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2-氨基乙氧基二苯硼酸盐(2-APB)可拮抗1,4,5-三磷酸肌醇诱导的钙释放,抑制钙泵,并对储存-操作性钙内流通道具有使用依赖性且作用缓慢可逆。

2-Aminoethoxydiphenyl borate (2-APB) antagonises inositol 1,4,5-trisphosphate-induced calcium release, inhibits calcium pumps and has a use-dependent and slowly reversible action on store-operated calcium entry channels.

作者信息

Peppiatt Claire M, Collins Tony J, Mackenzie Lauren, Conway Stuart J, Holmes Andrew B, Bootman Martin D, Berridge Michael J, Seo Jeong T, Roderick H Llewelyn

机构信息

Laboratory of Molecular Signalling, The Babraham Institute, Babraham, Cambridge CB2 4AT, UK.

出版信息

Cell Calcium. 2003 Jul;34(1):97-108. doi: 10.1016/s0143-4160(03)00026-5.

Abstract

The action of 2-aminoethoxydiphenyl borate (2-APB) on Ca(2+) signalling in HeLa cells and cardiac myocytes was investigated. Consistent with other studies, we found that superfusion of cells with 2-APB rapidly inhibited inositol 1,4,5-trisphosphate (InsP(3))-mediated Ca(2+) release and store-operated Ca(2+) entry (SOC). In addition to abrogating hormone-evoked Ca(2+) responses, 2-APB could antagonise Ca(2+) signals evoked by a membrane permeant InsP(3) ester. 2-APB also slowed the recovery of intracellular Ca(2+) signals consistent with an effect on Ca(2+) ATPases. The inhibitory action of 2-APB on InsP(3) receptors (InsP(3)Rs), SOC channels and Ca(2+) pumps persisted for several minutes after washout of the compound. Application of 2-APB to unstimulated cells had no effect on subsequent Ca(2+) responses suggesting that it has a use-dependent action. Mitochondria in cells treated with 2-APB showed a rapid and slowly reversible swelling. 2-APB did not cause the mitochondria to depolarise, but it reduced the extent of mitochondrial calcium uptake. Although 2-APB has been demonstrated not to affect voltage-operated Ca(2+) channels or ryanodine receptors, we found that it gave a concentration-dependent long-lasting inhibition of Ca(2+) signalling in electrically-stimulated cardiac myocytes, where InsP(3)Rs and SOC channels do not play a significant role. Our data suggest that 2-APB has multiple cellular targets, a use-dependent action, is difficult to reverse and may affect Ca(2+) signalling in cell types where InsP(3) and SOC are not active.

摘要

研究了2-氨基乙氧基二苯基硼酸酯(2-APB)对HeLa细胞和心肌细胞中Ca(2+)信号传导的作用。与其他研究一致,我们发现用2-APB对细胞进行灌流可迅速抑制肌醇1,4,5-三磷酸(InsP(3))介导的Ca(2+)释放和储存操纵性Ca(2+)内流(SOC)。除了消除激素诱发的Ca(2+)反应外,2-APB还可拮抗膜通透性InsP(3)酯诱发的Ca(2+)信号。2-APB还减缓了细胞内Ca(2+)信号的恢复,这与对Ca(2+)ATP酶的作用一致。在洗去该化合物后,2-APB对InsP(3)受体(InsP(3)Rs)、SOC通道和Ca(2+)泵的抑制作用持续了几分钟。将2-APB应用于未刺激的细胞对随后的Ca(2+)反应没有影响,这表明它具有使用依赖性作用。用2-APB处理的细胞中的线粒体显示出快速且缓慢可逆的肿胀。2-APB不会导致线粒体去极化,但会降低线粒体钙摄取的程度。尽管已证明2-APB不影响电压门控性Ca(2+)通道或兰尼碱受体,但我们发现它对电刺激的心肌细胞中的Ca(2+)信号传导产生浓度依赖性的持久抑制,而在这些细胞中InsP(3)Rs和SOC通道不起重要作用。我们的数据表明,2-APB具有多个细胞靶点,具有使用依赖性作用,难以逆转,并且可能影响InsP(3)和SOC不活跃的细胞类型中的Ca(2+)信号传导。

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