Avdonin P V, Hayes B A, Popov E G, Tkachuk V A, Ryan U S
Department of Medicine, University of Miami School of Medicine, Florida 33101.
Tissue Cell. 1989;21(2):171-8. doi: 10.1016/0040-8166(89)90061-x.
The regulation of free cytoplasmic calcium concentration ([Ca2+]i) was studied in bovine pulmonary artery endothelial cells (BPAEC). The cells were seeded on the inner surface of glass cuvettes, grown to confluency and loaded with INDO-1. Using a multiwavelength method for estimation of [Ca2+]i it was shown that in Ca2+ containing medium a rapid rise of [Ca2+]i occurs in response to bradykinin, ATP or thrombin followed by a much slower decrease in free cytoplasmic calcium. Binding of extracellular Ca2+ by EGTA lowered basal [Ca2+]i but had no effect on the rate of agonist-induced [Ca2+]i increase or its absolute amount. In contrast, the kinetics of [Ca2+]i decrease were entirely different. A rapid (less than 0.5 min) decrease in [Ca2+]i to the basal level was observed immediately after the maximum had been achieved. If excess Ca2+ was added to the medium after EGTA, a second [Ca2+]i rise in response to the agonists occurred. The decrease in [Ca2+]i after the second peak was several times slower than the decrease in Ca2+ free medium. It is concluded that Ca2+ entry from the external medium had no effect on the maximal increase in [Ca2+]i but provides a severalfold increase in the duration the endothelial cell responses to the agonists.
研究了牛肺动脉内皮细胞(BPAEC)中游离细胞质钙浓度([Ca2+]i)的调节。将细胞接种在玻璃比色皿的内表面,生长至汇合后用INDO-1进行负载。使用多波长方法估算[Ca2+]i,结果表明,在含Ca2+的培养基中,缓激肽、ATP或凝血酶会导致[Ca2+]i迅速升高,随后游离细胞质钙的下降则慢得多。EGTA对细胞外Ca2+的结合降低了基础[Ca2+]i,但对激动剂诱导的[Ca2+]i升高速率或其绝对量没有影响。相反,[Ca2+]i下降的动力学则完全不同。在达到最大值后,立即观察到[Ca2+]i迅速(不到0.5分钟)下降至基础水平。如果在EGTA后向培养基中添加过量Ca2+,则会出现第二次激动剂诱导的[Ca2+]i升高。第二个峰值后[Ca2+]i的下降比无Ca2+培养基中的下降慢几倍。结论是,细胞外培养基中的Ca2+内流对[Ca2+]i的最大升高没有影响,但可使内皮细胞对激动剂的反应持续时间增加几倍。