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首页> 外文期刊>American Journal of Physiology >Calcium-dependent regulation of calcium efflux by the cardiac sodium/calcium exchanger.
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Calcium-dependent regulation of calcium efflux by the cardiac sodium/calcium exchanger.

机译:钙钠通过心脏钠/钙交换剂的钙依赖调节。

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Allosteric regulation by cytosolic Ca2+ of Na(+)/Ca2+ exchange activity in the Ca2+ efflux mode has received little attention because it has been technically difficult to distinguish between the roles of Ca2+ as allosteric activator and transport substrate. In this study, we used transfected Chinese hamster ovary cells to compare the Ca2+ efflux activities in nontransfected cells and in cells expressing either the wild-type exchanger or a mutant, Delta(241-680), that operates constitutively; i.e., its activity does not require allosteric Ca2+ activation. Expression of the wild-type exchanger did not significantly lower the cytosolic Ca2+ concentration ([Ca2+](i)) compared with nontransfected cells. During Ca2+ entry through store-operated Ca2+ channels, Ca2+ efflux by the wild-type exchanger became evident only after [Ca2+](i) approached 100-200 nM. A subsequent decline in [Ca2+](i) was observed, suggesting that the activation process was time dependent. In contrast, Ca2+ efflux activity was evident under all experimental conditions in cells expressing the constitutive exchanger mutant. After transient exposure to elevated [Ca2+](i), the wild-type exchanger behaved similarly to the constitutive mutant for tens of seconds after [Ca2+](i) had returned to resting levels. We conclude that Ca2+ efflux activity by the wild-type exchanger is allosterically activated by Ca2+, perhaps in a time-dependent manner, and that the activated state is briefly retained after the return of [Ca2+](i) to resting levels.
机译:在Ca2 +外排模式下,通过胞质Ca2 +的Na(+)/ Ca2 +交换活性进行的变构调节几乎没有引起注意,因为在技术上很难区分Ca2 +作为变构激活剂和转运底物的作用。在这项研究中,我们使用转染的中国仓鼠卵巢细胞来比较未转染的细胞和表达野生型交换子或组成型运行的突变体Delta(241-680)的细胞中Ca2 +外排活性。即,其活性不需要变构Ca 2+活化。与未转染的细胞相比,野生型交换子的表达并未显着降低胞浆中的Ca2 +浓度([Ca2 +](i))。在通过存储操作的Ca2 +通道进入Ca2 +的过程中,仅在[Ca2 +](i)接近100-200 nM后,野生型交换子的Ca2 +外排才变得明显。观察到[Ca2 +](i)随后下降,表明激活过程是时间依赖性的。相反,在所有实验条件下,表达组成型交换子突变体的细胞中Ca2 +外排活性是明显的。在短暂暴露于升高的[Ca2 +](i)之后,在[Ca2 +](i)恢复到静止水平后的数十秒钟,野生型交换子的行为类似于本构突变体。我们得出的结论是,野生型交换子的Ca2 +外排活性可能是由Ca2 +变构激活的,可能是时间依赖性的,并且在[Ca2 +](i)恢复到静止水平后短暂保留了激活状态。

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