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甲状腺滤泡腔内的碘化甲状腺球蛋白通过TSH/TSHR信号通路调节TTF-1和PAX8的表达。

Iodinated TG in Thyroid Follicular Lumen Regulates TTF-1 and PAX8 Expression via TSH/TSHR Signaling Pathway.

作者信息

Huang Huibin, Shi Yaxiong, Liang Bo, Cai Huiyao, Cai Qingyan

机构信息

Department of Endocrinology, The Second Affiliated Hospital of Fujian Medical University, Quanzhou, Fujian 362000, P.R. China.

出版信息

J Cell Biochem. 2017 Oct;118(10):3444-3451. doi: 10.1002/jcb.26001. Epub 2017 May 30.

Abstract

Our previous study showed that highly iodinated thyroglobulin (TG) inhibited thyroid transcription factor-1 (TTF-1) and paired box gene 8 (PAX8) expression, but the potential mechanism remains unclear. In this study, we constructed a thyroid follicle model in vitro to mimic its natural physiological structure and explored how iodinated TG in the follicular lumen tuned TTF-1 and PAX8 expression. Our data showed that lowly iodinated TG enhanced PKA activity while upregulation of both TTF-1 and PAX8 expression; and that highly iodinated TG triggered PKC activity while suppression of TTF-1 and PAX8 expression. Further, PKA agonist alone could increase TTF-1 and PAX8 expression while PKC agonist decreased TTF-1 and PAX8 level. If blocking PLC-PKC pathway using PKC-specific inhibitor, highly iodinated TG significantly promoted the expressions of TTF-1 and PAX8, and similarly PKA-specific blocker moderately inhibited TTF-1 and PAX8 expression. And opposite tendencies of TTF1 and PAX8 aberrant expression were observed in the condition of low iodinated TG when blocking PLC-PKC and cAMP-PKA signaling pathways. Our results indicated that iodinated TG manipulated TTF-1 and PAX8 expression through PLC-PKC and cAMP-PKA pathways, and highly iodinated TG played inhibitory role via PLC-PKC pathway from the TTF1 and PAX8 perspective while low level of iodinated TG was an activator through cAMP-PKA pathway. Our findings proved that iodinated TG in thyroid follicular lumen regulated TTF-1 and PAX8 expression through thyroid stimulating hormone/thyroid stimulating hormone receptor (TSH/TSHR) mediated cAMP-PKA and PLC-PKC signaling pathways. J. Cell. Biochem. 118: 3444-3451, 2017. © 2017 Wiley Periodicals, Inc.

摘要

我们之前的研究表明,高碘化甲状腺球蛋白(TG)可抑制甲状腺转录因子1(TTF-1)和配对盒基因8(PAX8)的表达,但其潜在机制仍不清楚。在本研究中,我们构建了体外甲状腺滤泡模型以模拟其天然生理结构,并探究滤泡腔内碘化TG如何调节TTF-1和PAX8的表达。我们的数据表明,低碘化TG增强PKA活性,同时上调TTF-1和PAX8的表达;而高碘化TG触发PKC活性,并抑制TTF-1和PAX8的表达。此外,单独的PKA激动剂可增加TTF-1和PAX8的表达,而PKC激动剂则降低TTF-1和PAX8的水平。若使用PKC特异性抑制剂阻断PLC-PKC途径,高碘化TG可显著促进TTF-1和PAX8的表达,同样地,PKA特异性阻滞剂可适度抑制TTF-1和PAX8的表达。并且在阻断PLC-PKC和cAMP-PKA信号通路的情况下,低碘化TG条件下观察到TTF1和PAX8异常表达的相反趋势。我们的结果表明,碘化TG通过PLC-PKC和cAMP-PKA途径调控TTF-1和PAX8的表达,从TTF1和PAX8的角度来看,高碘化TG通过PLC-PKC途径发挥抑制作用,而低水平的碘化TG则通过cAMP-PKA途径起激活作用。我们的研究结果证明,甲状腺滤泡腔内的碘化TG通过促甲状腺激素/促甲状腺激素受体(TSH/TSHR)介导的cAMP-PKA和PLC-PKC信号通路调节TTF-1和PAX8的表达。《细胞生物化学杂志》118: 3444 - 3451, 2017。© 2017威利期刊公司

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