Your browser doesn't support javascript.
loading
Optical Interrogation of Sympathetic Neuronal Effects on Macroscopic Cardiomyocyte Network Dynamics.
Burton, Rebecca-Ann B; Tomek, Jakub; Ambrosi, Christina M; Larsen, Hege E; Sharkey, Amy R; Capel, Rebecca A; Corbett, Alexander D; Bilton, Samuel; Klimas, Aleksandra; Stephens, Guy; Cremer, Maegan; Bose, Samuel J; Li, Dan; Gallone, Giuseppe; Herring, Neil; Mann, Edward O; Kumar, Abhinav; Kramer, Holger; Entcheva, Emilia; Paterson, David J; Bub, Gil.
Afiliación
  • Burton RB; University of Oxford, Department of Pharmacology, Mansfield Road, Oxford OX1 3QT, UK; University of Oxford, Department of Physiology, Anatomy and Genetics, British Heart Foundation Centre of Research Excellence, Parks Road, Oxford OX1 3PT, UK. Electronic address: rebecca.burton@pharm.ox.ac.uk.
  • Tomek J; University of Oxford, Department of Physiology, Anatomy and Genetics, British Heart Foundation Centre of Research Excellence, Parks Road, Oxford OX1 3PT, UK.
  • Ambrosi CM; The George Washington University, Department of Biomedical Engineering, Washington, DC 20052, USA.
  • Larsen HE; University of Oxford, Department of Physiology, Anatomy and Genetics, British Heart Foundation Centre of Research Excellence, Parks Road, Oxford OX1 3PT, UK.
  • Sharkey AR; University of Oxford, Department of Physiology, Anatomy and Genetics, British Heart Foundation Centre of Research Excellence, Parks Road, Oxford OX1 3PT, UK.
  • Capel RA; University of Oxford, Department of Pharmacology, Mansfield Road, Oxford OX1 3QT, UK.
  • Corbett AD; University of Exeter, Physics and Astronomy, Exeter EX4 4QL, UK.
  • Bilton S; University of Oxford, Department of Physiology, Anatomy and Genetics, British Heart Foundation Centre of Research Excellence, Parks Road, Oxford OX1 3PT, UK.
  • Klimas A; The George Washington University, Department of Biomedical Engineering, Washington, DC 20052, USA.
  • Stephens G; University of Oxford, Department of Physiology, Anatomy and Genetics, British Heart Foundation Centre of Research Excellence, Parks Road, Oxford OX1 3PT, UK.
  • Cremer M; University of Oxford, Department of Pharmacology, Mansfield Road, Oxford OX1 3QT, UK.
  • Bose SJ; University of Oxford, Department of Pharmacology, Mansfield Road, Oxford OX1 3QT, UK.
  • Li D; University of Oxford, Department of Physiology, Anatomy and Genetics, British Heart Foundation Centre of Research Excellence, Parks Road, Oxford OX1 3PT, UK.
  • Gallone G; University of Oxford, Department of Physiology, Anatomy and Genetics, British Heart Foundation Centre of Research Excellence, Parks Road, Oxford OX1 3PT, UK; Department of Computational Molecular Biology, Max Planck Institute for Molecular Genetics, Ihnestraße 63-73, 14195 Berlin, Germany.
  • Herring N; University of Oxford, Department of Physiology, Anatomy and Genetics, British Heart Foundation Centre of Research Excellence, Parks Road, Oxford OX1 3PT, UK.
  • Mann EO; University of Oxford, Department of Physiology, Anatomy and Genetics, British Heart Foundation Centre of Research Excellence, Parks Road, Oxford OX1 3PT, UK.
  • Kumar A; University of Oxford, Department of Biochemistry, Glycobiology Institute, Oxford, UK.
  • Kramer H; University of Oxford, Department of Physiology, Anatomy and Genetics, British Heart Foundation Centre of Research Excellence, Parks Road, Oxford OX1 3PT, UK.
  • Entcheva E; The George Washington University, Department of Biomedical Engineering, Washington, DC 20052, USA.
  • Paterson DJ; University of Oxford, Department of Physiology, Anatomy and Genetics, British Heart Foundation Centre of Research Excellence, Parks Road, Oxford OX1 3PT, UK.
  • Bub G; University of Oxford, Department of Physiology, Anatomy and Genetics, British Heart Foundation Centre of Research Excellence, Parks Road, Oxford OX1 3PT, UK; McGill University, Department of Physiology, McIntyre Medical Sciences Building, Room 1128, 3655 Promenade Sir William Osler, Montréal, QC H3G
iScience ; 23(7): 101334, 2020 Jul 24.
Article en En | MEDLINE | ID: mdl-32674058
ABSTRACT
Cardiac stimulation via sympathetic neurons can potentially trigger arrhythmias. We present approaches to study neuron-cardiomyocyte interactions involving optogenetic selective probing and all-optical electrophysiology to measure activity in an automated fashion. Here we demonstrate the utility of optical interrogation of sympathetic neurons and their effects on macroscopic cardiomyocyte network dynamics to address research targets such as the effects of adrenergic stimulation via the release of neurotransmitters, the effect of neuronal numbers on cardiac behavior, and the applicability of optogenetics in mechanistic in vitro studies. As arrhythmias are emergent behaviors that involve the coordinated activity of millions of cells, we image at macroscopic scales to capture complex dynamics. We show that neurons can both decrease and increase wave stability and re-entrant activity in culture depending on their induced activity-a finding that may help us understand the often conflicting results seen in experimental and clinical studies.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: IScience Año: 2020 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: IScience Año: 2020 Tipo del documento: Article