that associate with and modulate early T-tubule formation including an overexpression screen of the entire zebrafish Rab protein family. We propose a new endocytic capture model involving i) formation of dynamic endocytic tubules at transient nucleation sites on the sarcolemma ii) stabilization by myofibrils/sarcoplasmic reticulum and iii) delivery of membrane from the recycling endosome and Golgi complex.
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Hall et al. (2020) studied Skeletal muscle T-tubule formation. Overexpression screen of zebrafish Rab protein family was evaluated on T-tubule formation mechanisms. A new endocytic capture model for T-tubule formation was proposed involving dynamic endocytic tubules, stabilization by myofibrils, and membrane delivery from the recycling endosome and Golgi.
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