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草莓切迹同源物2是一种新型炎症反应因子,主要但并非仅由中枢神经系统中的星形胶质细胞表达。

Strawberry notch homolog 2 is a novel inflammatory response factor predominantly but not exclusively expressed by astrocytes in the central nervous system.

作者信息

Grill Magdalena, Syme Taylor E, Noçon Aline L, Lu Andy Z X, Hancock Dale, Rose-John Stefan, Campbell Iain L

机构信息

School of Molecular Bioscience, University of Sydney, Sydney, Australia.

Institute of Experimental and Clinical Pharmacology, Medical University of Graz, Graz, Austria.

出版信息

Glia. 2015 Oct;63(10):1738-52. doi: 10.1002/glia.22841. Epub 2015 Apr 22.

DOI:10.1002/glia.22841
PMID:25903009
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4676294/
Abstract

Interleukin-6 (IL-6) participates in the host response to injury and infection in the central nervous system (CNS). We identified strawberry notch homolog 2 (Sbno2) as an IL-6-stimulated gene in murine astrocytes. Sbno2 is a mouse homolog of the sno gene in Drosophila but little is known about the regulation or function of the mammalian gene. Here we examined the regulation of the Sbno2 gene in astrocytes in vitro and in the murine CNS following systemic endotoxin administration. In murine and human cultured astrocytes, Sbno2 gene expression was significantly upregulated in a dose- and time-dependent fashion by hyper-IL-6 (IL-6 + soluble IL-6 receptor). The level of Sbno2 mRNA was also upregulated significantly in murine astrocytes by other glycoprotein130 cytokine-family members and the pro-inflammatory cytokines interleukin-1 beta and tumor necrosis factor alpha. These changes were reflected by corresponding alterations in the level of the SBNO2 protein. Inhibiting protein synthesis resulted in higher Sbno2 mRNA and did not abolish the upregulation of Sbno2 mRNA mediated by hyper-IL-6. Inhibition of transcription led to a rapid reduction in hyper-IL-6-induced Sbno2 mRNA in astrocytes suggesting that the Sbno2 mRNA is quite unstable. Following intra-peritoneal lipopolysaccharide injection in mice, Sbno2 mRNA levels in the brain were significantly increased. Cellular localization studies revealed that this increase in Sbno2 mRNA occurred predominantly in astrocytes and in the choroid plexus and in some microglia, endothelial cells, and neurons. These findings are consistent with SBNO2 functioning as an acute inflammatory response gene in astrocytes as well as other cells in the CNS.

摘要

白细胞介素-6(IL-6)参与中枢神经系统(CNS)对损伤和感染的宿主反应。我们将草莓缺口同源物2(Sbno2)鉴定为小鼠星形胶质细胞中IL-6刺激的基因。Sbno2是果蝇中sno基因的小鼠同源物,但对该哺乳动物基因的调控或功能知之甚少。在这里,我们研究了体外星形胶质细胞以及全身给予内毒素后小鼠中枢神经系统中Sbno2基因的调控情况。在小鼠和人类培养的星形胶质细胞中,超IL-6(IL-6 + 可溶性IL-6受体)以剂量和时间依赖性方式显著上调Sbno2基因表达。其他糖蛋白130细胞因子家族成员以及促炎细胞因子白细胞介素-1β和肿瘤坏死因子α也显著上调了小鼠星形胶质细胞中Sbno2 mRNA的水平。这些变化反映在SBNO2蛋白水平的相应改变上。抑制蛋白质合成导致Sbno2 mRNA水平升高,并且并未消除超IL-6介导的Sbno2 mRNA上调。转录抑制导致星形胶质细胞中超IL-6诱导的Sbno2 mRNA迅速减少,这表明Sbno​​2 mRNA相当不稳定。给小鼠腹腔注射脂多糖后,脑中Sbno2 mRNA水平显著增加。细胞定位研究表明,Sbno2 mRNA的这种增加主要发生在星形胶质细胞、脉络丛以及一些小胶质细胞、内皮细胞和神经元中。这些发现与SBNO2作为星形胶质细胞以及中枢神经系统中其他细胞的急性炎症反应基因发挥作用一致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cab2/4676294/be8f0cd40458/GLIA-63-1738-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cab2/4676294/920e7ce5a053/GLIA-63-1738-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cab2/4676294/4e412aad74d7/GLIA-63-1738-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cab2/4676294/8da0c7c558d0/GLIA-63-1738-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cab2/4676294/c58ee7a3307a/GLIA-63-1738-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cab2/4676294/c5321607b8ee/GLIA-63-1738-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cab2/4676294/4a4de11db58a/GLIA-63-1738-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cab2/4676294/be8f0cd40458/GLIA-63-1738-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cab2/4676294/920e7ce5a053/GLIA-63-1738-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cab2/4676294/9790d2cbfa40/GLIA-63-1738-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cab2/4676294/4e412aad74d7/GLIA-63-1738-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cab2/4676294/8da0c7c558d0/GLIA-63-1738-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cab2/4676294/c58ee7a3307a/GLIA-63-1738-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cab2/4676294/c5321607b8ee/GLIA-63-1738-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cab2/4676294/4a4de11db58a/GLIA-63-1738-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cab2/4676294/be8f0cd40458/GLIA-63-1738-g008.jpg

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