Lasa Marina, Gil-Araujo Beatriz, Palafox Marta, Aranda Ana
Departamento de Bioquímica-Instituto de Investigaciones Biomédicas Alberto Sols, Universidad Autónoma de Madrid-Consejo Superior de Investigaciones Científicas, 28029 Madrid, Spain.
Mol Endocrinol. 2010 Feb;24(2):412-22. doi: 10.1210/me.2009-0298. Epub 2009 Dec 23.
Pituitary function has been shown to be regulated by an increasing number of factors, including cytokines and hormones, such as TNFalpha and T(3). Both the proinflammatory cytokine TNFalpha and T(3) have been suggested to be involved in the maintenance of tissue homeostasis in the anterior pituitary gland. In this report we show that T(3) negatively interferes with MAPK p38 and nuclear factor-kappaB (NF-kappaB) activation by TNFalpha in GH4C1 cells. Our data demonstrate that MAPK p38 is specifically activated upon exposure to TNFalpha and that T(3) abolishes this activation in a time-dependent manner by a mechanism that involves the induction of the MAPK phosphatase, DUSP1. Our data show that the pool of up-regulated DUSP1 by T(3) is mainly localized to the cytosol, and that TNFalpha does not affect this localization. On the other hand, we show that T(3) impairs the activation of the NF-kappaB pathway induced by TNFalpha, producing a significant decrease in NF-kappaB-dependent transcription, phosphorylation of IkappaBalpha, translocation of p65/NF-kappaB to the nucleus, and p65/NF-kappaB transactivation potential. Interestingly, the overexpression of DUSP1 inhibits the NF-kappaB activation achieved by either TNFalpha or ectopic expression of the upstream inducer of MAPK p38. Conversely, DUSP1 depletion abrogates the inhibitory effect of T(3) on the induction of NF-kappaB-dependent transcription by TNFalpha. Overall, our results indicate that T(3) antagonizes TNFalpha signaling in rat pituitary tumor cells through the induction of DUSP1.
垂体功能已被证明受越来越多的因素调节,包括细胞因子和激素,如肿瘤坏死因子α(TNFα)和三碘甲状腺原氨酸(T3)。促炎细胞因子TNFα和T3均被认为参与垂体前叶组织稳态的维持。在本报告中,我们表明T3在GH4C1细胞中对TNFα激活的丝裂原活化蛋白激酶p38(MAPK p38)和核因子κB(NF-κB)具有负干扰作用。我们的数据表明,暴露于TNFα时MAPK p38会被特异性激活,并且T3通过一种涉及诱导丝裂原活化蛋白磷酸酶DUSP1的机制,以时间依赖性方式消除这种激活。我们的数据显示,T3上调的DUSP1主要定位于细胞质中,且TNFα不影响这种定位。另一方面,我们表明T3损害TNFα诱导的NF-κB信号通路的激活,导致NF-κB依赖性转录、IκBα磷酸化、p65/NF-κB向细胞核的转位以及p65/NF-κB反式激活潜能显著降低。有趣的是,DUSP1的过表达抑制了TNFα或MAPK p38上游诱导剂的异位表达所实现的NF-κB激活。相反,DUSP1的缺失消除了T3对TNFα诱导的NF-κB依赖性转录的抑制作用。总体而言,我们的结果表明T3通过诱导DUSP1拮抗大鼠垂体肿瘤细胞中的TNFα信号传导。