Single organelle analysis to characterize mitochondrial function and crosstalk during viral infection.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
11 06 2019
Historique:
received: 15 11 2018
accepted: 23 05 2019
entrez: 13 6 2019
pubmed: 13 6 2019
medline: 21 10 2020
Statut: epublish

Résumé

Mitochondria are key for cellular metabolism and signalling processes during viral infection. We report a methodology to analyse mitochondrial properties at the single-organelle level during viral infection using a recombinant adenovirus coding for a mitochondrial tracer protein for tagging and detection by multispectral flow cytometry. Resolution at the level of tagged individual mitochondria revealed changes in mitochondrial size, membrane potential and displayed a fragile phenotype during viral infection of cells. Thus, single-organelle and multi-parameter resolution allows to explore altered energy metabolism and antiviral defence by tagged mitochondria selectively in virus-infected cells and will be instrumental to identify viral immune escape and to develop and monitor novel mitochondrial-targeted therapies.

Identifiants

pubmed: 31186476
doi: 10.1038/s41598-019-44922-9
pii: 10.1038/s41598-019-44922-9
pmc: PMC6560178
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

8492

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Auteurs

Annika Schneider (A)

Institute of Molecular Immunology and Experimental Oncology, Klinikum rechts der Isar, Technical University of Munich, Munich, 81567, Germany.

Sandra Kurz (S)

Institute of Molecular Immunology and Experimental Oncology, Klinikum rechts der Isar, Technical University of Munich, Munich, 81567, Germany.

Katrin Manske (K)

Institute of Molecular Immunology and Experimental Oncology, Klinikum rechts der Isar, Technical University of Munich, Munich, 81567, Germany.

Marianne Janas (M)

Institute of Molecular Immunology and Experimental Oncology, Klinikum rechts der Isar, Technical University of Munich, Munich, 81567, Germany.

Mathias Heikenwälder (M)

Division of Chronic Inflammation and Cancer, German Cancer Research Center (DKFZ), Heidelberg, 69120, Germany.

Thomas Misgeld (T)

Institute of Neuronal Cell Biology, Technical University of Munich, Munich, Germany; German Center for Neurodegenerative Diseases, Munich, 80802, Germany.

Michaela Aichler (M)

Research Unit Analytical Pathology, Helmholtz Zentrum München, Ingolstädter Landstraße 1, Oberschleißheim, 85764, Germany.

Sebastian Felix Weissmann (SF)

Sony Biotechnology, Sony Europe Ltd., Weybridge, Surrey, KT13 0XW, UK.

Hans Zischka (H)

Institute of Molecular Toxicology and Pharmacology, Helmholtz Center Munich, German Research Center for Environmental Health, Neuherberg, 85764, Germany.
Institute of Toxicology and Environmental Hygiene, Technical University of Munich, Munich, 80802, Germany.

Percy Knolle (P)

Institute of Molecular Immunology and Experimental Oncology, Klinikum rechts der Isar, Technical University of Munich, Munich, 81567, Germany.

Dirk Wohlleber (D)

Institute of Molecular Immunology and Experimental Oncology, Klinikum rechts der Isar, Technical University of Munich, Munich, 81567, Germany. dirk.wohlleber@tum.de.

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Classifications MeSH