Rabkin S W
Department of Medicine, University Hospital (Shaughnessy), University of British Columbia, Vancouver, Canada.
Basic Res Cardiol. 1988 Nov-Dec;83(6):664-71. doi: 10.1007/BF01906961.
The effect of increases in extracellular calcium [Ca]o and the calcium ionophore A23187 on choline uptake and phosphatidylcholine biosynthesis was assessed in isolated cardiac myocytes. The cells were obtained from 7-day old chick embryos and were maintained in culture. Choline uptake was examined using [methyl 3H] choline. A23187 was found to increase choline uptake through the saturable choline uptake process. Pulse chase experiments using [methyl 3H] choline showed that after a 2 h incubation with choline, about 85% of the label was recovered in phosphocholine with most of the rest in phospholipid and a small amount in CDP-choline and glycerol phosphocholine. Increases in [Ca]o up to 10 mM did not affect the amount of label in phosphocholine or phospholipid, the rate of disappearance of label from phosphocholine, or the rate of appearance of labelled choline in phospholipid. In contrast, A23187, at concentrations up to 10(-4) M, was associated with a significant (p less than 0.05) increase in choline in the phosphocholine and phospholipid pool compared to control cells. The time course of the disappearance of choline from the phosphocholine pool and appearance in phospholipid pool was not significantly different between control cells and those treated with A23187. A23187 increased choline uptake via the specific uptake process. The effect on choline uptake may be attributed to the action of A23187 to facilitate the release of calcium from specific intracellular calcium storage sites rather than a nonspecific increase in [Ca]i that may have resulted from the increase in [Ca]o.
在分离的心肌细胞中评估了细胞外钙浓度([Ca]o)升高和钙离子载体A23187对胆碱摄取及磷脂酰胆碱生物合成的影响。细胞取自7日龄鸡胚并进行培养。使用[甲基-3H]胆碱检测胆碱摄取。发现A23187可通过可饱和的胆碱摄取过程增加胆碱摄取。使用[甲基-3H]胆碱进行的脉冲追踪实验表明,与胆碱孵育2小时后,约85%的标记物在磷酸胆碱中回收,其余大部分在磷脂中,少量在CDP-胆碱和甘油磷酸胆碱中。[Ca]o升高至10 mM并不影响磷酸胆碱或磷脂中的标记物含量、磷酸胆碱中标记物的消失速率或磷脂中标记胆碱的出现速率。相比之下,与对照细胞相比,浓度高达10^(-4) M的A23187可使磷酸胆碱和磷脂池中的胆碱显著增加(p<0.05)。对照细胞与用A23187处理的细胞之间,胆碱从磷酸胆碱池消失并出现在磷脂池中的时间进程无显著差异。A23187通过特异性摄取过程增加胆碱摄取。对胆碱摄取的影响可能归因于A23187促进从特定细胞内钙储存位点释放钙的作用,而非[Ca]o升高可能导致的[Ca]i非特异性增加。