Temporal and Spatial Dynamics of Astroglial Reaction and Immune Response in Cuprizone-Induced Demyelination

被引:0
作者
Jun An
Jun-Jun Yin
Yan He
Ruo-Xuan Sui
Qiang Miao
Qing Wang
Jie-Zhong Yu
Jing-Wen Yu
Fu-Dong Shi
Cun-Gen Ma
Bao-Guo Xiao
机构
[1] Shanxi University of Chinese Medicine,The Key Research Laboratory of Benefiting Qi for Acting Blood Circulation Method to Treat Multiple Sclerosis of State Administration of Traditional Chinese Medicine
[2] Shanxi Datong University,Institute of Brain Science
[3] Barrow Neurological Institute,Department of Neurology
[4] St. Joseph’s Hospital and Medical Center,Institute of Neurology, Huashan Hospital, Institutes of Brain Science and State Key Laboratory of Medical Neurobiology
[5] Fudan University,undefined
来源
Neurotoxicity Research | 2020年 / 37卷
关键词
CPZ-induced demyelination; Astroglial reaction; Immune response; Remyelination;
D O I
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学科分类号
摘要
The cuprizone (CPZ)-induced demyelination is a relatively reproducible animal model and has been extremely useful for identifying the specific cellular and molecular signals that regulate oligodendrocyte survival and efficiency of oligodendrogenesis and remyelination. Here, we reported the temporal and spatial dynamics of astroglial reaction and immune response in CPZ-induced demyelinating model. CPZ did not induce significant microglia and astrocyte reaction after 2 weeks of feeding. After 4–6 weeks of CPZ feeding, microglia and astrocytes were markedly migrated and accumulated in myelin sheath. Simultaneously, the expression of tight junction protein ZO-1 was declined and the infiltration of CD4+IFNγ+ and CD4+IL-17+ T cells was increased in the brain, accompanied by increased production of IFN-γ and IL-17 in the extract of brain. However, the levels of IFN-γ and IL-17 were reduced, while IL-6 and TNF-α were elevated in the supernatant of splenocytes. At the 4th and 6th weeks of feeding, CPZ caused astrocyte activation and upregulated the expression of BDNF, CNTF, and IGF-II, providing a neurotrophic microenvironment in the brain. At this stage, NG2+ and PDGF-Rα+ oligodendroglia progenitor cells were enhanced in the corpus callosum, but the myelin sheath is still severely lost. Therefore, targeting microglia to improve the inflammatory microenvironment should contribute to the remyelination.
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页码:587 / 601
页数:14
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