Pleiotropic Mitochondria: The Influence of Mitochondria on Neuronal Development and Disease.


Journal

The Journal of neuroscience : the official journal of the Society for Neuroscience
ISSN: 1529-2401
Titre abrégé: J Neurosci
Pays: United States
ID NLM: 8102140

Informations de publication

Date de publication:
16 10 2019
Historique:
received: 02 07 2019
revised: 09 08 2019
accepted: 10 08 2019
entrez: 18 10 2019
pubmed: 18 10 2019
medline: 4 7 2020
Statut: ppublish

Résumé

Mitochondria play many important biological roles, including ATP production, lipid biogenesis, ROS regulation, and calcium clearance. In neurons, the mitochondrion is an essential organelle for metabolism and calcium homeostasis. Moreover, mitochondria are extremely dynamic and able to divide, fuse, and move along microtubule tracks to ensure their distribution to the neuronal periphery. Mitochondrial dysfunction and altered mitochondrial dynamics are observed in a wide range of conditions, from impaired neuronal development to various neurodegenerative diseases. Novel imaging techniques and genetic tools provide unprecedented access to the physiological roles of mitochondria by visualizing mitochondrial trafficking, morphological dynamics, ATP generation, and ultrastructure. Recent studies using these new techniques have unveiled the influence of mitochondria on axon branching, synaptic function, calcium regulation with the ER, glial cell function, neurogenesis, and neuronal repair. This review provides an overview of the crucial roles played by mitochondria in the CNS in physiological and pathophysiological conditions.

Identifiants

pubmed: 31619488
pii: 39/42/8200
doi: 10.1523/JNEUROSCI.1157-19.2019
pmc: PMC6794931
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

8200-8208

Subventions

Organisme : NIGMS NIH HHS
ID : P20 GM103636
Pays : United States

Informations de copyright

Copyright © 2019 the authors.

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Auteurs

Vidhya Rangaraju (V)

Max Planck Institute for Brain Research, Frankfurt 60438, Germany.

Tommy L Lewis (TL)

Aging & Metabolism Program, Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma 73104.

Yusuke Hirabayashi (Y)

Department of Chemistry and Biotechnology, Graduate School of Engineering, University of Tokyo, 113-8656 Tokyo, Japan.
Japan Science and Technology Agency, Precursory Research for Embryonic Science and Technology, 332-0012 Saitama, Kawaguchi, Japan.

Matteo Bergami (M)

Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases, University Hospital Cologne, Cologne D-50931, Germany.
Institute of Genetics, University of Cologne, Cologne D-50674, Germany.
Center for Molecular Medicine, Cologne D-50931, Germany.

Elisa Motori (E)

Max Planck Institute for Biology of Ageing, Cologne D-50931, Germany.

Romain Cartoni (R)

Department of Pharmacology and Cancer Biology, Duke University School of Medicine, Durham, North Carolina 27710.
Department of Ophthalmology, Duke University School of Medicine, Durham, North Carolina 27710.

Seok-Kyu Kwon (SK)

Korea Institute of Science and Technology, Center for Functional Connectomics, Brain Science Institute, Seoul, South Korea 02792, and skkwon@kist.re.kr julien.courchet@univ-lyon1.fr.

Julien Courchet (J)

Université Claude Bernard Lyon 1, Centre National de la Recherche Scientifique Unité Mixte de Recherche-5310, Institut National de la Santé et de la Recherche Médicale U-1217, Institut NeuroMyoGène, F-69622, Villeurbanne, France skkwon@kist.re.kr julien.courchet@univ-lyon1.fr.

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