Wesslén N, Pipeleers D, Van de Winkel M, Rorsman P, Hellman B
Department of Medical Cell Biology, Biomedicum, University of Uppsala, Sweden.
Acta Physiol Scand. 1987 Oct;131(2):230-4. doi: 10.1111/j.1748-1716.1987.tb08231.x.
Rat pancreatic beta and alpha 2 cells were purified by autofluorescence-activated cell sorting and used for electrophysiological patch clamp studies and measurements of the initial uptake of 45Ca. Both beta and alpha 2 cells were electrically active, the action potentials of the latter cells also were detected in the absence of glucose. Furthermore, alpha 2 cells differed from beta cells in lacking a glucose-sensitive K+ channel with a single conductance of 50-60 pS (in symmetric 140 mM K+ solutions). The rate of Ca2+ entry into the alpha 2 cells was slower than that into the beta cells, being equivalent to 0.2 mmol, kg-1 dry wt min-1. Whereas raising the glucose concentration to 20 mM significantly increased the amount of Ca2+ entering the beta cells, the sugar was without effect on Ca2+ entry into the alpha 2 cells.
通过自发荧光激活细胞分选法纯化大鼠胰腺β细胞和α2细胞,并将其用于电生理膜片钳研究以及45Ca初始摄取量的测量。β细胞和α2细胞均具有电活性,在无葡萄糖的情况下也能检测到后者细胞的动作电位。此外,α2细胞与β细胞不同,缺乏单通道电导为50 - 60 pS的葡萄糖敏感钾通道(在对称的140 mM K+溶液中)。Ca2+进入α2细胞的速率比进入β细胞的速率慢,相当于0.2 mmol·kg-1干重·min-1。将葡萄糖浓度提高到20 mM时,进入β细胞的Ca2+量显著增加,而该糖类对Ca2+进入α2细胞没有影响。