Kinard T A, de Vries G, Sherman A, Satin L S
Departments of Pharmacology and Toxicology and Physiology, Medical College of Virginia, Virginia Commonwealth University, Richmond, Viginia 23298-0524 USA.
Biophys J. 1999 Mar;76(3):1423-35. doi: 10.1016/S0006-3495(99)77303-0.
Glucose triggers bursting activity in pancreatic islets, which mediates the Ca2+ uptake that triggers insulin secretion. Aside from the channel mechanism responsible for bursting, which remains unsettled, it is not clear whether bursting is an endogenous property of individual beta-cells or requires an electrically coupled islet. While many workers report stochastic firing or quasibursting in single cells, a few reports describe single-cell bursts much longer (minutes) than those of islets (15-60 s). We studied the behavior of single cells systematically to help resolve this issue. Perforated patch recordings were made from single mouse beta-cells or hamster insulinoma tumor cells in current clamp at 30-35 degrees C, using standard K+-rich pipette solution and external solutions containing 11.1 mM glucose. Dynamic clamp was used to apply artificial KATP and Ca2+ channel conductances to cells in current clamp to assess the role of Ca2+ and KATP channels in single cell firing. The electrical activity we observed in mouse beta-cells was heterogeneous, with three basic patterns encountered: 1) repetitive fast spiking; 2) fast spikes superimposed on brief (<5 s) plateaus; or 3) periodic plateaus of longer duration (10-20 s) with small spikes. Pattern 2 was most similar to islet bursting but was significantly faster. Burst plateaus lasting on the order of minutes were only observed when recordings were made from cell clusters. Adding gCa to cells increased the depolarizing drive of bursting and lengthened the plateaus, whereas adding gKATP hyperpolarized the cells and lengthened the silent phases. Adding gCa and gKATP together did not cancel out their individual effects but could induce robust bursts that resembled those of islets, and with increased period. These added currents had no slow components, indicating that the mechanisms of physiological bursting are likely to be endogenous to single beta-cells. It is unlikely that the fast bursting (class 2) was due to oscillations in gKATP because it persisted in 100 microM tolbutamide. The ability of small exogenous currents to modify beta-cell firing patterns supports the hypothesis that single cells contain the necessary mechanisms for bursting but often fail to exhibit this behavior because of heterogeneity of cell parameters.
葡萄糖可触发胰岛中的爆发性活动,这种活动介导了触发胰岛素分泌的Ca2+摄取。除了负责爆发的通道机制仍未明确外,尚不清楚爆发是单个β细胞的内在特性,还是需要电耦合的胰岛。虽然许多研究人员报告了单个细胞中的随机放电或准爆发,但也有一些报告描述了单个细胞的爆发持续时间(数分钟)比胰岛的爆发持续时间(15 - 60秒)长得多。我们系统地研究了单个细胞的行为,以帮助解决这个问题。在30 - 35摄氏度下,使用标准的富含K+的移液器溶液和含有11.1 mM葡萄糖的外部溶液,在电流钳模式下对单个小鼠β细胞或仓鼠胰岛素瘤肿瘤细胞进行穿孔膜片钳记录。动态钳用于向电流钳模式下的细胞施加人工KATP和Ca2+通道电导,以评估Ca2+和KATP通道在单个细胞放电中的作用。我们在小鼠β细胞中观察到的电活动是异质性的,遇到了三种基本模式:1)重复性快速放电;2)叠加在短暂(<5秒)平台期上的快速放电;或3)持续时间较长(10 - 20秒)且伴有小放电的周期性平台期。模式2与胰岛爆发最相似,但速度明显更快。只有从细胞簇进行记录时,才观察到持续数分钟的爆发平台期。向细胞中添加gCa会增加爆发的去极化驱动力并延长平台期,而添加gKATP会使细胞超极化并延长静息期。同时添加gCa和gKATP并不会抵消它们各自的作用,反而可以诱导出类似于胰岛的强烈爆发,且周期增加。这些添加的电流没有缓慢成分,表明生理性爆发的机制可能是单个β细胞内在的。快速爆发(第2类)不太可能是由于gKATP的振荡,因为在100 microM甲苯磺丁脲中它仍然持续存在。小的外源电流改变β细胞放电模式的能力支持了这样一种假设,即单个细胞包含爆发所需的机制,但由于细胞参数的异质性,它们常常无法表现出这种行为。