Genazzani A A, Mezna M, Summerhill R J, Galione A, Michelangeli F
Department of Pharmacology, University of Oxford, Mansfield Road, Oxford OX1 3QT, United Kingdom.
J Biol Chem. 1997 Mar 21;272(12):7669-75. doi: 10.1074/jbc.272.12.7669.
Three endogenous molecules have now been shown to release Ca2+ in the sea urchin egg: inositol trisphosphate (InsP3), cyclic adenosine 5'-diphosphate ribose (cADPR), and nicotinic acid adenine dinucleotide phosphate (NAADP), a derivative of NADP. While the mechanism through which the first two molecules are able to release Ca2+ is established and well characterized with InsP3 and cADPR-activating InsP3 and ryanodine receptors, respectively, the newly described NAADP has been shown to release Ca2+ via an entirely different mechanism. The most striking feature of this novel Ca2+ release mechanism is its inactivation, since subthreshold concentrations of NAADP are able to fully and irreversibly desensitize the channel. In the present study we have investigated the fast kinetics of activation and inactivation of NAADP-induced Ca2+ release. NAADP was found to release Ca2+ in a biphasic manner, and such release was preceded by a pronounced latent period, which was inversely dependent on concentration. Moreover, the kinetic features of NAADP-induced Ca2+ release were not altered by pretreatment with low concentrations of NAADP, although the extent of Ca2+ release was greatly affected. Our data suggest that the inactivation of NAADP-induced Ca2+ release is an all-or-none phenomenon, and while some receptors have been fully inactivated, those that remain sensitive to NAADP do so without any change in kinetic features.
现已证明,三种内源性分子可使海胆卵释放Ca2+:肌醇三磷酸(InsP3)、环腺苷5'-二磷酸核糖(cADPR)和烟酰胺腺嘌呤二核苷酸磷酸(NAADP,NADP的衍生物)。虽然前两种分子释放Ca2+的机制已明确,且分别通过InsP3和cADPR激活InsP3受体和兰尼碱受体得到了充分表征,但新发现的NAADP已被证明通过完全不同的机制释放Ca2+。这种新型Ca2+释放机制最显著的特征是其失活,因为阈下浓度的NAADP能够使通道完全且不可逆地脱敏。在本研究中,我们研究了NAADP诱导的Ca2+释放的快速激活和失活动力学。发现NAADP以双相方式释放Ca2+,且这种释放之前有一个明显的潜伏期,该潜伏期与浓度呈反比。此外,低浓度NAADP预处理并未改变NAADP诱导的Ca2+释放的动力学特征,尽管Ca2+释放的程度受到很大影响。我们的数据表明,NAADP诱导的Ca2+释放失活是一种全或无现象,虽然一些受体已完全失活,但那些对NAADP仍敏感的受体,其动力学特征没有任何变化。