Schröder D, Wegner U, Besch W, Zühlke H
Mol Cell Endocrinol. 1983 Oct;32(2-3):179-93. doi: 10.1016/0303-7207(83)90081-3.
Well-preserved pancreatic islet cell suspensions were prepared from islets of Langerhans of neonatal rats by gentle trypsin treatment. Within a culture period of 4-6 days the islet cells reaggregate spontaneously and form pseudo-islets of different size and of a variable insulin content. While the ratio of insulin to glucagon in isolated islets of Langerhans is constant (18 +/- 1.9), the hormone ratio of the pseudo-islets is strongly variable and increased, indicating an excess of insulin. Glucose enhancement from 1.5 mmoles/l to 15 mmoles/l results in a significant stimulation of (pro)insulin biosynthesis whereas insulin secretion of the pseudo-islets is only slightly increased. At high glucose concentration (15 mmoles/l) insulin secretion of the pseudo-islets can be potentiated (by a factor of 4.5 +/- 0.46) by 3-isobutyl-l-methylxanthine (IBMX). Compared with the initial islet cell suspension, the cell aggregation during pseudo-islet formation did not result in an enhanced secretory response on glucose stimulation.
通过温和的胰蛋白酶处理,从新生大鼠的胰岛中制备出保存良好的胰岛细胞悬液。在4至6天的培养期内,胰岛细胞会自发重新聚集,形成大小各异且胰岛素含量可变的假胰岛。虽然分离的朗格汉斯胰岛中胰岛素与胰高血糖素的比例是恒定的(18±1.9),但假胰岛的激素比例变化很大且升高,表明胰岛素过量。葡萄糖浓度从1.5毫摩尔/升增加到15毫摩尔/升会显著刺激(前)胰岛素生物合成,而假胰岛的胰岛素分泌仅略有增加。在高葡萄糖浓度(15毫摩尔/升)下,3-异丁基-1-甲基黄嘌呤(IBMX)可使假胰岛的胰岛素分泌增强(增强因子为4.5±0.46)。与初始的胰岛细胞悬液相比,假胰岛形成过程中的细胞聚集并未导致对葡萄糖刺激的分泌反应增强。