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Optogenetic confirmation of transverse-tubular membrane excitability in intact cardiac myocytes
M. Scardigli, M. Pásek, L. Santini, C. Palandri, E. Conti, C. Crocini, M. Campione, LM. Loew, AAF. de Vries, DA. Pijnappels, FS. Pavone, C. Poggesi, E. Cerbai, R. Coppini, P. Kohl, C. Ferrantini, L. Sacconi
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu časopisecké články
Grantová podpora
422681845
German Research Foundation
871124
European Union's Horizon 2020 research and innovation programme
NLK
Free Medical Journals
od 1878 do Před 1 rokem
PubMed Central
od 1878 do Před 1 rokem
Wiley Free Content
od 1997 do Před 1 rokem
PubMed
38348881
DOI
10.1113/jp285202
Knihovny.cz E-zdroje
- MeSH
- akční potenciály fyziologie MeSH
- buněčná membrána MeSH
- kardiomyocyty * metabolismus MeSH
- membránové potenciály MeSH
- optogenetika * MeSH
- sarkolema metabolismus MeSH
- Publikační typ
- časopisecké články MeSH
T-tubules (TT) form a complex network of sarcolemmal membrane invaginations, essential for well-co-ordinated excitation-contraction coupling (ECC) and thus homogeneous mechanical activation of cardiomyocytes. ECC is initiated by rapid depolarization of the sarcolemmal membrane. Whether TT membrane depolarization is active (local generation of action potentials; AP) or passive (following depolarization of the outer cell surface sarcolemma; SS) has not been experimentally validated in cardiomyocytes. Based on the assessment of ion flux pathways needed for AP generation, we hypothesize that TT are excitable. We therefore explored TT excitability experimentally, using an all-optical approach to stimulate and record trans-membrane potential changes in TT that were structurally disconnected, and hence electrically insulated, from the SS membrane by transient osmotic shock. Our results establish that cardiomyocyte TT can generate AP. These AP show electrical features that differ substantially from those observed in SS, consistent with differences in the density of ion channels and transporters in the two different membrane domains. We propose that TT-generated AP represent a safety mechanism for TT AP propagation and ECC, which may be particularly relevant in pathophysiological settings where morpho-functional changes reduce the electrical connectivity between SS and TT membranes. KEY POINTS: Cardiomyocytes are characterized by a complex network of membrane invaginations (the T-tubular system) that propagate action potentials to the core of the cell, causing uniform excitation-contraction coupling across the cell. In the present study, we investigated whether the T-tubular system is able to generate action potentials autonomously, rather than following depolarization of the outer cell surface sarcolemma. For this purpose, we developed a fully optical platform to probe and manipulate the electrical dynamics of subcellular membrane domains. Our findings demonstrate that T-tubules are intrinsically excitable, revealing distinct characteristics of self-generated T-tubular action potentials. This active electrical capability would protect cells from voltage drops potentially occurring within the T-tubular network.
Center for Cell Analysis and Modeling University of Connecticut Farmington CT USA
Department of Experimental and Clinical Medicine University of Florence Florence Italy
Department of Physiology Faculty of Medicine Masaryk University Brno Czech Republic
DZHK Partner Site Berlin Berlin Germany
European Laboratory for Non Linear Spectroscopy LENS Sesto Fiorentino Italy
Institute of Clinical Physiology National Research Council Florence Italy
Institute of Neuroscience and Department of Biomedical Science University of Padua Padua Italy
Institute of Thermomechanics Czech Academy of Science Prague Czech Republic
Citace poskytuje Crossref.org
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