INSERM U 176, 1 Rue Camille-Saini-Saëns, Université de Bordeaux II, 33077 Bordeaux, France.
J Neuroendocrinol. 1990 Dec 1;2(6):815-23. doi: 10.1111/j.1365-2826.1990.tb00646.x.
Abstract Lactotrophs from lactating rats were separated by unit gravity sedimentation on a continuous density gradient of bovine serum albumin and were identified in two populations located in the light fractions (fractions 3-5) and in the heavy fractions (fractions 7-9) of the gradient. After 7 days in vitro, the effects on prolactin release of thyrotropin-releasing hormone (TRH) and dopamine before and after pretreatment with 17beta-estradiol were studied by a continuous perifusion system and reverse hemolytic plaque assay. Light fraction lactotrophs spontaneously released large quantities of prolactin (22 ng/ml/2 min/10(6) cells) and this basal release was markedly elevated (51 ng/ml/2 min/10(6) cells) by pretreatment with 17beta-estradiol (10(-8) M, 48 h), while the amount of intracellular prolactin remained stable. Mean hemolytic plaque area was increased in the same manner by 17beta-estradiol pretreatment but the number of cells and the percentage of plaque-forming cells were not changed. Perifusion of dopamine-containing medium (10(-7) M) almost completely blocked basal prolactin release from light fraction cells and this inhibition was markedly reduced by 17beta-estradiol pretreatment. TRH-containing medium (10(-7) M) weakly stimulated basal prolactin release (about 190% from basal) and this response was significantly enhanced (to about 300% of basal release) by 17beta-estradiol pretreatment. Both dopaminergic inhibition and TRH-stimulatory effects were dose-dependent and their half maximal effect values were not changed by 17beta-estradiol pretreatment. Secretion of prolactin evaluated at the single cell level by the reverse hemolytic plaque assay corroborated the results obtained from perifusion experiments. Lactotrophs from heavy fractions released small amounts of prolactin (12 ng/ml/2 min/10(6) cells) and neither this basal release nor the amount of intracellular prolactin were markedly modified by 17beta-estradiol pretreatment. As opposed to the light fraction cells, lactotrophs found in heavy fractions were very sensitive to TRH (10(-7) M) stimulation with maximal stimulation reaching ten times basal release, but were less sensitive to dopamine (10(-7) M), with an inhibition of only 40% basal prolactin liberation. Pretreatment of heavy fraction lactotrophs with 17beta-estradiol induced similar effects to those observed after pretreatment of light fraction cells: the stimulation by TRH was increased (from 11 times to 16 times) whereas the inhibition by dopamine was diminished (from 35% to 60%), but cell number and the percentage of prolactin-secreting cells remained unchanged. From the above results, we suggest that: 1) lactotrophs in the lactating rat pituitary can be divided into two major subpopulations with regard to cellular size and density, prolactin production and responsiveness to TRH and dopamine; 2) 17beta-estradiol pretreatment increases basal prolactin release from light fraction cells but does not affect basal prolactin release from heavy fraction cells in this way; 3) pretreatment with 17beta-estradiol enhances TRH stimulation and reduces dopaminergic inhibition of prolactin release from lactotrophs.
摘要 通过在牛血清白蛋白连续密度梯度上进行单位重力沉降,从哺乳期大鼠的催乳细胞中分离出来,并在梯度的轻馏分(第 3-5 馏分)和重馏分(第 7-9 馏分)中鉴定出两种群体。在体外培养 7 天后,通过连续灌注系统和反向溶血斑测定法研究了促甲状腺素释放激素(TRH)和多巴胺在 17β-雌二醇预处理前后对催乳素释放的影响。轻馏分催乳细胞自发释放大量催乳素(22ng/ml/2min/106细胞),这种基础释放通过 17β-雌二醇(10-8M,48h)预处理明显升高(51ng/ml/2min/106细胞),而细胞内催乳素的量保持稳定。同样,17β-雌二醇预处理以相同的方式增加平均溶血斑面积,但细胞数量和形成斑的细胞百分比没有变化。含有多巴胺的培养基(10-7M)几乎完全阻断了轻馏分细胞的基础催乳素释放,而 17β-雌二醇预处理显著降低了这种抑制作用。含有 TRH 的培养基(10-7M)微弱刺激基础催乳素释放(约基础的 190%),而 17β-雌二醇预处理显著增强(约基础释放的 300%)。多巴胺能抑制和 TRH 刺激作用均呈剂量依赖性,其半最大效应值不因 17β-雌二醇预处理而改变。通过反向溶血斑测定法在单细胞水平上评估的催乳素分泌,证实了从灌注实验中获得的结果。重馏分中的催乳细胞释放少量催乳素(12ng/ml/2min/106细胞),并且这种基础释放或细胞内催乳素的量均不因 17β-雌二醇预处理而明显改变。与轻馏分细胞相反,在重馏分中发现的催乳细胞对 TRH(10-7M)刺激非常敏感,最大刺激达到基础释放的十倍,但对多巴胺(10-7M)的敏感性较低,基础催乳素释放抑制仅为 40%。17β-雌二醇预处理重馏分中的催乳细胞诱导与轻馏分细胞预处理观察到的相似作用:TRH 的刺激增加(从 11 倍增加到 16 倍),而多巴胺的抑制减少(从 35%减少到 60%),但细胞数量和分泌催乳素的细胞百分比保持不变。根据上述结果,我们认为:1)哺乳期大鼠垂体中的催乳细胞可以根据细胞大小和密度、催乳素产生和对 TRH 和多巴胺的反应性分为两个主要亚群;2)17β-雌二醇预处理增加了轻馏分细胞的基础催乳素释放,但不会以这种方式影响重馏分细胞的基础催乳素释放;3)17β-雌二醇预处理增强了 TRH 刺激作用,并降低了催乳素释放的多巴胺能抑制作用。