Mitochondrial Fission Governed by Drp1 Regulates Exogenous Fatty Acid Usage and Storage in Hela Cells.

fatty acid oxidation lipid homeostasis mitochondrial dynamics

Journal

Metabolites
ISSN: 2218-1989
Titre abrégé: Metabolites
Pays: Switzerland
ID NLM: 101578790

Informations de publication

Date de publication:
18 May 2021
Historique:
received: 20 04 2021
revised: 10 05 2021
accepted: 13 05 2021
entrez: 2 6 2021
pubmed: 3 6 2021
medline: 3 6 2021
Statut: epublish

Résumé

In the presence of high abundance of exogenous fatty acids, cells either store fatty acids in lipid droplets or oxidize them in mitochondria. In this study, we aimed to explore a novel and direct role of mitochondrial fission in lipid homeostasis in HeLa cells. We observed the association between mitochondrial morphology and lipid droplet accumulation in response to high exogenous fatty acids. We inhibited mitochondrial fission by silencing dynamin-related protein 1(DRP1) and observed the shift in fatty acid storage-usage balance. Inhibition of mitochondrial fission resulted in an increase in fatty acid content of lipid droplets and a decrease in mitochondrial fatty acid oxidation. Next, we overexpressed carnitine palmitoyltransferase-1 (CPT1), a key mitochondrial protein in fatty acid oxidation, to further examine the relationship between mitochondrial fatty acid usage and mitochondrial morphology. Mitochondrial fission plays a role in distributing exogenous fatty acids. CPT1A controlled the respiratory rate of mitochondrial fatty acid oxidation but did not cause a shift in the distribution of fatty acids between mitochondria and lipid droplets. Our data reveals a novel function for mitochondrial fission in balancing exogenous fatty acids between usage and storage, assigning a role for mitochondrial dynamics in control of intracellular fuel utilization and partitioning.

Identifiants

pubmed: 34069800
pii: metabo11050322
doi: 10.3390/metabo11050322
pmc: PMC8157282
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Hungarian National Research, Development and Innovation Office
ID : NKFI-KPP-126998
Organisme : NIDDK NIH HHS
ID : R01 DK110181
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK127637
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30 DK045735
Pays : United States
Organisme : NIH HHS
ID : AG052005, AG052986, AG051459, DK111178, DK045735, DK097566, DK110181, DK045735-26
Pays : United States

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Auteurs

Jae-Eun Song (JE)

Yale Program in Integrative Cell Signaling and Neurobiology of Metabolism, Department of Comparative Medicine, Yale University School of Medicine, New Haven, CT 06511, USA.

Tiago C Alves (TC)

Laboratory Medicine, Institute for Clinical Chemistry, Technische Universität Dresden, 01069 Dresden, Germany.

Bernardo Stutz (B)

Yale Program in Integrative Cell Signaling and Neurobiology of Metabolism, Department of Comparative Medicine, Yale University School of Medicine, New Haven, CT 06511, USA.

Matija Šestan-Peša (M)

Yale Program in Integrative Cell Signaling and Neurobiology of Metabolism, Department of Comparative Medicine, Yale University School of Medicine, New Haven, CT 06511, USA.

Nicole Kilian (N)

Centre for Infectious Diseases, Parasitology, Heidelberg University Hospital, 69120 Heidelberg, Germany.

Sungho Jin (S)

Institute of Human Nutrition, Columbia University Irving Medical Center, New York, NY 10032, USA.
Department of Molecular Pharmacology and Therapeutics, Columbia University Irving Medical Center, New York, NY 10032, USA.

Sabrina Diano (S)

Institute of Human Nutrition, Columbia University Irving Medical Center, New York, NY 10032, USA.
Department of Molecular Pharmacology and Therapeutics, Columbia University Irving Medical Center, New York, NY 10032, USA.

Richard G Kibbey (RG)

Department of Internal Medicine, Yale University School of Medicine, New Haven, CT 06511, USA.

Tamas L Horvath (TL)

Yale Program in Integrative Cell Signaling and Neurobiology of Metabolism, Department of Comparative Medicine, Yale University School of Medicine, New Haven, CT 06511, USA.
Department of Neuroscience, Yale University School of Medicine, New Haven, CT 06511, USA.
Department of Ob/Gyn & Reproductive Sciences, Yale University School of Medicine, New Haven, CT 06511, USA.

Classifications MeSH