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Pluripotent Stem Cells for Uncovering the Role of Mitochondria in Human Brain Function and Dysfunction
Authors:Annika Zink  Josef Priller  Alessandro Prigione
Affiliation:1. Max Delbrueck Center for Molecular Medicine (MDC), 13125 Berlin, Germany;2. Department of Neuropsychiatry, Charité—Universitätsmedizin, 10117 Berlin, Germany;3. Berlin Institute of Health (BIH), 10178 Berlin, Germany;4. Cluster of Excellence NeuroCure and German Center for Neurodegenerative Diseases (DZNE), 10117 Berlin, Germany;5. UK Dementia Research Institute and University of Edinburgh, Edinburgh EH16 4SB, UK
Abstract:Mitochondrial dysfunctions are a known pathogenetic mechanism of a number of neurological and psychiatric disorders. At the same time, mutations in genes encoding for components of the mitochondrial respiratory chain cause mitochondrial diseases, which commonly exhibit neurological symptoms. Mitochondria are therefore critical for the functionality of the human nervous system. The importance of mitochondria stems from their key roles in cellular metabolism, calcium handling, redox and protein homeostasis, and overall cellular homeostasis through their dynamic network. Here, we describe how the use of pluripotent stem cells (PSCs) may help in addressing the physiological and pathological relevance of mitochondria for the human nervous system. PSCs allow the generation of patient-derived neurons and glia and the identification of gene-specific and mutation-specific cellular phenotypes via genome engineering approaches. We discuss the recent advances in PSC-based modeling of brain diseases and the current challenges of the field. We anticipate that the careful use of PSCs will improve our understanding of the impact of mitochondria in neurological and psychiatric disorders and the search for effective therapeutic avenues.
Keywords:mitochondria  iPSCs  genome editing  neurological disorders  mitochondrial diseases  PSCs  pluripotent stem cells  OxPhos  oxidative phosphorylation  RC  respiratory chain  MMP  mitochondrial membrane potential  ROS  reactive oxygen species  CNS  central nervous system  PPP  pentose phosphate pathway  GSH  glutathione  AD  Alzheimer's disease  PD  Parkinson's disease  ALS  amyotrophic lateral sclerosis  HD  Huntington's disease  HTT  huntingtin  SCZ  schizophrenia  BPD  bipolar disorder  ASD  autism spectrum disorder  nDNA  nuclear DNA  mtDNA  mitochondrial DNA  MELAS  mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes  LS  Leigh syndrome  iPSCs  induced pluripotent stem cells  CRISPR  clustered regularly interspaced short palindromic repeats
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