Effects of lipoic acid on primary murine microglial cells.


Journal

Journal of neuroimmunology
ISSN: 1872-8421
Titre abrégé: J Neuroimmunol
Pays: Netherlands
ID NLM: 8109498

Informations de publication

Date de publication:
15 09 2019
Historique:
received: 08 03 2019
revised: 09 05 2019
accepted: 24 05 2019
pubmed: 9 6 2019
medline: 12 6 2020
entrez: 9 6 2019
Statut: ppublish

Résumé

The anti-oxidant lipoic acid (LA) is beneficial in murine models of multiple sclerosis (MS) and has recently been shown to slow brain atrophy in secondary progressive MS. The mechanism of these effects by LA is incompletely understood but may involve effects on microglia. The objective of this study is to understand how LA affects microglial cells. We cultured primary microglial cells from C57BL/6 adult mice brains and stimulated the cells with lipopolysaccharide (LPS) and interferon gamma (IFN-γ) in the presence or absence of LA. We demonstrate the inhibition of phagocytosis, rearrangement of actin, and formation of membrane blebs in stimulated microglia in the presence of LA. These experiments suggest that LA causes changes in microglial actin, which may lead to alterations in phagocytosis, mobility, and migration.

Identifiants

pubmed: 31176014
pii: S0165-5728(19)30106-7
doi: 10.1016/j.jneuroim.2019.576972
pmc: PMC6660368
mid: NIHMS1531190
pii:
doi:

Substances chimiques

Antioxidants 0
Lipopolysaccharides 0
Thioctic Acid 73Y7P0K73Y
Interferon-gamma 82115-62-6

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

576972

Subventions

Organisme : NINDS NIH HHS
ID : P30 NS061800
Pays : United States
Organisme : NINDS NIH HHS
ID : R01 NS057433
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR002369
Pays : United States

Informations de copyright

Copyright © 2019 Elsevier B.V. All rights reserved.

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Auteurs

Priya Chaudhary (P)

Department of Neurology, L226, Oregon Health & Science University, 3181 SW Sam Jackson Park Road, Portland, OR 97239, United States of America. Electronic address: chaudhar@ohsu.edu.

Gail Marracci (G)

Department of Neurology, L226, Oregon Health & Science University, 3181 SW Sam Jackson Park Road, Portland, OR 97239, United States of America; Research, VA Portland Health Care System, 3710 SW U.S. Veterans Hospital Road, Portland, OR 97239, United States of America.

Edvinas Pocius (E)

Department of Neurology, L226, Oregon Health & Science University, 3181 SW Sam Jackson Park Road, Portland, OR 97239, United States of America.

Danielle Galipeau (D)

Department of Neurology, L226, Oregon Health & Science University, 3181 SW Sam Jackson Park Road, Portland, OR 97239, United States of America.

Brooke Morris (B)

Department of Neurology, L226, Oregon Health & Science University, 3181 SW Sam Jackson Park Road, Portland, OR 97239, United States of America.

Dennis Bourdette (D)

Department of Neurology, L226, Oregon Health & Science University, 3181 SW Sam Jackson Park Road, Portland, OR 97239, United States of America; Research, VA Portland Health Care System, 3710 SW U.S. Veterans Hospital Road, Portland, OR 97239, United States of America.

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Classifications MeSH