Begeot M, Morel G, Rivest R W, Aubert M L, Dubois M P, Dubois P M
Neuroendocrinology. 1984 Mar;38(3):217-25. doi: 10.1159/000123894.
The influence of gonadoliberin (GnRH) on the differentiation of rat gonadotrophs in early fetal life was studied both in vivo and in vitro by immunocytology with anti-porcine luteinizing hormone beta (pLH beta) serum. Adenohypophysial primordia explanted from 11 to 13 days of gestation were maintained in organ culture in synthetic Parker's 199 medium enriched with insulin (0.5 microgram/ml) and transferrin (5 micrograms/ml). Cultures lasted to approximate the usual gestation period (21 days). Synthetic GnRH (10(-9) or 10(-12) M) was added to the culture medium during the first day of culture only. In contrast to a previous report, immunoreactive cells were detected in the primordia explanted either at 11 or 12 days of gestation only when cultured in the presence of GnRH. The appearance of positive localization was seen by 17 days. No differences due to GnRH dosage were observed in the mean cytoplasmic area of the cells in the different experimental groups as seen at the equivalent of 21 days. GnRH was not effective in a medium deprived of insulin. GnRH, added 6 h before the end of the culture, could also release the secretory product of gonadotrophs which recently developed the presence of immunoreactive pLH beta material. In these conditions, GnRH was shown to enter the cells as observed by immunocytochemistry on sections obtained after cryoultramicrotomy. Endogenous GnRH was also detected by the same technique in fetal pituitary glands removed from 14 to 21 days of gestation. It was always localized in agranular cells and from 18 days in some granular cells considered as gonadotrophs.(ABSTRACT TRUNCATED AT 250 WORDS)
采用抗猪促黄体生成素β(pLHβ)血清免疫细胞化学方法,在体内和体外研究了促性腺激素释放激素(GnRH)对大鼠胎儿早期促性腺激素细胞分化的影响。将妊娠11至13天的腺垂体原基在添加胰岛素(0.5微克/毫升)和转铁蛋白(5微克/毫升)的合成帕克199培养基中进行器官培养。培养持续至接近正常妊娠期(21天)。仅在培养的第一天向培养基中添加合成GnRH(10⁻⁹或10⁻¹²摩尔/升)。与先前的报道相反,仅在GnRH存在的情况下培养时,仅在妊娠11天或12天取出的原基中检测到免疫反应性细胞。到17天时可见阳性定位的出现。在相当于21天时,不同实验组细胞的平均细胞质面积未观察到因GnRH剂量而产生的差异。在缺乏胰岛素的培养基中,GnRH无效。在培养结束前6小时添加GnRH,也能释放最近出现免疫反应性pLHβ物质的促性腺激素细胞的分泌产物。在这些条件下,通过冷冻超薄切片后获得的切片免疫细胞化学观察表明,GnRH可进入细胞。用相同技术在妊娠14至21天取出的胎儿垂体中也检测到内源性GnRH。它总是定位于无颗粒细胞中,从18天起在一些被认为是促性腺激素细胞的颗粒细胞中也有定位。(摘要截短于250字)