Clock-Controlled Mitochondrial Dynamics Correlates with Cyclic Pregnenolone Synthesis.


Journal

Cells
ISSN: 2073-4409
Titre abrégé: Cells
Pays: Switzerland
ID NLM: 101600052

Informations de publication

Date de publication:
19 10 2020
Historique:
received: 01 10 2020
revised: 15 10 2020
accepted: 16 10 2020
entrez: 22 10 2020
pubmed: 23 10 2020
medline: 7 4 2021
Statut: epublish

Résumé

Neurosteroids are steroids synthetized in the nervous system, with the first step of steroidogenesis taking place within mitochondria with the synthesis of pregnenolone. They exert important brain-specific functions by playing a role in neurotransmission, learning and memory processes, and neuroprotection. Here, we show for the first time that mitochondrial neurosteroidogenesis follows a circadian rhythm and correlates with the rhythmic changes in mitochondrial morphology. We used synchronized human A172 glioma cells, which are steroidogenic cells with a functional core molecular clock, to show that pregnenolone levels and translocator protein (TSPO) are controlled by the clock, probably via circadian regulation of mitochondrial fusion/fission. Key findings were recapitulated in mouse brains. We also showed that genetic or pharmacological abrogation of fusion/fission activity, as well as disturbing the core molecular clock, abolished circadian rhythms of pregnenolone and TSPO. Our findings provide new insights into the crosstalk between mitochondrial function (here, neurosteroidogenesis) and circadian cycles.

Identifiants

pubmed: 33086741
pii: cells9102323
doi: 10.3390/cells9102323
pmc: PMC7589815
pii:
doi:

Substances chimiques

Receptors, GABA 0
TSPO protein, human 0
Pregnenolone 73R90F7MQ8

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Melissa Witzig (M)

Neurobiology Lab for Brain Aging and Mental Health, Molecular & Cognitive Neuroscience, Transfaculty Research Platform, University of Basel, 4002 Basel, Switzerland.
Psychiatric University Clinics Basel, Medical Faculty, University of Basel, 4002 Basel, Switzerland.

Amandine Grimm (A)

Neurobiology Lab for Brain Aging and Mental Health, Molecular & Cognitive Neuroscience, Transfaculty Research Platform, University of Basel, 4002 Basel, Switzerland.
Psychiatric University Clinics Basel, Medical Faculty, University of Basel, 4002 Basel, Switzerland.
Division of Molecular Psychology, Live Sciences Training Facility, University of Basel, 4055 Basel, Switzerland.

Karen Schmitt (K)

Neurobiology Lab for Brain Aging and Mental Health, Molecular & Cognitive Neuroscience, Transfaculty Research Platform, University of Basel, 4002 Basel, Switzerland.
Psychiatric University Clinics Basel, Medical Faculty, University of Basel, 4002 Basel, Switzerland.

Imane Lejri (I)

Neurobiology Lab for Brain Aging and Mental Health, Molecular & Cognitive Neuroscience, Transfaculty Research Platform, University of Basel, 4002 Basel, Switzerland.
Psychiatric University Clinics Basel, Medical Faculty, University of Basel, 4002 Basel, Switzerland.

Stephan Frank (S)

Division of Neuropathology, Institute of Pathology, University Hospital Basel, 4031 Basel, Switzerland.

Steven A Brown (SA)

Chronobiology and Sleep Research Group, Institute of Pharmacology and Toxicology, University of Zürich, 8057 Zürich, Switzerland.

Anne Eckert (A)

Neurobiology Lab for Brain Aging and Mental Health, Molecular & Cognitive Neuroscience, Transfaculty Research Platform, University of Basel, 4002 Basel, Switzerland.
Psychiatric University Clinics Basel, Medical Faculty, University of Basel, 4002 Basel, Switzerland.

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Classifications MeSH