Oki S, Nakao K, Tanaka I, Kinoshita F, Naki Y, Imura H
Endocrinology. 1982 Aug;111(2):418-24. doi: 10.1210/endo-111-2-418.
gamma MSH, a putative hormone in the N-terminal region of the ACTH/beta-endorphin (beta-EP) precursor protein, was studied by RIA with an antiserum against gamma 3MSH in ACTH-producing mouse pituitary tumor cells, AtT-20/D16v. Serial dilution of the culture medium or the cell extract gave parallel lines to the standard curve in the RIA for gamma MSH. Rat median eminence extracts enhanced the release of gamma MSH-like immunoreactivity (gamma MSH-LI) concomitant with ACTH-like immunoreactivity (ACTH-LI) and beta-EP-like immunoreactivity (beta-EP-LI). Dexamethasone suppressed the release of gamma MSH-LI as well as ACTH-LI and beta-EP-LI. Gel exclusion chromatography of the culture medium and the cell extract has revealed that gamma MSH-LI consists of two peaks; one eluted near the elution position of beta-lipotropin and the other near the elution position of beta-EP. There was no peak corresponding to the elution position of synthetic gamma 3MSH. However, sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) has demonstrated that gamma MSH-LI migrated at five positions with molecular weights of 31K, 21-23K, 16-17K, 13-14K, and 3.8K, respectively. The 31K gamma MSH coincided with the migration position of 31K ACTH of 31K beta-EP, and 21-23K gamma MSH coincided with the position of 21-23K ACTH on SDS-PAGE. The 16-17K gamma MSH coincided with the mouse 16K fragment (reported by Eipper and Mains) of ACTH-beta-lipotropin precursor protein in the migration in SDS-PAGE and in immunoreactivity to anti-gamma MSH antiserum. [3H]Glucosamine was incorporated into 16K, 13K, and 3.8K gamma MSH. These results suggest that AtT-20/D16v cells produce gamma MSH-LIs with molecular weights of 31K, 21-23K, 16-17K, 13-14K, and 3.8K, and they are secreted concomitantly with ACTH-LI and beta-EP-LI.
γ促黑素是促肾上腺皮质激素/β-内啡肽(β-EP)前体蛋白N端区域的一种假定激素,我们用抗γ3促黑素的抗血清通过放射免疫分析法(RIA)在产生促肾上腺皮质激素的小鼠垂体瘤细胞AtT-20/D16v中对其进行了研究。培养基或细胞提取物的系列稀释在γ促黑素的放射免疫分析中与标准曲线呈平行线。大鼠正中隆起提取物增强了γ促黑素样免疫反应性(γMSH-LI)的释放,同时伴有促肾上腺皮质激素样免疫反应性(ACTH-LI)和β-EP样免疫反应性(β-EP-LI)。地塞米松抑制了γMSH-LI以及ACTH-LI和β-EP-LI的释放。对培养基和细胞提取物进行凝胶排阻色谱分析发现,γMSH-LI由两个峰组成;一个在β-促脂素的洗脱位置附近洗脱,另一个在β-EP的洗脱位置附近洗脱。没有与合成γ3促黑素的洗脱位置相对应的峰。然而,十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)表明,γMSH-LI在五个位置迁移,分子量分别为31K、21 - 23K、16 - 17K、13 - 14K和3.8K。31K的γ促黑素与31K促肾上腺皮质激素或31Kβ-EP的迁移位置一致,21 - 23K的γ促黑素与SDS-PAGE上21 - 23K促肾上腺皮质激素的位置一致。16 - 17K的γ促黑素在SDS-PAGE迁移以及对抗γ促黑素抗血清的免疫反应性方面与促肾上腺皮质激素-β-促脂素前体蛋白的小鼠16K片段(由Eipper和Mains报道)一致。[3H]氨基葡萄糖被掺入16K、13K和3.8K的γ促黑素中。这些结果表明,AtT-20/D16v细胞产生分子量为31K、21 - 23K、16 - 17K、13 - 14K和3.8K的γMSH-LI,并且它们与ACTH-LI和β-EP-LI一起分泌。