Dorsal Root Ganglia Macrophages Maintain Osteoarthritis Pain.


Journal

The Journal of neuroscience : the official journal of the Society for Neuroscience
ISSN: 1529-2401
Titre abrégé: J Neurosci
Pays: United States
ID NLM: 8102140

Informations de publication

Date de publication:
29 09 2021
Historique:
received: 10 07 2020
revised: 29 07 2021
accepted: 02 08 2021
pubmed: 18 8 2021
medline: 24 11 2021
entrez: 17 8 2021
Statut: ppublish

Résumé

Pain is the major debilitating symptom of osteoarthritis (OA), which is difficult to treat. In OA patients joint tissue damage only poorly associates with pain, indicating other mechanisms contribute to OA pain. Immune cells regulate the sensory system, but little is known about the involvement of immune cells in OA pain. Here, we report that macrophages accumulate in the dorsal root ganglia (DRG) distant from the site of injury in two rodent models of OA. DRG macrophages acquired an M1-like phenotype, and depletion of DRG macrophages resolved OA pain in male and female mice. Sensory neurons innervating the damaged knee joint shape DRG macrophages into an M1-like phenotype. Persisting OA pain, accumulation of DRG macrophages, and programming of DRG macrophages into an M1-like phenotype were independent of Na

Identifiants

pubmed: 34400519
pii: JNEUROSCI.1787-20.2021
doi: 10.1523/JNEUROSCI.1787-20.2021
pmc: PMC8482866
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

8249-8261

Subventions

Organisme : Wellcome Trust
ID : 200183/Z/15/Z
Pays : United Kingdom
Organisme : Versus Arthritis
ID : 21950
Pays : United Kingdom

Commentaires et corrections

Type : ErratumIn

Informations de copyright

Copyright © 2021 the authors.

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Auteurs

Ramin Raoof (R)

Center for Translational Immunology, University Medical Center Utrecht, Utrecht University, 3584 CX Utrecht, The Netherlands.

Christian Martin Gil (C)

Center for Translational Immunology, University Medical Center Utrecht, Utrecht University, 3584 CX Utrecht, The Netherlands.

Floris P J G Lafeber (FPJG)

Department of Rheumatology and Clinical Immunology, Regenerative Medicine Center, University Medical Center Utrecht, Utrecht University, 3584 CX Utrecht, The Netherlands.

Huub de Visser (H)

Department of Rheumatology and Clinical Immunology, Regenerative Medicine Center, University Medical Center Utrecht, Utrecht University, 3584 CX Utrecht, The Netherlands.

Judith Prado (J)

Center for Translational Immunology, University Medical Center Utrecht, Utrecht University, 3584 CX Utrecht, The Netherlands.

Sabine Versteeg (S)

Center for Translational Immunology, University Medical Center Utrecht, Utrecht University, 3584 CX Utrecht, The Netherlands.

Mirte N Pascha (MN)

Center for Translational Immunology, University Medical Center Utrecht, Utrecht University, 3584 CX Utrecht, The Netherlands.

Anne L P Heinemans (ALP)

Center for Translational Immunology, University Medical Center Utrecht, Utrecht University, 3584 CX Utrecht, The Netherlands.

Youri Adolfs (Y)

Department of Translational Neuroscience, Utrecht Brain Center, University Medical Center Utrecht, Utrecht University, 3584 CX Utrecht, The Netherlands.

Jeroen Pasterkamp (J)

Department of Translational Neuroscience, Utrecht Brain Center, University Medical Center Utrecht, Utrecht University, 3584 CX Utrecht, The Netherlands.

John N Wood (JN)

Molecular Nociception Group, Department of Biology, University College London, London WC1E 6BT, England.

Simon C Mastbergen (SC)

Department of Rheumatology and Clinical Immunology, Regenerative Medicine Center, University Medical Center Utrecht, Utrecht University, 3584 CX Utrecht, The Netherlands.

Niels Eijkelkamp (N)

Center for Translational Immunology, University Medical Center Utrecht, Utrecht University, 3584 CX Utrecht, The Netherlands n.eijkelkamp@umcutrecht.nl.

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Classifications MeSH