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三磷酸腺苷(ATP)对心肌肌膜囊泡中钠/钙交换的刺激作用。

ATP stimulation of Na+/Ca2+ exchange in cardiac sarcolemmal vesicles.

作者信息

Berberián G, Hidalgo C, DiPolo R, Beaugé L

机构信息

Instituto de Investigación Médica Mercedes y Martín Ferreyra, Córdoba, Argentina.

出版信息

Am J Physiol. 1998 Mar;274(3):C724-33. doi: 10.1152/ajpcell.1998.274.3.C724.

Abstract

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.

摘要

在心肌肌膜囊泡中,MgATP刺激钠/钙交换,具有以下特点:1)将对胞质Ca2+的表观亲和力提高10倍;2)ATP的米氏常数约为500微摩尔;3)需要微摩尔浓度的钒酸盐,而毫摩尔浓度则具有抑制作用;4)单独存在20微摩尔曙红时未观察到,但添加钒酸盐后恢复;5)可被5'-O-(3-硫代三磷酸)腺苷模拟,无需钒酸盐,但不能被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影响,但被磷脂酰肌醇特异性磷脂酶C(PI-PLC)消除。PI-PLC的作用被磷脂酰肌醇抵消。此外,在没有ATP的情况下,L-α-磷脂酰肌醇4,5-二磷酸(PIP2)能够刺激经PI-PLC预处理的囊泡中的交换器活性。这种MgATP刺激与载体的磷酸化无关,而磷酸化出现在与交换器共免疫沉淀的磷酸肌醇中,主要是PIP2。用MgATP且无Ca2+孵育的囊泡显示出L-α-磷脂酰肌醇4-单磷酸(PIP)的显著合成,PIP2的产生很少;在存在1微摩尔Ca2+的情况下,PIP的净合成较小,而PIP2的净合成增加9倍。这些结果表明,PIP2通过快速磷酸化链参与MgATP对心脏钠/钙交换器的刺激:先是不依赖Ca(2+)的PIP形成,然后是依赖Ca(2+)的PIP2合成。

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