The role of efferocytosis-fueled macrophage metabolism in the resolution of inflammation.


Journal

Immunological reviews
ISSN: 1600-065X
Titre abrégé: Immunol Rev
Pays: England
ID NLM: 7702118

Informations de publication

Date de publication:
10 2023
Historique:
received: 02 03 2023
accepted: 20 04 2023
pmc-release: 01 10 2024
medline: 30 10 2023
pubmed: 9 5 2023
entrez: 9 5 2023
Statut: ppublish

Résumé

The phagocytosis of dying cells by macrophages, termed efferocytosis, is a tightly regulated process that involves the sensing, binding, engulfment, and digestion of apoptotic cells. Efferocytosis not only prevents tissue necrosis and inflammation caused by secondary necrosis of dying cells, but it also promotes pro-resolving signaling in macrophages, which is essential for tissue resolution and repair following injury or inflammation. An important factor that contributes to this pro-resolving reprogramming is the cargo that is released from apoptotic cells after their engulfment and phagolysosomal digestion by macrophages. The apoptotic cell cargo contains amino acids, nucleotides, fatty acids, and cholesterol that function as metabolites and signaling molecules to bring about this re-programming. Here, we review efferocytosis-induced changes in macrophage metabolism that mediate the pro-resolving functions of macrophages. We also discuss various strategies, challenges, and future perspectives related to drugging efferocytosis-fueled macrophage metabolism as strategy to dampen inflammation and promote resolution in chronic inflammatory diseases.

Identifiants

pubmed: 37158427
doi: 10.1111/imr.13214
pmc: PMC10615666
mid: NIHMS1896610
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

65-80

Subventions

Organisme : American Heart Association-American Stroke Association
ID : 900337
Pays : United States
Organisme : NHLBI NIH HHS
ID : P01 HL087123
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL159012
Pays : United States
Organisme : NHLBI NIH HHS
ID : R35 HL145228
Pays : United States

Informations de copyright

© 2023 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

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Auteurs

Maaike Schilperoort (M)

Department of Medicine, Columbia University Irving Medical Center, New York, New York, USA.

David Ngai (D)

Department of Medicine, Columbia University Irving Medical Center, New York, New York, USA.

Santosh R Sukka (SR)

Department of Medicine, Columbia University Irving Medical Center, New York, New York, USA.

Kleopatra Avrampou (K)

Department of Medicine, Columbia University Irving Medical Center, New York, New York, USA.

Hongxue Shi (H)

Department of Medicine, Columbia University Irving Medical Center, New York, New York, USA.

Ira Tabas (I)

Department of Medicine, Columbia University Irving Medical Center, New York, New York, USA.
Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, New York, USA.
Department of Physiology, Columbia University Irving Medical Center, New York, New York, USA.

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