Established and emerging roles for mitochondria in neutrophils.

Peng, Shuang; Gao, Jian; Stojkov, Darko; Yousefi, Shida; Simon, Hans-Uwe (2023). Established and emerging roles for mitochondria in neutrophils. Immunological reviews, 314(1), pp. 413-426. Wiley-Blackwell 10.1111/imr.13158

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Neutrophils are the most abundant innate immune cells in human blood, emerging as important players in a variety of diseases. Mitochondria are bioenergetic, biosynthetic, and signaling organelles critical for cell fate and function. Mitochondria have been overlooked in neutrophil research owing to the conventional view that neutrophils contain few, if any, competent mitochondria and do not rely on these organelles for adenosine triphosphate production. A growing body of evidence suggests that mitochondria participate in neutrophil biology at many levels, ranging from neutrophil development to chemotaxis, effector function, and cell death. Moreover, mitochondria and mitochondrial components, such as mitochondrial deoxyribonucleic acid, can be released by neutrophils to eliminate infection and/or shape immune response, depending on the specific context. In this review, we provide an update on the functional role of mitochondria in neutrophils, highlight mitochondria as key players in modulating the neutrophil phenotype and function during infection and inflammation, and discuss the possibilities and challenges to exploit the unique aspects of mitochondria in neutrophils for disease treatment.

Item Type:

Journal Article (Review Article)

Division/Institute:

04 Faculty of Medicine > Pre-clinic Human Medicine > Institute of Pharmacology

UniBE Contributor:

Peng, Shuang, Stojkov, Darko, Yousefi, Shida, Simon, Hans-Uwe

Subjects:

600 Technology > 610 Medicine & health

ISSN:

0105-2896

Publisher:

Wiley-Blackwell

Language:

English

Submitter:

Pubmed Import

Date Deposited:

08 Nov 2022 12:56

Last Modified:

29 Mar 2023 00:12

Publisher DOI:

10.1111/imr.13158

PubMed ID:

36331270

Uncontrolled Keywords:

immune response infection inflammation mitochondria neutrophils

BORIS DOI:

10.48350/174519

URI:

https://boris.unibe.ch/id/eprint/174519

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