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首页> 外文期刊>American Journal of Physiology >ATP stimulation of Na+/Ca2+ exchange in cardiac sarcolemmal vesicles.
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ATP stimulation of Na+/Ca2+ exchange in cardiac sarcolemmal vesicles.

机译:ATP刺激心肌肌膜囊泡中Na + / Ca2 +交换。

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摘要

In cardiac sarcolemmal vesicles, MgATP stimulates Na+/Ca2+ exchange with the following characteristics: 1) increases 10-fold the apparent affinity for cytosolic Ca2+; 2) a Michaelis constant for ATP of approximately 500 microM; 3) requires micromolar vanadate while millimolar concentrations are inhibitory; 4) not observed in the presence of 20 microM eosin alone but reinstated when vanadate is added; 5) mimicked by adenosine 5'-O-(3-thiotriphosphate), without the need for vanadate, but not by beta,gamma-methyleneadenosine 5'-triphosphate; and 6) not affected by unspecific protein alkaline phosphatase but abolished by a phosphatidylinositol-specific phospholipase C (PI-PLC). The PI-PLC effect is counteracted by phosphatidylinositol. In addition, in the absence of ATP, L-alpha-phosphatidylinositol 4,5-bisphosphate (PIP2) was able to stimulate the exchanger activity in vesicles pretreated with PI-PLC. This MgATP stimulation is not related to phosphorylation of the carrier, whereas phosphorylation appeared in the phosphoinositides, mainly PIP2, that coimmunoprecipitate with the exchanger. Vesicles incubated with MgATP and no Ca2+ show a marked synthesis of L-alpha-phosphatidylinositol 4-monophosphate (PIP) with little production of PIP2; in the presence of 1 microM Ca2+, the net synthesis of PIP is smaller, whereas that of PIP2 increases ninefold. These results indicate that PIP2 is involved in the MgATP stimulation of the cardiac Na+/Ca2+ exchanger through a fast phosphorylation chain: a Ca(2+)-independent PIP formation followed by a Ca(2+)-dependent synthesis of PIP2.
机译:在心脏肌膜囊泡中,MgATP刺激Na + / Ca2 +交换,其具有以下特征:1)对细胞质Ca2 +的表观亲和力增加10倍; 2)ATP的米氏常数约为500 microM; 3)在抑制毫摩尔浓度时需要微摩尔钒酸盐; 4)单独存在20 microM曙红时未观察到,但加入钒酸盐后可恢复; 5)由腺苷5'-O-(3-硫代三磷酸)模拟,不需要钒酸盐,但由β,γ-亚甲基腺苷5'-三磷酸模拟; 6)不受非特异性蛋白质碱性磷酸酶的影响,但被磷脂酰肌醇特异性磷脂酶C(PI-PLC)废除。 PI-PLC的作用被磷脂酰肌醇抵消。另外,在不存在ATP的情况下,L-α-磷脂酰肌醇4,5-双磷酸酯(PIP2)能够刺激用PI-PLC预处理的囊泡中的交换子活性。这种MgATP刺激与载体的磷酸化无关,而磷酸化出现在与交换剂共免疫沉淀的磷酸肌醇(主要是PIP2)中。用MgATP孵育且没有Ca2 +的囊泡显示L-α-磷脂酰肌醇4-单磷酸酯(PIP)的合成明显,几乎不产生PIP2。在存在1 microM Ca2 +的情况下,PIP的净合成量较小,而PIP2的净合成量增加了9倍。这些结果表明,PIP2通过快速磷酸化链参与心脏Na + / Ca2 +交换子的MgATP刺激:Ca(2+)依赖性PIP形成,然后是Ca(2+)依赖性PIP2合成。

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