Leduque P, Aratan-Spire S, Czernichow P, Dubois P M
J Clin Invest. 1986 Oct;78(4):1028-34. doi: 10.1172/JCI112657.
The ontogenesis of pancreatic thyrotropin-releasing hormone (TRH) in the human fetal gland was studied by radioimmunoassay or immunocytochemistry. The highest TRH concentrations (1,508.5 +/- 382.3 pg/mg wet wt) were detected between 6 and 8 wk of gestation. From 9 to 12 wk, TRH declined to 365.2 +/- 127.4 pg/mg wet wt and remained low thereafter (96.1 +/- 28.9 pg/mg wet wt). The immunocytochemical procedure was performed on semithin and thin sections from 12- to 19-wk-old human fetuses. At the light microscope level, TRH was found interspersed among the islet cell clusters (12 wk), and later (16 wk) inside the typical islets of Langerhans. Consecutive semithin sections treated by TRH and insulin antisera showed the same immunoreactive cells. Electron microscopy showed TRH in B cell secretory granules. These results are consistent with an eventual implication of TRH in the endocrine regulation of metabolism or in the fetal development of pancreas.
通过放射免疫分析或免疫细胞化学方法研究了人胎儿胰腺中促甲状腺激素释放激素(TRH)的个体发生。在妊娠6至8周时检测到最高的TRH浓度(1,508.5 +/- 382.3 pg/mg湿重)。从9至12周,TRH降至365.2 +/- 127.4 pg/mg湿重,此后保持在低水平(96.1 +/- 28.9 pg/mg湿重)。对12至19周龄人胎儿的半薄切片和超薄切片进行了免疫细胞化学操作。在光学显微镜水平,发现TRH散布在胰岛细胞簇之间(12周),之后(16周)在典型的胰岛内。用TRH和胰岛素抗血清处理的连续半薄切片显示相同的免疫反应性细胞。电子显微镜显示B细胞分泌颗粒中有TRH。这些结果与TRH最终参与代谢的内分泌调节或胰腺的胎儿发育一致。