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哺乳动物卵激活和胚胎发育中的钙信号传导:亚细胞定位的影响。

Calcium signaling in mammalian egg activation and embryo development: the influence of subcellular localization.

机构信息

Reproductive Medicine Group, Laboratory of Reproductive and Developmental Toxicology, National Institute of Environmental Health Sciences, National Institutes of Health, Research Triangle Park, North Carolina 27709, USA.

出版信息

Mol Reprod Dev. 2012 Nov;79(11):742-56. doi: 10.1002/mrd.22078. Epub 2012 Sep 28.

DOI:10.1002/mrd.22078
PMID:22888043
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3502661/
Abstract

Calcium (Ca(2+) ) signals drive the fundamental events surrounding fertilization and the activation of development in all species examined to date. Initial studies of Ca(2+) signaling at fertilization in marine animals were tightly linked to new discoveries of bioluminescent proteins and their use as fluorescent Ca(2+) sensors. Since that time, there has been rapid progress in our understanding of the key functions for Ca(2+) in many cell types and of the impact of cellular localization on Ca(2+) signaling pathways. In this review, which focuses on mammalian egg activation, we consider how Ca(2+) is regulated and stored at different stages of oocyte development and examine the functions of molecules that serve as both regulators of Ca(2+) release and effectors of Ca(2+) signals. We then summarize studies exploring how Ca(2+) directs downstream effectors mediating both egg activation and later signaling events required for successful preimplantation embryo development. Throughout this review, we focus attention on how localization of Ca(2+) signals influences downstream signaling events, and attempt to highlight gaps in our knowledge that are ripe for future research.

摘要

钙(Ca(2+))信号驱动着受精和所有已研究物种的发育激活的基本事件。在海洋动物受精过程中对 Ca(2+)信号的最初研究与生物发光蛋白的新发现及其作为荧光 Ca(2+)传感器的应用紧密相关。自那时以来,我们对 Ca(2+)在许多细胞类型中的关键功能以及细胞定位对 Ca(2+)信号通路的影响的理解取得了快速进展。在这篇重点关注哺乳动物卵激活的综述中,我们考虑了 Ca(2+)在卵母细胞发育的不同阶段是如何被调节和储存的,并研究了作为 Ca(2+)释放调节剂和 Ca(2+)信号效应物的分子的功能。然后,我们总结了探讨 Ca(2+)如何指导下游效应物的研究,这些效应物介导卵激活和随后的信号事件,对于成功的胚胎植入前发育是必需的。在整篇综述中,我们关注 Ca(2+)信号的定位如何影响下游信号事件,并试图突出我们知识中的空白点,这些空白点为未来的研究提供了契机。

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本文引用的文献

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Activation of the epithelial Na+ channel triggers prostaglandin E₂ release and production required for embryo implantation.上皮钠通道的激活触发了前列腺素 E₂ 的释放和胚胎植入所必需的产生。
Nat Med. 2012 Jul;18(7):1112-7. doi: 10.1038/nm.2771.
2
STIM1 is required for Ca2+ signaling during mammalian fertilization.STIM1 在哺乳动物受精过程中的 Ca2+ 信号转导中是必需的。
Dev Biol. 2012 Jul 15;367(2):154-62. doi: 10.1016/j.ydbio.2012.04.028. Epub 2012 May 4.
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Ovastacin, a cortical granule protease, cleaves ZP2 in the zona pellucida to prevent polyspermy.卵透明带蛋白 2 酶,是皮层颗粒中的一种蛋白酶,能够切割透明带中的 ZP2,从而阻止多精入卵。
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Small-conductance calcium-activated K(+) channels 3 (SK3) regulate blastocyst hatching by control of intracellular calcium concentration.小电导钙激活钾通道 3(SK3)通过控制细胞内钙离子浓度来调节囊胚孵化。
Hum Reprod. 2012 May;27(5):1421-30. doi: 10.1093/humrep/des060. Epub 2012 Mar 12.
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Calcium influx-mediated signaling is required for complete mouse egg activation.钙离子内流介导的信号转导对于完全激活小鼠卵子是必需的。
Proc Natl Acad Sci U S A. 2012 Mar 13;109(11):4169-74. doi: 10.1073/pnas.1112333109. Epub 2012 Feb 27.
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NLRP5 mediates mitochondrial function in mouse oocytes and embryos.NLRP5 介导小鼠卵母细胞和胚胎中的线粒体功能。
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PLCζ causes Ca(2+) oscillations in mouse eggs by targeting intracellular and not plasma membrane PI(4,5)P(2).PLCζ 通过靶向细胞内而不是质膜 PI(4,5)P(2) 引起小鼠卵子中的 Ca(2+) 振荡。
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