Buchan A M, Barber D L, Gregor M, Soll A H
Gastroenterology. 1987 Oct;93(4):791-800. doi: 10.1016/0016-5085(87)90442-2.
Enteroglucagon-containing cells have been maintained in short-term culture, and the morphologic characteristics of these cells and their response to selected agents have been determined. After 48 h in culture the ultrastructural appearance of the enteroglucagon-immunoreactive cells showed evidence of polarization with re-formation of apical microvilli and the secretory granules concentrated at the opposite pole of the cell. The size of the intracellular secretory granules was 370 +/- 15 nm. The release of enteroglucagonlike immunoreactivity was stimulated in a dose-dependent manner by the adrenergic agonists epinephrine and isoproterenol. The response to epinephrine was competitively inhibited by propranolol, producing a rightward shift of the dose-responsive curve. The alpha-adrenergic agonists methoxamine and clonidine did not stimulate enteroglucagon release above basal. The adenyl cyclase activator forskolin also stimulated release of the peptide in a dose-dependent manner. Carbachol and somatostatin produced a dose-dependent inhibition of epinephrine-stimulated release, indicating direct inhibitory modulation of enteroglucagonlike immunoreactive cells. Somatostatin also inhibited forskolin-stimulated release. These data indicate that canine ileal enteroglucagon cells in short-term culture respond to a number of specific stimuli.
含肠高血糖素的细胞已在短期培养中得以维持,并且已确定了这些细胞的形态学特征及其对选定试剂的反应。培养48小时后,肠高血糖素免疫反应性细胞的超微结构显示出极化迹象,顶端微绒毛重新形成,分泌颗粒集中在细胞的相对极。细胞内分泌颗粒的大小为370±15纳米。肾上腺素能激动剂肾上腺素和异丙肾上腺素以剂量依赖性方式刺激肠高血糖素样免疫反应性的释放。普萘洛尔竞争性抑制对肾上腺素的反应,使剂量反应曲线向右移动。α-肾上腺素能激动剂甲氧明和可乐定在基础水平之上未刺激肠高血糖素释放。腺苷酸环化酶激活剂福斯高林也以剂量依赖性方式刺激该肽的释放。卡巴胆碱和生长抑素对肾上腺素刺激的释放产生剂量依赖性抑制,表明对肠高血糖素样免疫反应性细胞有直接抑制调节作用。生长抑素也抑制福斯高林刺激的释放。这些数据表明,短期培养的犬回肠肠高血糖素细胞对多种特定刺激有反应。