Literature DB >> 28082092

Energy utilization of induced pluripotent stem cell-derived cardiomyocyte in Fabry disease.

Shih-Jie Chou1, Wen-Chung Yu2, Yuh-Lih Chang3, Wen-Yeh Chen4, Wei-Chao Chang5, Yueh Chien6, Jiin-Cherng Yen7, Yung-Yang Liu8, Shih-Jen Chen6, Chien-Ying Wang9, Yu-Han Chen10, Dau-Ming Niu11, Shing-Jong Lin12, Jaw-Wen Chen13, Shih-Hwa Chiou14, Hsin-Bang Leu15.   

Abstract

BACKGROUND: Fabry disease (FD) is a lysosomal storage disease in which glycosphingolipids (GB3) accumulate in organs of the human body, leading to idiopathic hypertrophic cardiomyopathy and target organ damage. Its pathophysiology is still poorly understood.
OBJECTIVES: We aimed to generate patient-specific induced pluripotent stem cells (iPSC) from FD patients presenting cardiomyopathy to determine whether the model could recapitulate key features of the disease phenotype and to investigate the energy metabolism in Fabry disease.
METHODS: Peripheral blood mononuclear cells from a 30-year-old Chinese man with a diagnosis of Fabry disease, GLA gene (IVS4+919G>A) mutation were reprogrammed into iPSCs and differentiated into iPSC-CMs and energy metabolism was analyzed in iPSC-CMs.
RESULTS: The FD-iPSC-CMs recapitulated numerous aspects of the FD phenotype including reduced GLA activity, cellular hypertrophy, GB3 accumulation and impaired contractility. Decreased energy metabolism with energy utilization shift to glycolysis was observed, but the decreased energy metabolism was not modified by enzyme rescue replacement (ERT) in FD-iPSCs-CMs.
CONCLUSION: This model provided a promising in vitro model for the investigation of the underlying disease mechanism and development of novel therapeutic strategies for FD. This potential remedy for enhancing the energetic network and utility efficiency warrants further study to identify novel therapies for the disease. Copyright Â
© 2017 Elsevier B.V. All rights reserved.

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Year:  2017        PMID: 28082092     DOI: 10.1016/j.ijcard.2017.01.009

Source DB:  PubMed          Journal:  Int J Cardiol        ISSN: 0167-5273            Impact factor:   4.164


  17 in total

1.  Fabry Disease: A New Model of Premature Ageing?

Authors:  Jeroen P Kooman; Peter Stenvinkel; Paul G Shiels
Journal:  Nephron       Date:  2019-09-27       Impact factor: 2.847

Review 2.  Modelling inherited cardiac disease using human induced pluripotent stem cell-derived cardiomyocytes: progress, pitfalls, and potential.

Authors:  Alain van Mil; Geerthe Margriet Balk; Klaus Neef; Jan Willem Buikema; Folkert W Asselbergs; Sean M Wu; Pieter A Doevendans; Joost P G Sluijter
Journal:  Cardiovasc Res       Date:  2018-12-01       Impact factor: 10.787

Review 3.  Ion channels and pain in Fabry disease.

Authors:  Carina Weissmann; Adriana A Albanese; Natalia E Contreras; María N Gobetto; Libia C Salinas Castellanos; Osvaldo D Uchitel
Journal:  Mol Pain       Date:  2021 Jan-Dec       Impact factor: 3.395

Review 4.  Human heart disease: lessons from human pluripotent stem cell-derived cardiomyocytes.

Authors:  E Giacomelli; C L Mummery; M Bellin
Journal:  Cell Mol Life Sci       Date:  2017-06-01       Impact factor: 9.261

Review 5.  Induced pluripotent stem cell models of lysosomal storage disorders.

Authors:  Daniel K Borger; Benjamin McMahon; Tamanna Roshan Lal; Jenny Serra-Vinardell; Elma Aflaki; Ellen Sidransky
Journal:  Dis Model Mech       Date:  2017-06-01       Impact factor: 5.758

Review 6.  Investigating pediatric disorders with induced pluripotent stem cells.

Authors:  Matthew D Durbin; Adrian G Cadar; Young Wook Chun; Charles C Hong
Journal:  Pediatr Res       Date:  2018-05-30       Impact factor: 3.756

7.  Cardiomyopathy phenotypes in human-induced pluripotent stem cell-derived cardiomyocytes-a systematic review.

Authors:  Thomas Eschenhagen; Lucie Carrier
Journal:  Pflugers Arch       Date:  2018-10-15       Impact factor: 3.657

Review 8.  Human Induced Pluripotent Stem-Cell-Derived Cardiomyocytes as Models for Genetic Cardiomyopathies.

Authors:  Andreas Brodehl; Hans Ebbinghaus; Marcus-André Deutsch; Jan Gummert; Anna Gärtner; Sandra Ratnavadivel; Hendrik Milting
Journal:  Int J Mol Sci       Date:  2019-09-06       Impact factor: 5.923

9.  Inhibition of Arachidonate 12/15-Lipoxygenase Improves α-Galactosidase Efficacy in iPSC-Derived Cardiomyocytes from Fabry Patients.

Authors:  Yueh Chien; Shih-Jie Chou; Yuh-Lih Chang; Hsin-Bang Leu; Yi-Ping Yang; Ping-Hsing Tsai; Ying-Hsiu Lai; Kuan-Hsuan Chen; Wei-Chao Chang; Shih-Hsien Sung; Wen-Chung Yu
Journal:  Int J Mol Sci       Date:  2018-05-16       Impact factor: 5.923

10.  A Human Stem Cell Model of Fabry Disease Implicates LIMP-2 Accumulation in Cardiomyocyte Pathology.

Authors:  Matthew J Birket; Sophie Raibaud; Miriam Lettieri; Antony D Adamson; Valerie Letang; Pauline Cervello; Nicolas Redon; Gwenaelle Ret; Sandra Viale; Bing Wang; Bruno Biton; Jean-Claude Guillemot; Vincent Mikol; John P Leonard; Neil A Hanley; Cecile Orsini; Jean-Michel Itier
Journal:  Stem Cell Reports       Date:  2019-08-01       Impact factor: 7.765

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