Robblee L S, Shepro D, Belamarich F A
J Gen Physiol. 1973 Apr;61(4):462-81. doi: 10.1085/jgp.61.4.462.
A platelet subcellular fraction, sedimenting between 14,000 and 40,000 g and consisting primarily of membrane vesicles, accumulates up to 200-400 nmoles calcium/mg protein in the presence of ATP and oxalate. Steady-state levels of calcium accumulation are attained in 40-60 min. Calcium uptake requires adenosine triphosphate (ATP), is enhanced by oxalate, and is accompanied by the release of inorganic phosphate. Calcium accumulation and phosphate release require magnesium and are inhibited by Salyrgan (10 microM) and adenosine diphosphate (ADP) (1 mM), but not by ouabain (0.1 mM). The ATPase activity is stimulated by low concentrations of calcium (5-10 microM) and is inhibited by 2 mM EGTA. Electron microscopic histochemistry using lead nitrate to precipitate released phosphate results in lead precipitates localized primarily at the inner surface of membrane vesicles. These results provide evidence for a membrane ATPase that is stimulated by low concentrations of calcium and may be involved in the transport of calcium across the membrane. It is postulated that the observed calcium uptake activity is an in vitro manifestation of a calcium extrusion pump in the intact platelet.
一种血小板亚细胞组分,沉降系数在14,000至40,000克之间,主要由膜囊泡组成,在ATP和草酸盐存在的情况下,每毫克蛋白质可积累高达200 - 400纳摩尔的钙。钙积累的稳态水平在40 - 60分钟内达到。钙摄取需要三磷酸腺苷(ATP),草酸盐可增强其摄取,同时伴有无机磷酸盐的释放。钙积累和磷酸盐释放需要镁,并受到汞撒利(10微摩尔)和二磷酸腺苷(ADP)(1毫摩尔)的抑制,但不受哇巴因(0.1毫摩尔)的抑制。ATP酶活性受到低浓度钙(5 - 10微摩尔)的刺激,并被2毫摩尔乙二醇双四乙酸(EGTA)抑制。使用硝酸铅沉淀释放的磷酸盐的电子显微镜组织化学显示,铅沉淀主要位于膜囊泡的内表面。这些结果为一种受低浓度钙刺激且可能参与钙跨膜转运的膜ATP酶提供了证据。据推测,观察到的钙摄取活性是完整血小板中钙外排泵的体外表现。