Induced pluripotent stem cells derived from patients carrying mitochondrial mutations exhibit altered bioenergetics and aberrant differentiation potential

被引:0
作者
Fibi Meshrkey
Kelly M. Scheulin
Christopher M. Littlejohn
Joshua Stabach
Bibhuti Saikia
Vedant Thorat
Yimin Huang
Thomas LaFramboise
Edward J. Lesnefsky
Raj R. Rao
Franklin D. West
Shilpa Iyer
机构
[1] University of Arkansas,Department of Biological Sciences, J. William Fulbright College of Arts and Sciences
[2] University of Arkansas,Cell and Molecular Biology Program
[3] Alexandria University,Department of Histology and Cell Biology, Faculty of Medicine
[4] University of Georgia,Regenerative Bioscience Center
[5] University of Georgia,Department of Animal and Dairy Science
[6] University of Georgia,Neuroscience Program, Biomedical and Health Sciences Institute
[7] Case Western Reserve University School of Medicine,Department of Genetics and Genome Sciences
[8] Virginia Commonwealth University,Department of Physiology and Biophysics
[9] McGuire Veterans Affairs Medical Center,Cardiology Section Medical Service
[10] Virginia Commonwealth University,Department of Biochemistry and Molecular Biology
[11] Virginia Commonwealth University,Division of Cardiology, Department of Internal Medicine, Pauley Heart Center
[12] University of Arkansas,Department of Biomedical Engineering, College of Engineering
来源
Stem Cell Research & Therapy | / 14卷
关键词
Mitochondrial disease; hiPSC; Pluripotent stem cell; Reprogramming; Bioenergetics; Respiration; Differentiation;
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  • [1] Iyer S(2009)Stem cell-based models and therapies for neurodegenerative diseases Crit Rev Biomed Eng 37 321-353
  • [2] Alsayegh K(2002)Frequent intracellular clonal expansions of somatic mtDNA mutations: significance and mechanisms Ann N Y Acad Sci 959 434-447
  • [3] Abraham S(2002)Clonally expanded mtDNA point mutations are abundant in individual cells of human tissues Proc Natl Acad Sci 99 5521-5526
  • [4] Rao RR(2002)mtLOH (mitochondrial loss of heteroplasmy), aging, and 'surrogate self' Mech Ageing Dev 123 891-898
  • [5] Coller HA(1998)Recent developments in the molecular genetics of mitochondrial disorders J Neurol Sci 153 251-263
  • [6] Bodyak ND(2014)Mitochondria, energetics, epigenetics, and cellular responses to stress Environ Health Perspect 122 1271-1278
  • [7] Khrapko K(2016)Mitochondrial Genome and Longevity Biochemistry (Mosc) 81 1401-1405
  • [8] Nekhaeva E(2013)OXPHOS mutations and neurodegeneration EMBO J 32 9-29
  • [9] Bodyak ND(1995)Molecular genetic aspects of human mitochondrial disorders Annu Rev Genet 29 151-178
  • [10] Kraytsberg Y(2004)De novo mutations in the mitochondrial ND3 gene as a cause of infantile mitochondrial encephalopathy and complex I deficiency Ann Neurol 55 58-64