Lugo D I, Pintar J E
Department of Anatomy and Cell Biology, College of Physicians and Surgeons, Columbia University, New York, New York 10032, USA.
Dev Biol. 1996 Jan 10;173(1):110-8. doi: 10.1006/dbio.1996.0010.
Proopiomelanocortin (POMC)-producing cells comprise nearly 100% of the adult rat intermediate lobe (IL) hormone-producing cells. Secretion by these cells in the adult is primarily under negative regulation by dopamine. Although the POMC-derived peptide alpha-MSH has been detected in plasma of fetal rats, the secretory capability of fetal melanotrophs has not yet been examined directly. Here we have used the reverse hemolytic plaque assay to assess, at the single-cell level, basal and regulated release by melanotrophs from fetal and early postnatal ages. Basal secretion was detected at the earliest age examined [Embryonic Day 17.5 (e17.5)], but CRH (10(-8) M) stimulated secretion was not observed until e19.5. As development proceeded, CRH increased both individual plaque sizes and the percentage of melanotrophs stimulated to secrete. An unexpected, transient inhibition of CRH stimulated release from melanotrophs by dexamethasone (DEX, 10(-6) M) was observed from e19.5-p2 (postnatal Day 2). By p3, however, DEX no longer inhibited melanotroph secretion while inhibition of CRH-stimulated release from p3 corticotrophs was readily detected. The dopamine agonist ergocryptine (ERG, 10(-6) M) inhibited basal secretion from melanotrophs, but not corticotrophs, at all ages examined. Taken together, these results indicate that melanotrophs undergo a maturation process in which they are initially nonresponsive to CRH, next possess functional CRH and steroid receptors, and finally, undergo functional uncoupling of steroid receptors which characterizes the adult IL. The loss of steroid-mediated inhibition of stimulated secretion parallels the arrival of catecholaminergic input into the IL. In contrast, the early response of melanotrophs to dopaminergic agonists, which can be detected 1 week prior to arrival of catecholaminergic fibers into the neurointermediate lobe, appears to be an intrinsic feature of these cells that is never present in corticotrophs.
促阿黑皮素原(POMC)生成细胞几乎占成年大鼠中间叶(IL)激素生成细胞的100%。这些细胞在成年期的分泌主要受多巴胺的负调控。虽然在胎鼠血浆中已检测到POMC衍生肽α-促黑素(α-MSH),但胎鼠黑素细胞的分泌能力尚未直接检测。在此,我们使用反向溶血空斑试验在单细胞水平评估胎龄和出生后早期黑素细胞的基础分泌和调节分泌。在最早检测的年龄[胚胎第17.5天(e17.5)]就检测到基础分泌,但直到e19.5才观察到促肾上腺皮质激素释放激素(CRH,10⁻⁸ M)刺激的分泌。随着发育进行,CRH增加了单个空斑大小以及被刺激分泌的黑素细胞百分比。从e19.5到出生后第2天(p2)观察到地塞米松(DEX,10⁻⁶ M)对CRH刺激的黑素细胞释放有意外的短暂抑制作用。然而,到p3时,DEX不再抑制黑素细胞分泌,而对p3促肾上腺皮质激素细胞CRH刺激释放的抑制作用很容易检测到。多巴胺激动剂麦角隐亭(ERG,10⁻⁶ M)在所有检测年龄均抑制黑素细胞的基础分泌,但不抑制促肾上腺皮质激素细胞的基础分泌。综上所述,这些结果表明黑素细胞经历一个成熟过程,在此过程中它们最初对CRH无反应,接着拥有功能性CRH和类固醇受体,最后,类固醇受体发生功能性解偶联,这是成年IL的特征。类固醇介导的刺激分泌抑制作用的丧失与儿茶酚胺能输入到达IL平行。相反,黑素细胞对多巴胺能激动剂的早期反应,可在儿茶酚胺能纤维到达神经中间叶前1周检测到,这似乎是这些细胞的一个固有特征,而促肾上腺皮质激素细胞中从未有此特征。