Nogami H, Yoshimura F, Carrillo A J, Sharp Z D, Sheridan P J
Endocrinol Jpn. 1985 Oct;32(5):625-34. doi: 10.1507/endocrj1954.32.625.
Adult male rats were injected with different doses (1, 10, and 100 micrograms) of 17 beta-estradiol daily for 5 days, and the changes in prolactin (PRL) mRNA levels were examined by in situ hybridization and cytoplasmic dot blot hybridization using cloned cDNA for rat prolactin mRNA. An increase in cytoplasmic PRL mRNA content was evident in all the animals treated with estrogen as revealed with cytoplasmic dot blot analysis. There were however, no significant differences in PRL mRNA content among the three estradiol treated groups. Cytoplasmic PRL mRNA was also demonstrated by in situ hybridization on the frozen pituitary sections using a 3H-labeled PRL cDNA probe. The number of grains per cell was increased after estrogen treatment. 3H-thymidine uptake into pituitary cells was also examined in vivo using combined techniques of immunocytochemistry and autoradiography. Although the percentage of immunoreactive PRL cells which took up thymidine in their nuclei increased to more than double after estrogen treatment, the increase in the total number of immunoreactive PRL cells was small. These results suggest that the major effect of estrogen on PRL cells is an increase in the accumulation of PRL mRNA in the individual PRL cells. The number of grains per cell was found to vary from cell to cell, both in control and estrogen treated animals. This variability is discussed in relation to the functional heterogeneity within the PRL cell population.
成年雄性大鼠每天注射不同剂量(1、10和100微克)的17β-雌二醇,持续5天,然后使用大鼠催乳素mRNA的克隆cDNA,通过原位杂交和细胞质斑点印迹杂交检测催乳素(PRL)mRNA水平的变化。细胞质斑点印迹分析显示,所有接受雌激素治疗的动物细胞质PRL mRNA含量均明显增加。然而,三个雌二醇治疗组之间的PRL mRNA含量没有显著差异。使用3H标记的PRL cDNA探针在冷冻的垂体切片上进行原位杂交,也证实了细胞质PRL mRNA的存在。雌激素处理后,每个细胞的银粒数增加。还使用免疫细胞化学和放射自显影相结合的技术在体内检测了垂体细胞对3H-胸腺嘧啶的摄取。尽管雌激素处理后,细胞核中摄取胸腺嘧啶的免疫反应性PRL细胞百分比增加到两倍以上,但免疫反应性PRL细胞总数的增加很小。这些结果表明,雌激素对PRL细胞的主要作用是增加单个PRL细胞中PRL mRNA的积累。在对照动物和雌激素处理的动物中,都发现每个细胞的银粒数因细胞而异。结合PRL细胞群体内的功能异质性对这种变异性进行了讨论。