Section on Cellular Signaling, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA.
CAPES Foundation, Ministry of Education of Brazil, Brasília, Brazil.
Thyroid. 2021 May;31(5):850-858. doi: 10.1089/thy.2020.0222. Epub 2021 Jan 12.
Thyrotropin (TSH) is well known as the hormone of the anterior pituitary thyrotrophs responsible for acting in the thyroid gland, where it stimulates synthesis and release of thyroid hormones through G and G protein coupled TSH receptors (TSHRs). In this study, we examined whether the functional TSHRs are also expressed in cultured rat pituitary cells, using double immunocytochemistry, quantitative reverse transcription-polymerase chain reaction analysis, cAMP and hormone measurements, and single-cell calcium imaging. Double immunocytochemistry revealed the expression of TSHRs in cultured corticotrophs and melanotrophs, in addition to previously identified receptors in folliculostellate cells. The functional coupling of these receptors to the G signaling pathway was not observed, as demonstrated by the lack of TSH activation of IP-dependent calcium mobilization in these cells when bathed in calcium-deficient medium. However, TSH increased cAMP production in a time- and concentration-dependent manner and facilitated calcium influx in single corticotrophs and melanotrophs, indicating their coupling to the G signaling pathway. Consistent with these findings, TSH stimulated adrenocorticotropin and β-endorphin release in male and female pituitary cells in a time- and concentration-dependent manner without affecting the expression of proopiomelanocortin gene. These results indicate that TSH is a potential paracrine modulator of anterior pituitary corticotrophs and melanotrophs, controlling the exocytotic but not the transcriptional pathway in a cAMP/calcium influx-dependent manner.
促甲状腺激素(TSH)是脑垂体前叶甲状腺细胞所分泌的激素,作用于甲状腺,通过 G 和 G 蛋白偶联的 TSH 受体(TSHRs)刺激甲状腺激素的合成和释放。在这项研究中,我们使用双重免疫细胞化学、定量逆转录聚合酶链反应分析、cAMP 和激素测量以及单细胞钙成像,检查了培养的大鼠垂体细胞中是否表达功能性 TSHR。双重免疫细胞化学显示 TSHR 除了在滤泡星状细胞中已鉴定的受体外,还表达在培养的促肾上腺皮质激素细胞和黑色素细胞中。这些受体与 G 信号通路的功能偶联未被观察到,因为在缺乏钙的培养基中,这些细胞中缺乏 TSH 激活 IP 依赖性钙动员证明了这一点。然而,TSH 以时间和浓度依赖的方式增加 cAMP 的产生,并促进单个促肾上腺皮质激素细胞和黑色素细胞中钙内流,表明它们与 G 信号通路偶联。这些发现与 TSH 以时间和浓度依赖的方式刺激雄性和雌性垂体细胞中促肾上腺皮质激素和β-内啡肽释放的结果一致,而不影响前阿黑皮素原基因的表达。这些结果表明,TSH 是一种潜在的垂体前叶促肾上腺皮质激素细胞和黑色素细胞的旁分泌调节剂,以 cAMP/钙内流依赖的方式控制细胞外排但不控制转录途径。