首页> 外文期刊>Cellular Signalling >Interleukin-2 (IL-2) recepter-beta gamma signalling is activated by c-Kit in the absence of IL-2, or by exogenous IL-2 via JAK3/STAT5 in human papillomavirus-associated cervical cancer
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Interleukin-2 (IL-2) recepter-beta gamma signalling is activated by c-Kit in the absence of IL-2, or by exogenous IL-2 via JAK3/STAT5 in human papillomavirus-associated cervical cancer

机译:在不存在IL-2的情况下,c-Kit激活白介素2(IL-2)受体βγ信号传导,或者在人乳头瘤病毒相关宫颈癌中通过JAK3 / STAT5通过外源性IL-2激活IL-2。

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摘要

Activation of the interleukin-2 receptor (IL-2R) induces signalling cascades promoting T cell proliferation. However, signal transduction pathways triggered in IL-2R-expressing solid tumours are unknown. This report shows that human papillomavirus (HPV)-associated cervical cancer cells express an IL-2R composed of beta and gamma chains (IL-2Rbetagamma), and that IL-2-mediated activation increases the phosphorylation of JAK3 and STAT5, stimulating cell proliferation. Interestingly, endogenous IL-2 is not produced by these cells, suggesting the activation of IL-2R by an alternative mechanism. Accordingly, we found that Stem Cell Factor (SCF)-activated c-Kit induces phosphorylation of the IL-2Rbeta chain in the absence of IL-2. Moreover, inhibition of IL-2R phosphorylation by blocking c-Kit tyrosine kinase activity abolishes both, IL-2 and SCF-mediated proliferation. Thus, these results demonstrate that IL-2 triggers a JAK3/STAT5 cascade in HPV-associated cervical cancer cells expressing IL-2Rbetagamma, and that this receptor can be alternatively activated by SCF-activated c-Kit in the absence of IL-2. (C) 2004 Elsevier Inc. All rights reserved.
机译:白细胞介素2受体(IL-2R)的激活诱导促进T细胞增殖的信号级联反应。然而,在表达IL-2R的实体瘤中触发的信号转导途径尚不清楚。该报告表明,与人乳头瘤病毒(HPV)相关的宫颈癌细胞表达由β和γ链(IL-2Rbetagamma)组成的IL-2R,并且IL-2介导的激活增加了JAK3和STAT5的磷酸化,从而刺激细胞增殖。 。有趣的是,这些细胞未产生内源性IL-2,这表明IL-2R是通过其他机制激活的。因此,我们发现在没有IL-2的情况下,干细胞因子(SCF)激活的c-Kit诱导了IL-2Rbeta链的磷酸化。此外,通过阻断c-Kit酪氨酸激酶活性来抑制IL-2R磷酸化消除了IL-2和SCF介导的增殖。因此,这些结果证明IL-2在表达IL-2Rβγ的HPV相关宫颈癌细胞中触发JAK3 / STAT5级联,并且该受体可以在不存在IL-2的情况下被SCF激活的c-Kit激活。 (C)2004 Elsevier Inc.保留所有权利。

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