Huang Huibin, Shi Yaxiong, Liang Bo, Cai Huiyao, Cai Qingyan
Department of Endocrinology, The Second Affiliated Hospital of Fujian Medical University, Quanzhou, Fujian 362000, P.R. China.
J Cell Biochem. 2017 Oct;118(10):3444-3451. doi: 10.1002/jcb.26001. Epub 2017 May 30.
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.
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