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在单个大鼠肝细胞中,由ADP和ATP诱导的胞质游离Ca2+振荡对佛波酯的应用表现出不同的敏感性。

Oscillations in cytosolic free Ca2+ induced by ADP and ATP in single rat hepatocytes display differential sensitivity to application of phorbol ester.

作者信息

Dixon C J, Cobbold P H, Green A K

机构信息

Department of Human Anatomy and Cell Biology, University of Liverpool, U.K.

出版信息

Biochem J. 1995 Jul 1;309 ( Pt 1)(Pt 1):145-9. doi: 10.1042/bj3090145.

DOI:10.1042/bj3090145
PMID:7619050
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1135812/
Abstract

We have previously described differences in the oscillatory responses of cytosolic free Ca2+ concentration ([Ca2+]i) in hepatocytes to ADP and ATP, which we have interpreted as evidence that these two nucleotides are acting at distinct receptors. We show here that ADP- and ATP-induced oscillations are differentially sensitive to application of the phorbol ester 4 beta-phorbol 12,13-dibutyrate (PDB). ADP-induced [Ca2+]i oscillations are abolished by low concentrations of PDB (5-10 nM), whereas ATP-induced oscillations of long duration are refractory to PDB, even at greatly elevated concentrations (100 nM). The data illustrate a further difference in the actions of ADP and ATP, strengthening the argument that these agonists are not acting at the same receptor on rat hepatocytes.

摘要

我们之前曾描述过肝细胞中胞质游离钙离子浓度([Ca2+]i)对ADP和ATP的振荡反应存在差异,我们将此解释为这两种核苷酸作用于不同受体的证据。我们在此表明,ADP和ATP诱导的振荡对佛波酯4β-佛波醇12,13-二丁酸酯(PDB)的应用具有不同的敏感性。低浓度的PDB(5 - 10 nM)可消除ADP诱导的[Ca2+]i振荡,而ATP诱导的长时间振荡对PDB不敏感,即使在浓度大幅升高(100 nM)时也是如此。这些数据说明了ADP和ATP作用的进一步差异,强化了这些激动剂并非作用于大鼠肝细胞同一受体的观点。

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本文引用的文献

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Sinusoidal oscillations in intracellular calcium requiring negative feedback by protein kinase C.细胞内钙的正弦振荡需要蛋白激酶C的负反馈。
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Characterization of the effects of adenosine 5'-[beta-thio]-diphosphate in rat liver.5'-[β-硫代]-二磷酸腺苷对大鼠肝脏作用的特征研究
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Adenosine 5'-[alpha beta-methylene]triphosphate potentiates the oscillatory cytosolic Ca2+ responses of hepatocytes to ATP, but not to ADP.腺苷5'-[αβ-亚甲基]三磷酸增强肝细胞对ATP而非ADP的振荡性胞质Ca2+反应。
Biochem J. 1993 Aug 1;293 ( Pt 3)(Pt 3):757-60. doi: 10.1042/bj2930757.
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Increases in intracellular calcium via activation of an endogenous P2-purinoceptor in cultured CHO-K1 cells.通过激活培养的CHO-K1细胞中的内源性P2嘌呤受体增加细胞内钙含量。
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