Department of Molecular Biology, Cellular Biology, and Biochemistry, Brown University, Providence, RI 02912, USA.
Cell Calcium. 2013 Jan;53(1):16-23. doi: 10.1016/j.ceca.2012.11.011. Epub 2012 Dec 5.
Calcium signaling in cells directs diverse physiological processes. The calcium waves triggered by fertilization is a highly conserved calcium signaling event essential for egg activation, and has been documented in every egg tested. This activity is one of the few highly conserved events of egg activation through the course of evolution. Echinoderm eggs, as well as many other cell types, have three main intracellular Ca(2+) mobilizing messengers - IP3, cADPR and NAADP. Both cADPR and NAADP were identified as Ca(2+) mobilizing messengers using the sea urchin egg homogenate, and this experimental system, along with the intact urchin and starfish oocyte/egg, continues to be a vital tool for investigating the mechanism of action of calcium signals. While many of the major regulatory steps of the IP3 pathway are well resolved, both cADPR and NAADP remain understudied in terms of our understanding of the fundamental process of egg activation at fertilization. Recently, NAADP has been shown to trigger Ca(2+) release from acidic vesicles, separately from the ER, and a new class of calcium channels, the two-pore channels (TPCs), was identified as the likely targets for this messenger. Moreover, it was found that both cADPR and NAADP can be synthesized by the same family of enzymes, the ADP-rybosyl cyclases (ARCs). In this context of increasing amount of information, the potential coupling and functional roles of different messengers, intracellular stores and channels in the formation of the fertilization calcium wave in echinoderms will be critically evaluated.
细胞中的钙信号传导指导着多种生理过程。受精引发的钙波是一种高度保守的钙信号事件,对卵子激活至关重要,并且在经过测试的每一个卵子中都有记录。这种活性是卵子激活过程中经过进化高度保守的事件之一。棘皮动物卵子以及许多其他细胞类型都有三种主要的细胞内 Ca(2+)动员信使——IP3、cADPR 和 NAADP。cADPR 和 NAADP 都是使用海胆卵匀浆被鉴定为 Ca(2+)动员信使的,这个实验系统,以及完整的海胆和海星卵/卵子,仍然是研究钙信号作用机制的重要工具。虽然 IP3 途径的许多主要调节步骤已经得到很好的解决,但 cADPR 和 NAADP 在受精时卵子激活的基本过程的理解方面仍研究不足。最近,已经表明 NAADP 可以从 ER 以外的酸性小泡中触发 Ca(2+)释放,并且已经鉴定出一类新的钙通道,即双孔通道(TPCs),作为该信使的可能靶标。此外,发现 cADPR 和 NAADP 可以由同一类酶,即 ADP-核糖基环化酶(ARCs)合成。在信息量不断增加的情况下,棘皮动物受精钙波形成中不同信使、细胞内储存库和通道的潜在偶联和功能作用将受到严格评估。