Microglia are an essential component of the neuroprotective scar that forms after spinal cord injury.


Journal

Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555

Informations de publication

Date de publication:
31 01 2019
Historique:
received: 13 08 2018
accepted: 08 01 2019
entrez: 2 2 2019
pubmed: 2 2 2019
medline: 9 4 2019
Statut: epublish

Résumé

The role of microglia in spinal cord injury (SCI) remains poorly understood and is often confused with the response of macrophages. Here, we use specific transgenic mouse lines and depleting agents to understand the response of microglia after SCI. We find that microglia are highly dynamic and proliferate extensively during the first two weeks, accumulating around the lesion. There, activated microglia position themselves at the interface between infiltrating leukocytes and astrocytes, which proliferate and form a scar in response to microglia-derived factors, such as IGF-1. Depletion of microglia after SCI causes disruption of glial scar formation, enhances parenchymal immune infiltrates, reduces neuronal and oligodendrocyte survival, and impairs locomotor recovery. Conversely, increased microglial proliferation, induced by local M-CSF delivery, reduces lesion size and enhances functional recovery. Altogether, our results identify microglia as a key cellular component of the scar that develops after SCI to protect neural tissue.

Identifiants

pubmed: 30705270
doi: 10.1038/s41467-019-08446-0
pii: 10.1038/s41467-019-08446-0
pmc: PMC6355913
doi:

Substances chimiques

Insulin-Like Growth Factor I 67763-96-6

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

518

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Auteurs

Victor Bellver-Landete (V)

Axe neurosciences du Centre de recherche du Centre hospitalier universitaire (CHU) de Québec-Université Laval et Département de médecine moléculaire de l'Université Laval, Québec, QC, G1V 4G2, Canada.

Floriane Bretheau (F)

Axe neurosciences du Centre de recherche du Centre hospitalier universitaire (CHU) de Québec-Université Laval et Département de médecine moléculaire de l'Université Laval, Québec, QC, G1V 4G2, Canada.

Benoit Mailhot (B)

Axe neurosciences du Centre de recherche du Centre hospitalier universitaire (CHU) de Québec-Université Laval et Département de médecine moléculaire de l'Université Laval, Québec, QC, G1V 4G2, Canada.

Nicolas Vallières (N)

Axe neurosciences du Centre de recherche du Centre hospitalier universitaire (CHU) de Québec-Université Laval et Département de médecine moléculaire de l'Université Laval, Québec, QC, G1V 4G2, Canada.

Martine Lessard (M)

Axe neurosciences du Centre de recherche du Centre hospitalier universitaire (CHU) de Québec-Université Laval et Département de médecine moléculaire de l'Université Laval, Québec, QC, G1V 4G2, Canada.

Marie-Eve Janelle (ME)

Département de biologie-biotechnologie du Cégep de Lévis-Lauzon, Lévis, QC, Canada, G6V 6Z9.

Nathalie Vernoux (N)

Axe neurosciences du Centre de recherche du Centre hospitalier universitaire (CHU) de Québec-Université Laval et Département de médecine moléculaire de l'Université Laval, Québec, QC, G1V 4G2, Canada.

Marie-Ève Tremblay (MÈ)

Axe neurosciences du Centre de recherche du Centre hospitalier universitaire (CHU) de Québec-Université Laval et Département de médecine moléculaire de l'Université Laval, Québec, QC, G1V 4G2, Canada.

Tobias Fuehrmann (T)

Department of Chemical Engineering & Applied Chemistry, University of Toronto, Toronto, ON, M5S 3E1, Canada.

Molly S Shoichet (MS)

Department of Chemical Engineering & Applied Chemistry, University of Toronto, Toronto, ON, M5S 3E1, Canada.

Steve Lacroix (S)

Axe neurosciences du Centre de recherche du Centre hospitalier universitaire (CHU) de Québec-Université Laval et Département de médecine moléculaire de l'Université Laval, Québec, QC, G1V 4G2, Canada. Steve.Lacroix@crchul.ulaval.ca.

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