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Cloning and characterization of IL-10-related T cell-derived inducible factor (IL-TIF), a novel cytokine structurally related to IL-10 and inducible by IL-9

机译:IL-10相关性T细胞衍生诱导因子(IL-TIF)的克隆与鉴定,IL-10是一种结构上与IL-10相关并可以被IL-9诱导的新型细胞因子

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摘要

IL-9 is a Th2 cytokine active on various cell types such as T and B lymphocytes, mast cells, and eosinophils, and potentially involved in allergy and asthma. To understand better the molecular mechanisms underlying the activity of this cytokine, we used a cDNA subtraction method to identify genes specifically induced by IL-9 in mouse T cells. One of the IL-9 regulated genes isolated by this approach turned out to encode a 180-amino acid long protein, including a potential signal peptide, and showing 22% amino acid identity with IL-10. This protein, designated IL-10-related T cell-derived inducible factor (IL-TIF), is induced by IL-9 in thymic lymphomas, T cells, and mast cells, and by lectins in freshly isolated splenocytes. Experiments concerning the mechanism regulating IL-TIF expression in T cells indicate that IL-9 induction is rapid (within 1 h), does not require protein synthesis, and depends on the activation of the Janus kinase (JAK)-STAT pathway. In vivo, constitutive expression of IL-TIF was detected by RT-PCR in thymus and brain, suggesting that the role of this new factor is not restricted to the immune system, Transfection of HEK293 cells with the IL-TIF cDNA resulted in the production of a glycosylated protein of about 25 kDa that was found to induce STAT activation in mesangial and neuronal cell lines. Further studies will have to address the possibility that some of the IL-9 activities may be mediated by IL-TIF.
机译:IL-9是一种Th2细胞因子,对多种细胞类型具有活性,例如T和B淋巴细胞,肥大细胞和嗜酸性粒细胞,并可能参与过敏和哮喘。为了更好地了解这种细胞因子的活性背后的分子机制,我们使用了一种cDNA减法方法来鉴定IL-9在小鼠T细胞中特异性诱导的基因。通过这种方法分离的IL-9调控基因之一被编码为180个氨基酸长的蛋白质,包括潜在的信号肽,并与IL-10表现出22%的氨基酸同一性。这种蛋白被称为IL-10相关的T细胞衍生诱导因子(IL-TIF),在胸腺淋巴瘤,T细胞和肥大细胞中被IL-9诱导,在新鲜分离的脾细胞中被凝集素诱导。关于调节T细胞中IL-TIF表达机制的实验表明,IL-9诱导迅速(在1小时内),不需要蛋白质合成,并且取决于Janus激酶(JAK)-STAT途径的激活。在体内,通过RT-PCR在胸腺和大脑中检测到IL-TIF的组成型表达,这表明该新因子的作用不仅限于免疫系统,用IL-TIF cDNA转染HEK293细胞可导致产生发现约25kDa的糖基化蛋白在肾小球膜和神经元细胞系中诱导STAT活化。进一步的研究将不得不解决某些IL-9活性可能由IL-TIF介导的可能性。

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