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人类胎儿星形胶质细胞和小胶质细胞中刺激诱导型趋化因子mRNA积累的不同模式。

Distinct patterns of stimulus-inducible chemokine mRNA accumulation in human fetal astrocytes and microglia.

作者信息

Hua L L, Lee S C

机构信息

Department of Pathology, Albert Einstein College of Medicine, Bronx, New York 10461, USA.

出版信息

Glia. 2000 Mar;30(1):74-81. doi: 10.1002/(sici)1098-1136(200003)30:1<74::aid-glia8>3.0.co;2-c.

Abstract

Interferon-gamma-inducible 10 kd protein (IP-10) is an ELR (Glu-Leu-Arg)(-) alpha chemokine with known chemotactic effects on T cells and monocytes, as well as anti-viral, anti-angiogenic, and anti-tumor effects. Previous studies have demonstrated that in cultured rat astrocytes and microglia, stimulation with LPS or virus can induce the expression of IP-10. In this study, we determined the pattern of IP-10 gene induction in primary human microglia and astrocytes by cytokines and LPS using ribonuclease protection assay. The expression of IP-10 mRNA was compared with that of other alpha (IL-8) and beta chemokines. The results showed that in human microglia, IP-10 expression was induced equally potently by LPS, IFNbeta or IFNgamma. "Proinflammatory" cytokines IL-1beta or TNFalpha also induced small amounts of IP-10 mRNA. "Anti-inflammatory" cytokines IL-4, IL-10 and TGFbeta were ineffective in inducing IP-10 in microglia. In human astrocytes, induction of IP-10 mRNA by cytokines was similar to that in microglia. LPS, however, was ineffective in inducing IP-10 in human astrocytes. The monocyte chemoattractant beta-chemokine I-309 mRNA was induced in human astrocytes and microglia by IFNbeta or IFNgamma, or by LPS in microglia, showing a tight co-regulation with IP-10 mRNA expression. In contrast to the potent induction of IP-10 and I-309 by IFNs in human glia, the ELR(+) alpha chemokine IL-8 mRNA was induced by IL-1beta and TNFalpha, and to a lesser extent by IFNbeta in microglia. IFNbeta but not IFNgamma was effective in inducing the expression of beta chemokines MIP-1alpha and MIP-1beta in human microglia, with the levels of mRNA similar to those induced by IL-1beta or TNFalpha. Neither MIP-1alpha nor MIP-1beta mRNAs were induced by any stimulation in human astrocytes. The induction of RANTES mRNA in microglia by IFNbeta, IL-1beta or TNFalpha was variable, showing no to low level expression depending on the case, whereas LPS provided a consistent inducing signal. In astrocytes, only cytokine combinations (IFN + IL-1beta) effectively induced the RANTES mRNA. These results demonstrate that distinct sets of chemokine genes are induced in human glial cells by cytokines and interferons. These results may have wide implications for inflammatory, vascular and neoplastic diseases of the CNS.

摘要

γ干扰素诱导的10kd蛋白(IP-10)是一种ELR(谷氨酸-亮氨酸-精氨酸)阴性的α趋化因子,对T细胞和单核细胞具有已知的趋化作用,以及抗病毒、抗血管生成和抗肿瘤作用。先前的研究表明,在培养的大鼠星形胶质细胞和小胶质细胞中,用脂多糖(LPS)或病毒刺激可诱导IP-10的表达。在本研究中,我们使用核糖核酸酶保护试验,通过细胞因子和LPS测定原代人小胶质细胞和星形胶质细胞中IP-10基因的诱导模式。将IP-10 mRNA的表达与其他α(IL-8)和β趋化因子的表达进行比较。结果显示,在人小胶质细胞中,LPS、IFNβ或IFNγ均能有效诱导IP-10的表达。“促炎”细胞因子IL-1β或TNFα也能诱导少量的IP-10 mRNA。“抗炎”细胞因子IL-4、IL-10和TGFβ在小胶质细胞中诱导IP-10无效。在人星形胶质细胞中,细胞因子对IP-10 mRNA的诱导与小胶质细胞相似。然而,LPS在人星形胶质细胞中诱导IP-10无效。单核细胞趋化β趋化因子I-309 mRNA在人星形胶质细胞和小胶质细胞中由IFNβ或IFNγ诱导,或在小胶质细胞中由LPS诱导,显示与IP-10 mRNA表达紧密共调节。与IFN在人神经胶质细胞中强力诱导IP-10和I-309不同,ELR阳性α趋化因子IL-8 mRNA在小胶质细胞中由IL-1β和TNFα诱导,IFNβ诱导程度较小。IFNβ而非IFNγ在人小胶质细胞中有效诱导β趋化因子MIP-1α和MIP-1β的表达,mRNA水平与IL-1β或TNFα诱导的水平相似。在人星形胶质细胞中,任何刺激均未诱导MIP-1α和MIP-1β mRNA。IFNβ、IL-1β或TNFα对小胶质细胞中RANTES mRNA的诱导是可变的,根据情况显示无表达至低水平表达,而LPS提供一致的诱导信号。在星形胶质细胞中,只有细胞因子组合(IFN + IL-1β)有效诱导RANTES mRNA。这些结果表明,细胞因子和干扰素在人神经胶质细胞中诱导不同组的趋化因子基因。这些结果可能对中枢神经系统的炎症、血管和肿瘤性疾病具有广泛的意义。

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