Abstract | AIM: METHODS: We performed transient middle cerebral artery occlusion (tMCAO) on C57BL/6J male mice and induced cultured BV2 microglia and primary bone marrow-derived macrophages to be M1/2 phenotype by LPS+ interferon-γ and IL-4, respectively. Immunofluorescence and flow cytometry were used for detecting the specialized protein expression of M1/2, such as CD206 and CD16/32. qPCR was utilized to detect the signature gene change of M1/2. RESULTS: GB significantly reduced cerebral ischemic damage and ameliorated the neurological deficits of mice after tMCAO. More importantly, our experiments proved that GB promoted microglia/macrophage transferring from inflammatory M1 phenotype to a protective, anti-inflammatory M2 phenotype in vivo or vitro. CV3988 and silencing the platelet activator factor (PAF) receptor by siRNA demonstrated that PAF receptor was involved in the modulation of microglia/macrophage polarization. CONCLUSION: Our results reveal a novel pharmacological effect of GB in modulating microglia/macrophage polarization after tMCAO, thus deepening our understanding of neuroprotective mechanisms of GB in treatment of ischemic stroke. Furthermore, this new mechanism may allow GB to be used in many other microglia/macrophage polarization-related inflammatory diseases.
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Authors | Zhao-Ma Shu, Xiao-Dong Shu, Hui-Qin Li, Yi Sun, Han Shan, Xi-Yang Sun, Ren-Hong Du, Ming Lu, Ming Xiao, Jian-Hua Ding, Gang Hu |
Journal | CNS neuroscience & therapeutics
(CNS Neurosci Ther)
Vol. 22
Issue 9
Pg. 729-39
(09 2016)
ISSN: 1755-5949 [Electronic] England |
PMID | 27306494
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | © 2016 John Wiley & Sons Ltd. |
Chemical References |
- Culture Media, Conditioned
- Cytokines
- Enzyme Inhibitors
- Ginkgolides
- Lactones
- Lipopolysaccharides
- Nerve Tissue Proteins
- ginkgolide B
- Glucose
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Topics |
- Animals
- Brain Edema
(drug therapy, etiology)
- Cell Hypoxia
(drug effects)
- Cell Polarity
(drug effects)
- Cells, Cultured
- Cerebral Cortex
(cytology)
- Culture Media, Conditioned
(pharmacology)
- Cytokines
(genetics, metabolism)
- Disease Models, Animal
- Enzyme Inhibitors
(pharmacology)
- Gene Expression Regulation
(drug effects)
- Ginkgolides
(pharmacology, therapeutic use)
- Glucose
(deficiency)
- Infarction, Middle Cerebral Artery
(drug therapy, pathology)
- Lactones
(pharmacology, therapeutic use)
- Lipopolysaccharides
(pharmacology)
- Male
- Mice
- Mice, Inbred C57BL
- Microglia
(drug effects)
- Motor Activity
(drug effects)
- Nerve Tissue Proteins
(genetics, metabolism)
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