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Axial Tubule Junctions Activate Atrial Ca2+ Release Across Species

  Articoli su Riviste JCR/ISI  (anno 2018)

Autori:  Brandenburg S., Pawlowitz J., Fakuade F.E., Kownatzki-Danger D., Kohl T., Mitronova G.Y., Scardigli M., Neef J., Schmidt C., Wiedmann F., Pavone F.S., Sacconi L., Kutschka I., Sossalla S., Moser T., Voigt N., Lehnart S

Affiliazione Autori:  Heart Research Center Göttingen, Department of Cardiology and Pneumology, University Medical Center Göttingen, Göttingen, Germany; Heart Research Center Göttingen, Institute of Pharmacology and Toxicology, University Medical Center Göttingen, Göttingen, Germany; Department of NanoBiophotonics, Max Planck Institute for Biophysical Chemistry, Göttingen, Germany; European Laboratory for Non-Linear Spectroscopy and National Institute of Optics (INO-CNR), Sesto Fiorentino, Italy; Institute for Auditory Neuroscience and InnerEarLab, University Medical Center Göttingen, Göttingen, Germany; DZHK (German Centre for Cardiovascular Research) partner site Heidelberg/Mannheim, University of Heidelberg, Heidelberg, Germany; Heidelberg Center for Heart Rhythm Disorders, University Hospital Heidelberg, Heidelberg, Germany; Department of Cardiology, University Hospital Heidelberg, Heidelberg, Germany; Department of Physics, University of Florence, Florence, Italy; Department of Cardiothoracic and Vascular Surgery, University Medical Center Göttingen, Göttingen, Germany; DZHK (German Centre for Cardiovascular Research) partner site Göttingen, Göttingen, Germany; BioMET, The Center for Biomedical Engineering and Technology, University of Maryland School of Medicine, Baltimore, MD, United States

Riassunto:  Rationale: Recently, abundant axial tubule (AT) membrane structures were identified deep inside atrial myocytes (AMs). Upon excitation, ATs rapidly activate intracellular Ca2+ release and sarcomeric contraction through extensive AT junctions, a cell-specific atrial mechanism. While AT junctions with the sarcoplasmic reticulum contain unusually large clusters of ryanodine receptor 2 (RyR2) Ca2+ release channels in mouse AMs, it remains unclear if similar protein networks and membrane structures exist across species, particularly those relevant for atrial disease modeling. Objective: To examine and quantitatively analyze the architecture of AT membrane structures and associated Ca2+ signaling proteins across species from mouse to human. Methods and Results: We developed superresolution microscopy (nanoscopy) strategies for intact live AMs based on a new custom-made photostable cholesterol dye and immunofluorescence imaging of membraneous structures and membrane proteins in fixed tissue sections from human, porcine, and rodent atria. Consistently, in mouse, rat, and rabbit AMs, intact cell-wide tubule networks continuous with the surface membrane were observed, mainly composed of ATs. Moreover, co-immunofluorescence nanoscopy showed L-type Ca2+ channel clusters adjacent to extensive junctional RyR2 clusters at ATs. However, only junctional RyR2 clusters were highly phosphorylated and may thus prime Ca2+ release at ATs, locally for rapid signal amplification. While the density of the integrated L-type Ca2+ current was similar in human and mouse AMs, the intracellular Ca2+ transient showed quantitative differences. Importantly, local intracellular Ca2+ release from AT junctions occurred through instantaneous action potential propagation via transverse tubules (TTs) from the surface membrane. Hence, sparse TTs were sufficient as electrical conduits for rapid activation of Ca2+ release through ATs. Nanoscopy of atrial tissue sections confirmed abundant ATs as the major network component of AMs, particularly in human atrial tissue sections. Conclusion: AT junctions represent a conserved, cell-specific membrane structure for rapid excitation-contraction coupling throughout a representative spectrum of species including human. Since ATs provide the major excitable membrane network component in AMs, a new model of atrial "super-hub" Ca2+ signaling may apply across biomedically relevant species, opening avenues for future investigations about atrial disease mechanisms and therapeutic targeting.

Volume n.:  9      Pagine da: 01227-1  a: 01227-21
DOI: 10.3389/fphys.2018.01227

   *Citazioni: 3
data tratti da "WEB OF SCIENCE" (marchio registrato di Thomson Reuters) ed aggiornati a:  19/05/2019

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