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甲状腺激素介导的细胞外信号调节激酶/双特异性磷酸酶1通路激活通过下调核因子-κB活性增强生长激素4C1细胞的凋亡。

Thyroid hormone-mediated activation of the ERK/dual specificity phosphatase 1 pathway augments the apoptosis of GH4C1 cells by down-regulating nuclear factor-kappaB activity.

作者信息

Chiloeches Antonio, Sánchez-Pacheco Aurora, Gil-Araujo Beatriz, Aranda Ana, Lasa Marina

机构信息

Departamento de Bioquímica y Biología Molecular, Facultad de Medicina, Universidad de Alcalá, Madrid, Spain.

出版信息

Mol Endocrinol. 2008 Nov;22(11):2466-80. doi: 10.1210/me.2008-0107. Epub 2008 Aug 28.

Abstract

Thyroid hormone (T3) plays a crucial role in processes such as cell proliferation and differentiation, whereas its implication on cellular apoptosis has not been well documented. Here we examined the effect of T3 on the apoptosis of GH4C1 pituitary cells and the mechanisms underlying this effect. We show that T3 produced a significant increase in apoptosis in serum-depleted conditions. This effect was accompanied by a decrease in nuclear factor-kappaB (NF-kappaB)-dependent transcription, IkappaBalpha phosphorylation, translocation of p65/NF-kappaB to the nucleus, phosphorylation, and transactivation. Moreover, these effects were correlated with a T3-induced decrease in the expression of antiapoptotic gene products, such as members of the inhibitor of apoptosis protein and Bcl-2 families. On the other hand, ERK but not c-Jun N-terminal kinase or MAPK p38, was activated upon exposure to T3, and inhibition of ERK alone abrogated T3-mediated apoptosis. In addition, T3 increased the expression of the MAPK phosphatase, dual specificity phosphatase 1 (DUSP1), in an ERK-dependent manner. Interestingly, the suppression of DUSP1 expression abrogated T3-induced inhibition of NF-kappaB-dependent transcription and p65/NF-kappaB translocation to the nucleus, as well as T3-mediated apoptosis. Overall, our results indicate that T3 induces apoptosis in rat pituitary tumor cells by down-regulating NF-kappaB activity through a mechanism dependent on the ERK/DUSP1 pathway.

摘要

甲状腺激素(T3)在细胞增殖和分化等过程中发挥着关键作用,而其对细胞凋亡的影响尚未得到充分记载。在此,我们研究了T3对GH4C1垂体细胞凋亡的影响及其潜在机制。我们发现,在血清缺乏的条件下,T3可显著增加细胞凋亡。这种效应伴随着核因子-κB(NF-κB)依赖性转录、IκBα磷酸化、p65/NF-κB向细胞核的转位、磷酸化及反式激活的减少。此外,这些效应与T3诱导的抗凋亡基因产物表达降低相关,如凋亡抑制蛋白家族和Bcl-2家族的成员。另一方面,暴露于T3时,细胞外信号调节激酶(ERK)被激活,而c-Jun氨基末端激酶或丝裂原活化蛋白激酶p38未被激活,单独抑制ERK可消除T3介导的细胞凋亡。此外,T3以ERK依赖性方式增加丝裂原活化蛋白激酶磷酸酶双特异性磷酸酶1(DUSP1)的表达。有趣的是,抑制DUSP1的表达可消除T3诱导的对NF-κB依赖性转录和p65/NF-κB向细胞核转位的抑制,以及T3介导的细胞凋亡。总体而言,我们的结果表明,T3通过依赖ERK/DUSP1途径的机制下调NF-κB活性,从而诱导大鼠垂体肿瘤细胞凋亡。

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