Microglia moonlighting after traumatic brain injury: aging and interferons influence chronic microglia reactivity.


Journal

Trends in neurosciences
ISSN: 1878-108X
Titre abrégé: Trends Neurosci
Pays: England
ID NLM: 7808616

Informations de publication

Date de publication:
11 2023
Historique:
received: 12 06 2023
revised: 11 08 2023
accepted: 24 08 2023
pmc-release: 01 11 2024
medline: 23 10 2023
pubmed: 19 9 2023
entrez: 18 9 2023
Statut: ppublish

Résumé

Most of the individuals who experience traumatic brain injury (TBI) develop neuropsychiatric and cognitive complications that negatively affect recovery and health span. Activation of multiple inflammatory pathways persists after TBI, but it is unclear how inflammation contributes to long-term behavioral and cognitive deficits. One outcome of TBI is microglial priming and subsequent hyper-reactivity to secondary stressors, injuries, or immune challenges that further augment complications. Additionally, microglia priming with aging contributes to exaggerated glial responses to TBI. One prominent inflammatory pathway, interferon (IFN) signaling, is increased after TBI and may contribute to microglial priming and subsequent reactivity. This review discusses the contributions of microglia to inflammatory processes after TBI, as well as the influence of aging and IFNs on microglia reactivity and chronic inflammation after TBI.

Identifiants

pubmed: 37723009
pii: S0166-2236(23)00206-0
doi: 10.1016/j.tins.2023.08.008
pmc: PMC10592045
mid: NIHMS1927683
pii:
doi:

Substances chimiques

Interferons 9008-11-1

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

926-940

Subventions

Organisme : NINDS NIH HHS
ID : R01 NS118037
Pays : United States

Informations de copyright

Copyright © 2023 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests The authors declare no competing interests in relation to this work.

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Auteurs

Lynde M Wangler (LM)

Department of Neuroscience, The Ohio State University Wexner Medical Center, 333 W 10th Ave, Columbus, OH, USA.

Jonathan P Godbout (JP)

Department of Neuroscience, The Ohio State University Wexner Medical Center, 333 W 10th Ave, Columbus, OH, USA; Institute for Behavioral Medicine Research, Ohio State University Wexner Medical Center, 460 Medical Center Drive, Columbus, OH, USA; Chronic Brain Injury Program, The Ohio State University, 190 North Oval Mall, Columbus, OH, USA. Electronic address: Jonathan.Godbout@osumc.edu.

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