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Electrophysiological Abnormalities in VLCAD Deficient hiPSC-Cardiomyocytes Can Be Improved by Lowering Accumulation of Fatty Acid Oxidation Intermediates.
Knottnerus, Suzan J G; Mengarelli, Isabella; Wüst, Rob C I; Baartscheer, Antonius; Bleeker, Jeannette C; Coronel, Ruben; Ferdinandusse, Sacha; Guan, Kaomei; IJlst, Lodewijk; Li, Wener; Luo, Xiaojing; Portero, Vincent M; Ulbricht, Ying; Visser, Gepke; Wanders, Ronald J A; Wijburg, Frits A; Verkerk, Arie O; Houtkooper, Riekelt H; Bezzina, Connie R.
Afiliación
  • Knottnerus SJG; Laboratory Genetic Metabolic Diseases, Amsterdam UMC, University of Amsterdam, Amsterdam Gastroenterology and Metabolism, Amsterdam Cardiovascular Sciences, 1105 AZ Amsterdam, The Netherlands.
  • Mengarelli I; Department of Paediatric Metabolic Diseases, Wilhelmina Children's Hospital, University Medical Center Utrecht, 3584 EA Utrecht, The Netherlands.
  • Wüst RCI; Department of Clinical and Experimental Cardiology, Heart Center, Amsterdam Cardiovascular Sciences, Amsterdam UMC, University of Amsterdam, 1105 AZ Amsterdam, The Netherlands.
  • Baartscheer A; Laboratory Genetic Metabolic Diseases, Amsterdam UMC, University of Amsterdam, Amsterdam Gastroenterology and Metabolism, Amsterdam Cardiovascular Sciences, 1105 AZ Amsterdam, The Netherlands.
  • Bleeker JC; Department of Clinical and Experimental Cardiology, Heart Center, Amsterdam Cardiovascular Sciences, Amsterdam UMC, University of Amsterdam, 1105 AZ Amsterdam, The Netherlands.
  • Coronel R; Laboratory Genetic Metabolic Diseases, Amsterdam UMC, University of Amsterdam, Amsterdam Gastroenterology and Metabolism, Amsterdam Cardiovascular Sciences, 1105 AZ Amsterdam, The Netherlands.
  • Ferdinandusse S; Department of Paediatric Metabolic Diseases, Wilhelmina Children's Hospital, University Medical Center Utrecht, 3584 EA Utrecht, The Netherlands.
  • Guan K; Department of Clinical and Experimental Cardiology, Heart Center, Amsterdam Cardiovascular Sciences, Amsterdam UMC, University of Amsterdam, 1105 AZ Amsterdam, The Netherlands.
  • IJlst L; Laboratory Genetic Metabolic Diseases, Amsterdam UMC, University of Amsterdam, Amsterdam Gastroenterology and Metabolism, Amsterdam Cardiovascular Sciences, 1105 AZ Amsterdam, The Netherlands.
  • Li W; Institute of Pharmacology and Toxicology, Technische Universität Dresden, 01069 Dresden, Germany.
  • Luo X; Laboratory Genetic Metabolic Diseases, Amsterdam UMC, University of Amsterdam, Amsterdam Gastroenterology and Metabolism, Amsterdam Cardiovascular Sciences, 1105 AZ Amsterdam, The Netherlands.
  • Portero VM; Institute of Pharmacology and Toxicology, Technische Universität Dresden, 01069 Dresden, Germany.
  • Ulbricht Y; Institute of Pharmacology and Toxicology, Technische Universität Dresden, 01069 Dresden, Germany.
  • Visser G; Department of Clinical and Experimental Cardiology, Heart Center, Amsterdam Cardiovascular Sciences, Amsterdam UMC, University of Amsterdam, 1105 AZ Amsterdam, The Netherlands.
  • Wanders RJA; Institute of Pharmacology and Toxicology, Technische Universität Dresden, 01069 Dresden, Germany.
  • Wijburg FA; Laboratory Genetic Metabolic Diseases, Amsterdam UMC, University of Amsterdam, Amsterdam Gastroenterology and Metabolism, Amsterdam Cardiovascular Sciences, 1105 AZ Amsterdam, The Netherlands.
  • Verkerk AO; Department of Paediatric Metabolic Diseases, Wilhelmina Children's Hospital, University Medical Center Utrecht, 3584 EA Utrecht, The Netherlands.
  • Houtkooper RH; Laboratory Genetic Metabolic Diseases, Amsterdam UMC, University of Amsterdam, Amsterdam Gastroenterology and Metabolism, Amsterdam Cardiovascular Sciences, 1105 AZ Amsterdam, The Netherlands.
  • Bezzina CR; Department of Paediatric Metabolic Diseases, Emma Children's Hospital, Amsterdam UMC, University of Amsterdam, 1105 AZ Amsterdam, The Netherlands.
Int J Mol Sci ; 21(7)2020 Apr 08.
Article en En | MEDLINE | ID: mdl-32276429
Patients with very long-chain acyl-CoA dehydrogenase deficiency (VLCADD) can present with life-threatening cardiac arrhythmias. The pathophysiological mechanism is unknown. We reprogrammed fibroblasts from one mildly and one severely affected VLCADD patient, into human induced pluripotent stem cells (hiPSCs) and differentiated these into cardiomyocytes (VLCADD-CMs). VLCADD-CMs displayed shorter action potentials (APs), more delayed afterdepolarizations (DADs) and higher systolic and diastolic intracellular Ca2+ concentration ([Ca2+]i) than control CMs. The mitochondrial booster resveratrol mitigated the biochemical, electrophysiological and [Ca2+]i changes in the mild but not in the severe VLCADD-CMs. Accumulation of potentially toxic intermediates of fatty acid oxidation was blocked by substrate reduction with etomoxir. Incubation with etomoxir led to marked prolongation of AP duration and reduced DADs and [Ca2+]i in both VLCADD-CMs. These results provide compelling evidence that reduced accumulation of fatty acid oxidation intermediates, either by enhanced fatty acid oxidation flux through increased mitochondria biogenesis (resveratrol) or by inhibition of fatty acid transport into the mitochondria (etomoxir), rescues pro-arrhythmia defects in VLCADD-CMs and open doors for new treatments.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Arritmias Cardíacas / Enfermedades Mitocondriales / Miocitos Cardíacos / Acil-CoA Deshidrogenasa de Cadena Larga / Compuestos Epoxi / Ácidos Grasos / Resveratrol / Síndromes Congénitos de Insuficiencia de la Médula Ósea / Errores Innatos del Metabolismo Lipídico / Mitocondrias Tipo de estudio: Etiology_studies Límite: Humans Idioma: En Revista: Int J Mol Sci Año: 2020 Tipo del documento: Article País de afiliación: Países Bajos Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Arritmias Cardíacas / Enfermedades Mitocondriales / Miocitos Cardíacos / Acil-CoA Deshidrogenasa de Cadena Larga / Compuestos Epoxi / Ácidos Grasos / Resveratrol / Síndromes Congénitos de Insuficiencia de la Médula Ósea / Errores Innatos del Metabolismo Lipídico / Mitocondrias Tipo de estudio: Etiology_studies Límite: Humans Idioma: En Revista: Int J Mol Sci Año: 2020 Tipo del documento: Article País de afiliación: Países Bajos Pais de publicación: Suiza