Glia Maturation Factor (GMF) Regulates Microglial Expression Phenotypes and the Associated Neurological Deficits in a Mouse Model of Traumatic Brain Injury.
Animals
Biomarkers
/ metabolism
Brain
/ pathology
Brain Injuries, Traumatic
/ pathology
Calcium-Binding Proteins
/ metabolism
Cognition
Cytokines
/ metabolism
Cytoskeletal Proteins
/ metabolism
Disease Models, Animal
Glia Maturation Factor
/ deficiency
Gliosis
/ complications
Macrophages
/ metabolism
Membrane Proteins
/ metabolism
Mice, Inbred C57BL
Mice, Knockout
Microfilament Proteins
/ metabolism
Microglia
/ metabolism
Motor Activity
Neurons
/ metabolism
Oxidative Stress
Phenotype
Phosphorylation
Glia maturation factor
M1-like
M2-like
Microglia/macrophage
Neuroinflammation
Polarization
Traumatic brain injury
Journal
Molecular neurobiology
ISSN: 1559-1182
Titre abrégé: Mol Neurobiol
Pays: United States
ID NLM: 8900963
Informations de publication
Date de publication:
Nov 2020
Nov 2020
Historique:
received:
26
03
2020
accepted:
24
07
2020
pubmed:
2
8
2020
medline:
30
6
2021
entrez:
2
8
2020
Statut:
ppublish
Résumé
Traumatic brain injury (TBI) induces inflammatory responses through microglial activation and polarization towards a more inflammatory state that contributes to the deleterious secondary brain injury. Glia maturation factor (GMF) is a pro-inflammatory protein that is responsible for neuroinflammation following insult to the brain, such as in TBI. We hypothesized that the absence of GMF in GMF-knockout (GMF-KO) mice would regulate microglial activation state and the M1/M2 phenotypes following TBI. We used the weight drop model of TBI in C57BL/6 mice wild-type (WT) and GMF-KO mice. Immunofluorescence staining, Western blot, and ELISA assays were performed to confirm TBI-induced histopathological and neuroinflammatory changes. Behavioral analysis was done to check motor coordination ability and cognitive function. We demonstrated that the deletion of GMF in GMF-KO mice significantly limited lesion volume, attenuated neuronal loss, inhibited gliosis, and activated microglia adopted predominantly anti-inflammatory (M2) phenotypes. Using an ELISA method, we found a gradual decrease in pro-inflammatory cytokines (TNF-α and IL-6) and upregulation of anti-inflammatory cytokines (IL-4 and IL-10) in GMF-KO mice compared with WT mice, thus, promoting the transition of microglia towards a more predominantly anti-inflammatory (M2) phenotype. GMF-KO mice showed significant improvement in motor ability, memory, and cognition. Overall, our results demonstrate that GMF deficiency regulates microglial polarization, which ameliorates neuronal injury and behavioral impairments following TBI in mice and concludes that GMF is a regulator of neuroinflammation and an ideal therapeutic target for the treatment of TBI.
Identifiants
pubmed: 32737763
doi: 10.1007/s12035-020-02040-y
pii: 10.1007/s12035-020-02040-y
doi:
Substances chimiques
Aif1 protein, mouse
0
Biomarkers
0
Calcium-Binding Proteins
0
Cytokines
0
Cytoskeletal Proteins
0
Glia Maturation Factor
0
Membrane Proteins
0
Microfilament Proteins
0
ezrin
0
moesin
144131-77-1
radixin
144517-21-5
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
4438-4450Subventions
Organisme : BLRD VA
ID : I01 BX002477
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG048205
Pays : United States
Organisme : NINDS NIH HHS
ID : R01 NS073670
Pays : United States
Organisme : NINDS NIH HHS
ID : R01 NS086929
Pays : United States