Microglia are less pro‐inflammatory than myeloid infiltrates in the hippocampus of mice exposed to status epilepticus
Male
Epileptogenesis; Metalloproteinases; Pilocarpine; Pro-inflammatory cytokines; Temporal lobe epilepsy; Cellular and Molecular Neuroscience; Neurology
Interleukin-1beta
Piriform Cortex
pro-inflammatory cytokines
Hippocampus
metalloproteinases
RAT HIPPOCAMPUS
Mice
03 medical and health sciences
Status Epilepticus
0302 clinical medicine
Matrix Metalloproteinase 12
Proto-Oncogene Proteins
TEMPORAL-LOBE EPILEPSY
Animals
Myeloid Cells
CD40 Antigens
TUMOR-NECROSIS-FACTOR
BLOOD-BRAIN-BARRIER
CENTRAL-NERVOUS-SYSTEM
Pilocarpine
FACTOR-ALPHA
Receptor Protein-Tyrosine Kinases
temporal lobe epilepsy
GLUTAMATE UPTAKE
TNF-ALPHA
Axl Receptor Tyrosine Kinase
pilocarpine
Disease Models, Animal
Matrix Metalloproteinase 9
Astrocytes
ACID
epileptogenesis
SEIZURES
Microglia
DOI:
10.1002/glia.23008
Publication Date:
2016-06-01T05:36:49Z
AUTHORS (10)
ABSTRACT
Activated microglia, astrogliosis, expression of pro-inflammatory cytokines, blood brain barrier (BBB) leakage and peripheral immune cell infiltration are features mesial temporal lobe epilepsy. Numerous studies correlated the cytokines with activated morphology attributing them a pro-epileptogenic role. However, microglia myeloid cells such as macrophages have always been difficult to distinguish due an overlap in expressed surface molecules. Thus, detrimental role epilepsy that is attributed might be shared infiltrates. Here, we used FACS-based approach discriminate between infiltrates isolated from hippocampus 24 h 96 after status epilepticus (SE) pilocarpine-treated CD1 mice. We observed do not express MHCII whereas high levels CD40 SE. This antigen-presenting phenotype presence CD4(pos) T cells. Moreover, only TNFα SE while IL-1β TNFα. Immunofluorescence showed astrocytes but IL-1β. Myeloid also matrix metalloproteinase (MMP)-9 12 MMP-12, suggesting involvement both types BBB follows Finally, phagocytosis receptor Axl, pointing apoptotic one main functions microglia. Our data suggests that, during early epileptogenesis, remain rather supressed display strong inflammatory profile. GLIA 2016 2016;64:1350-1362.
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