Herbert D C, Ishikawa H, Rennels E G
Endocrinology. 1979 Jan;104(1):97-100. doi: 10.1210/endo-104-1-97.
The cells from the 2B8 clonal strain of pituitary cells which previously have been reported to produce only PRL were incubated with varying amounts of ovine PRL (oPRL) ranging from 0.01--1000 ng/ml. After 1 h, significantly less PRL was measured in culture media from cells incubated with all doses of oPRL employed. This inhibition was dose related. The cells were rinsed five times with Hank's balanced salt solution and subsequently placed into PRL-free media for an additional hour. Hypersecretion of hormone occurred from those cells previously exposed to 1--1000 ng/ml oPRL. The PRL in the media from cells previously exposed to 0.01--0.1 ng/ml was similar to that in the control culture. In some experiments, the cellular concentration of PRL was determined at the end of each of the two 1-h incubation periods. After the initial exposure to oPRL, an increase in intracellular hormone was observed only in those groups incubated with 1--1000 ng/ml oPRL. In contrast, after the cells were rinsed and placed into PRL-free medium, the cellular concentration of PRL was unchanged in all groups except the group previously exposed to 100 ng/ml oPRL. These data indicate that PRL can inhibit its own secretion through direct action on the lactotrophs of the anterior pituitary gland.
先前报道仅产生催乳素(PRL)的垂体细胞2B8克隆株的细胞,与浓度范围为0.01 - 1000 ng/ml的不同量羊催乳素(oPRL)一起孵育。1小时后,在所使用的所有剂量oPRL孵育的细胞的培养基中测得的PRL显著减少。这种抑制作用与剂量相关。用汉克平衡盐溶液将细胞冲洗5次,随后放入无PRL的培养基中再孵育1小时。先前暴露于1 - 1000 ng/ml oPRL的那些细胞出现激素分泌过多的情况。先前暴露于0.01 - 0.1 ng/ml的细胞培养基中的PRL与对照培养物中的相似。在一些实验中,在两个1小时孵育期结束时测定细胞内PRL浓度。在最初暴露于oPRL后,仅在与1 - 1000 ng/ml oPRL孵育的那些组中观察到细胞内激素增加。相反,在细胞冲洗后放入无PRL培养基中,除先前暴露于100 ng/ml oPRL的组外,所有组的细胞内PRL浓度均未改变。这些数据表明PRL可通过直接作用于垂体前叶的催乳细胞来抑制其自身分泌。