Celastrol Suppresses Morphological and Transcriptional Responses in Microglial Cells Upon Stimulation with Double-Stranded RNA

被引:30
作者
Nakamichi, Kazuo [1 ]
Kitani, Hiroshi [2 ]
Takayama-Ito, Mutsuyo [1 ]
Morimoto, Kinjiro [3 ]
Kurane, Ichiro [1 ]
Saijo, Masayuki [1 ]
机构
[1] Natl Inst Infect Dis, Dept Virol 1, Lab Neurovirol, Shinjuku Ku, Tokyo 1628640, Japan
[2] Natl Inst Agrobiol Sci, Transgen Anim Res Ctr, Ibaraki, Japan
[3] Yasuda Womens Univ, Fac Pharm, Hiroshima, Japan
关键词
activation; chemokine; cytokine; cytoskeleton; microglia; morphology; NF-KAPPA-B; SIGNALING PATHWAYS; NITRIC-OXIDE; ACTIVATION; RELEASE; VIRUS; EXPRESSION; DISEASE; SYSTEM; ACID;
D O I
10.3109/00207451003615763
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Despite the pivotal role of microglia in the immune system of the brain, a growing body of evidence suggests that excessive microglial activation provokes neuronal and glial damage, leading to neurodegenerative and neuroinflammatory disorders. Celastrol, a triterpene, is a potent anti-inflammatory and antioxidant compound derived from perennial creeping plants belonging to the Celastraceae family. In the current study, we have analyzed the effect of celastrol on morphological and transcriptional responses in microglial MG6 cells upon stimulation with double-stranded RNA, a strong activator of innate immune cells. In the presence of celastrol, morphological changes were inhibited in double-stranded RNA-stimulated microglia. It was also found that the treatment of microglia with celastrol led to a significant decrease in the double-stranded RNA-induced expression of proinflammatory cytokines and chemokines. These data demonstrate that celastrol inhibits morphological and transcriptional responses during microglial activation.
引用
收藏
页码:252 / 257
页数:6
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