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褪黑素促进糖氧剥夺诱导的BV2小胶质细胞向M2极化

Melatonin promoted M2 polarization of BV2 microglia induced by glucose and oxygen deprivation
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摘要 目的:研究褪黑素处理对糖氧剥夺(OGD)诱导的小鼠小胶质细胞系BV2细胞功能的影响。方法:BV2细胞分为对照组(control)、氧糖剥夺组(OGD)和褪黑素处理组(OGD+Mel)。利用流式细胞仪检测各组细胞CD16/32和兔多克隆抗体CD206的表达,real time RT-PCR方法检测BV2细胞中iNOS和Arg-1 mRNA表达,利用酶联免疫吸附试验(ELISA)方法检测BV2细胞培养上清中IL-1β和IL-4的水平。结果:OGD诱导可促进BV2细胞向M1极化,表现为CD16/32上调、iNOS mRNA表达增加,培养上清中IL-1β水平升高;经过褪黑素处理后,CD16/32、iNOS mRNA,培养上清中IL-1β表达下降,CD206、Arg-1和IL-4表达增加。结论:OGD可诱导BV2细胞向M1方向分化,而褪黑素可使OGD诱导的BV2细胞向M2极化。 Objective:To study the effect of melatonin treatment on the function of mouse microglial cell line BV2 induced by glucose and oxygen deprivation(OGD).Methods:BV2 cells were divided into control group(control),oxygen and sugar deprivation group(OGD)and melatonin treatment group(OGD+Mel).Flow cytometry was used to detect the expression of CD16/32 and rabbit polyclonal antibody CD206.Real-time RT-PCR was used to detect the mRNA expression of iNOS and Arg-1 in BV2 cells.The levels of IL-1βand IL-4 in the supernatant of BV2 cell culture were determined by enzyme-linked immunosorbent assay(ELISA).Results:OGD could promote the polarization of BV2 cells towards M1,which showed that CD16/32 was up-regulated,iNOS mRNA expression was increased,and IL-1βlevel was increased in supernatant.After melatonin treatment,CD16/32,iNOS mRNA,IL-1βexpression in culture supernatant decreased,CD206,Arg-1,and IL-4 expression increased.Conclusion:Melatonin can promote M2 polarization of BV2 microglia induced by glucose and oxygen deprivation.
作者 张晓斌 潘鹏宇 邹正 董玉书 Zhang Xiaobin;Pan Pengyu;Zou Zheng;Dong Yushu(Institute of Neuroscience,General Hospital of Northern Theater Command Base,Shenyang 110016,China)
出处 《神经解剖学杂志》 CAS CSCD 2022年第2期214-218,共5页 Chinese Journal of Neuroanatomy
基金 国家自然科学基金(81971133,82071481)。
关键词 褪黑素 糖氧剥夺 M2极化 炎症 小胶质细胞 melatonin oxygen-glucose deprivation M2 polarization inflammation microglia
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  • 1Gordon S.Alternative activation of macrophages[J].Nat Rev Immunol,2003;3:23-35.
  • 2Mantovani A,Sozzani S,Locati M et al.Macrophage polarization:tumor-associated macrophages as a paradigm for polarized M2 mononuclear phagocytes[J].Trends Immunol,2002;23:549-555.
  • 3Ckless K,Lampert,A,Reiss J et al.Inhibition of arginase activity enhances inflammation in mice with allergic airway disease,in association with increases in protein S-nitrosylation and tyrosine nitration[J].J Immunol,2008;181:4255-4264.
  • 4Dai R,Phillips R A,Karpuzoglu E et al.Estrogen regulates transcription factors STAT-1 and NF-kappaB to promote inducible nitric oxide synthase and inflammatory responses[J].J Immunol,2009;183:6998-7005.
  • 5Kwon S J,Lee G T,Lee J H et al.Bone morphogenetic protein-6 induces the expression of inducible nitric oxide synthase in macrophages[J].Immunology,2009;128:e758-765.
  • 6Kleinert H,Schwarz P M,Forstermann U.Regulation of the expression of inducible nitric oxide synthase[J].Biol Chem,2003;384:1343-1364.
  • 7Porta C,Rimoldi M,Raes G et al.Tolerance and M2 (alternative) macrophage polarization are related processes orchestrated by p50 nuclear factor kappaB[J].Proc Natl Acad Sci USA,2009;106:14978-14983.
  • 8Davis R L,Sanchez A C,Lindley D J et al.Effects of mechanistically distinct NF-kappaB inhibitors on glial inducible nitric-oxide synthase expression[J].Nitric Oxide,2005;12:200-209.
  • 9Mizel S B,Honko A N,Moors M A et al.Induction of macrophage nitric oxide production by Gram-negative flagellin involves signaling via heteromeric Toll-like receptor 5/Toll-like receptor 4 complexes[J].J Immunol,2003;170:6217-6223.
  • 10Martinez F O,Helming L,Gordon S.Alternative activation of macrophag es:an immunologic functional perspective[J].Annu Rev Immunol,2009;27:451-483.

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