Rorsman P, Berggren P O, Gylfe E, Hellman B
Biosci Rep. 1983 Oct;3(10):939-46. doi: 10.1007/BF01140663.
The cytosolic Ca2+ activity of insulin-releasing clonal cells (RINm5F) was studied with the intracellular fluorescent indicator quin-2. When the extracellular Ca2+ concentration was 1 mM, the basal cytosolic Ca2+ activity was 101 +/- 5 nM. Depolarization with 25 mM K+ increased this Ca2+ activity to at least 318 nM, an effect completely reversed by the voltage-dependent channel blocker D-600. In the presence of K+ alone these channels appeared to have a half-life of 6.7 +/- 0.8 min. In contrast to the action of K+, exposure of the RINm5F cells to 4 mM glucose resulted in a reduction of the cytosolic Ca2+ activity. This effect was observed during K+ depolarization but was more pronounced under basal conditions when it amounted to 20%. The data provide the first direct evidence that glucose can decrease the cytosolic Ca2+ activity in beta-cells. Unlike the case in normal beta-cells the glucose effect on the voltage-dependent Ca2+ channels in the RINm5F cells is apparently not sufficient to overcome the intracellular buffering of Ca2+. A defective depolarization is therefore a probable cause of the failing insulin secretion of RINm5F cells exposed to glucose.
利用细胞内荧光指示剂喹啉-2研究了胰岛素释放克隆细胞(RINm5F)的胞质Ca2+活性。当细胞外Ca2+浓度为1 mM时,基础胞质Ca2+活性为101±5 nM。用25 mM K+进行去极化可使该Ca2+活性增加至至少318 nM,电压依赖性通道阻滞剂D-600可完全逆转这一效应。仅在存在K+的情况下,这些通道的半衰期似乎为6.7±0.8分钟。与K+的作用相反,将RINm5F细胞暴露于4 mM葡萄糖会导致胞质Ca2+活性降低。在K+去极化过程中观察到了这种效应,但在基础条件下更为明显,此时降低幅度达20%。这些数据首次直接证明葡萄糖可降低β细胞中的胞质Ca2+活性。与正常β细胞不同,葡萄糖对RINm5F细胞中电压依赖性Ca2+通道的作用显然不足以克服Ca2+的细胞内缓冲作用。因此,去极化缺陷可能是暴露于葡萄糖的RINm5F细胞胰岛素分泌失败的原因。