The endocannabinoid anandamide activates pro-resolving pathways in human primary macrophages by engaging both CB


Journal

FASEB journal : official publication of the Federation of American Societies for Experimental Biology
ISSN: 1530-6860
Titre abrégé: FASEB J
Pays: United States
ID NLM: 8804484

Informations de publication

Date de publication:
31 May 2024
Historique:
revised: 30 04 2024
received: 04 07 2023
accepted: 07 05 2024
medline: 27 5 2024
pubmed: 27 5 2024
entrez: 27 5 2024
Statut: ppublish

Résumé

Resolution of inflammation is the cellular and molecular process that protects from widespread and uncontrolled inflammation and restores tissue function in the aftermath of acute immune events. This process is orchestrated by specialized pro-resolving mediators (SPM), a class of bioactive lipids able to reduce immune activation and promote removal of tissue debris and apoptotic cells by macrophages. Although SPMs are the lipid class that has been best studied for its role in facilitating the resolution of self-limited inflammation, a number of other lipid signals, including endocannabinoids, also exert protective immunomodulatory effects on immune cells, including macrophages. These observations suggest that endocannabinoids may also display pro-resolving actions. Interestingly, the endocannabinoid anandamide (AEA) is not only known to bind canonical type 1 and type 2 cannabinoid receptors (CB

Identifiants

pubmed: 38801406
doi: 10.1096/fj.202301325R
doi:

Substances chimiques

Endocannabinoids 0
anandamide UR5G69TJKH
Receptor, Cannabinoid, CB2 0
Polyunsaturated Alkamides 0
Arachidonic Acids 0
Receptors, G-Protein-Coupled 0
GPR18 protein, human 0
Docosahexaenoic Acids 25167-62-8
Arachidonate 5-Lipoxygenase EC 1.13.11.34
CNR2 protein, human 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e23675

Subventions

Organisme : Ministero della Salute
ID : PNRR-MAD-2022-12376730

Informations de copyright

© 2024 The Author(s). The FASEB Journal published by Wiley Periodicals LLC on behalf of Federation of American Societies for Experimental Biology.

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Auteurs

Alessandro Leuti (A)

Department of Medicine, Campus Bio-Medico University of Rome, Rome, Italy.
European Center for Brain Research/Institute for Research and Health Care (IRCCS) Santa Lucia Foundation, Rome, Italy.

Marina Fava (M)

European Center for Brain Research/Institute for Research and Health Care (IRCCS) Santa Lucia Foundation, Rome, Italy.

Giulia Forte (G)

Department of Medicine, Campus Bio-Medico University of Rome, Rome, Italy.

Niccolò Pellegrini (N)

Department of Medicine, Campus Bio-Medico University of Rome, Rome, Italy.

Sergio Oddi (S)

European Center for Brain Research/Institute for Research and Health Care (IRCCS) Santa Lucia Foundation, Rome, Italy.
Department of Veterinary Medicine, University of Teramo, Teramo, Italy.

Lucia Scipioni (L)

European Center for Brain Research/Institute for Research and Health Care (IRCCS) Santa Lucia Foundation, Rome, Italy.
Department of Biotechnological and Applied Clinical Sciences, University of L'Aquila, L'Aquila, Italy.

Esteban A Gomez (EA)

Centre for Inflammation and Therapeutic Innovation, Queen Mary University of London, London, UK.

Jesmond Dalli (J)

Centre for Inflammation and Therapeutic Innovation, Queen Mary University of London, London, UK.
William Harvey Research Institute, Queen Mary University of London, London, UK.

Mauro Maccarrone (M)

European Center for Brain Research/Institute for Research and Health Care (IRCCS) Santa Lucia Foundation, Rome, Italy.
Department of Biotechnological and Applied Clinical Sciences, University of L'Aquila, L'Aquila, Italy.

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