Gylfe E
Department of Medical Cell Biology, Uppsala University, Sweden.
J Biol Chem. 1988 Sep 25;263(27):13750-4.
The cytoplasmic calcium concentration (Ca2+i) was measured in suspensions of fura-2 loaded mouse pancreatic beta-cells by continuously recording the 340/380 nm fluorescence excitation ratio. When the glucose concentration was raised from 3 to 20 mM, there was an initial lowering of Ca2+i followed by a sustained increase. Whereas the reduction in Ca2+i was related to the extracellular glucose concentration in a hyperbolic manner, the increasing component exhibited a sigmoidal dose-response relationship. Both effects became maximal at 15-20 mM of the sugar. Qualitatively similar bimodal Ca2+i responses were obtained with 30 mM mannose, 2 mM alpha-ketoisocaproic acid, 10 mM leucine, and 10 mM metabolism-stimulating leucine analogue beta-2-aminobicyclo-(2,2,1)-heptane-2-carboxylic acid. Fructose (30 mM) had virtually no effect on Ca2+i in the presence of extracellular Ca2+, and 10 mM arginine induced only a rise. The results indicate that nutrient secretagogues stimulate both the entry of Ca2+ into the beta-cells and its elimination from the cytoplasm by processes like organelle sequestration and outward transport. Consequently, the Ca2+i level determining insulin secretion results from the balance between two opposing actions.
通过连续记录340/380nm荧光激发比,在负载fura-2的小鼠胰腺β细胞悬液中测量细胞质钙浓度(Ca2+i)。当葡萄糖浓度从3mM提高到20mM时,Ca2+i首先降低,随后持续升高。Ca2+i的降低与细胞外葡萄糖浓度呈双曲线关系,而升高部分呈现S形剂量反应关系。两种效应在15-20mM的糖浓度下达到最大。用30mM甘露糖、2mMα-酮异己酸、10mM亮氨酸和10mM代谢刺激亮氨酸类似物β-2-氨基双环-(2,2,1)-庚烷-2-羧酸可获得定性相似的双峰Ca2+i反应。在细胞外Ca2+存在的情况下,30mM果糖对Ca2+i几乎没有影响,10mM精氨酸仅引起升高。结果表明,营养促分泌剂通过细胞器隔离和向外转运等过程,既刺激Ca2+进入β细胞,也刺激其从细胞质中清除。因此,决定胰岛素分泌的Ca2+i水平是由两种相反作用之间的平衡产生的。