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本文引用的文献

1
Dual-FRET imaging of IP and Ca revealed Ca-induced IP production maintains long lasting Ca oscillations in fertilized mouse eggs.双荧光共振能量转移成像显示,IP 和 Ca 的相互作用导致 IP 产生,维持了受精小鼠卵中长时间的 Ca 振荡。
Sci Rep. 2019 Mar 18;9(1):4829. doi: 10.1038/s41598-019-40931-w.
2
The KN-93 Molecule Inhibits Calcium/Calmodulin-Dependent Protein Kinase II (CaMKII) Activity by Binding to Ca/CaM.KN-93 分子通过与 Ca/CaM 结合抑制钙/钙调蛋白依赖性蛋白激酶 II(CaMKII)活性。
J Mol Biol. 2019 Mar 29;431(7):1440-1459. doi: 10.1016/j.jmb.2019.02.001. Epub 2019 Feb 10.
3
Protein kinase C epsilon mediates the inhibition of angiotensin II on the slowly activating delayed-rectifier potassium current through channel phosphorylation.蛋白激酶 C ɛ 通过通道磷酸化介导血管紧张素 II 对缓慢激活延迟整流钾电流的抑制作用。
J Mol Cell Cardiol. 2018 Mar;116:165-174. doi: 10.1016/j.yjmcc.2018.02.010. Epub 2018 Feb 13.
4
Improvement of cardiomyocyte function by a novel pyrimidine-based CaMKII-inhibitor.新型嘧啶基 CaMKII 抑制剂改善心肌细胞功能。
J Mol Cell Cardiol. 2018 Feb;115:73-81. doi: 10.1016/j.yjmcc.2017.12.015. Epub 2017 Dec 30.
5
Proteomics of phosphorylation and protein dynamics during fertilization and meiotic exit in the egg.卵母细胞受精和减数分裂后期中磷酸化和蛋白质动态变化的蛋白质组学研究
Proc Natl Acad Sci U S A. 2017 Dec 12;114(50):E10838-E10847. doi: 10.1073/pnas.1709207114. Epub 2017 Nov 28.
6
Calcium and Excitation-Contraction Coupling in the Heart.心脏中的钙与兴奋-收缩偶联
Circ Res. 2017 Jul 7;121(2):181-195. doi: 10.1161/CIRCRESAHA.117.310230.
7
Molecular mechanism of activation-triggered subunit exchange in Ca(2+)/calmodulin-dependent protein kinase II.钙离子/钙调蛋白依赖的蛋白激酶 II 的激活触发亚基交换的分子机制。
Elife. 2016 Mar 7;5:e13405. doi: 10.7554/eLife.13405.
8
Long-Term Potentiation: From CaMKII to AMPA Receptor Trafficking.长时程增强:从钙/钙调蛋白依赖性蛋白激酶II到α-氨基-3-羟基-5-甲基-4-异恶唑丙酸受体转运
Annu Rev Physiol. 2016;78:351-65. doi: 10.1146/annurev-physiol-021014-071753.
9
Homozygous mutation of PLCZ1 leads to defective human oocyte activation and infertility that is not rescued by the WW-binding protein PAWP.磷脂酶Cζ1(PLCZ1)的纯合突变导致人类卵母细胞激活缺陷和不育,WW结合蛋白PAWP无法挽救这种情况。
Hum Mol Genet. 2016 Mar 1;25(5):878-91. doi: 10.1093/hmg/ddv617. Epub 2015 Dec 31.
10
Specificity of calcium/calmodulin-dependent protein kinases in mouse egg activation.小鼠卵母细胞激活中钙/钙调蛋白依赖性蛋白激酶的特异性
Cell Cycle. 2014;13(9):1482-8. doi: 10.4161/cc.28432. Epub 2014 Mar 11.

基于 FRET 的 CaMKII 活性传感器(FRESCA):评估活细胞中 Ca 振荡反应的 CaMKII 活性的有用工具。

FRET-based sensor for CaMKII activity (FRESCA): A useful tool for assessing CaMKII activity in response to Ca oscillations in live cells.

机构信息

Department of Veterinary and Animal Sciences, University of Massachusetts, Amherst, Massachusetts 01003.

Veterinary and Animal Sciences Graduate Program, University of Massachusetts, Amherst, Massachusetts 01003.

出版信息

J Biol Chem. 2019 Aug 2;294(31):11876-11891. doi: 10.1074/jbc.RA119.009235. Epub 2019 Jun 14.

DOI:10.1074/jbc.RA119.009235
PMID:31201271
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6682743/
Abstract

Ca oscillations and consequent Ca/calmodulin-dependent protein kinase II (CaMKII) activation are required for embryogenesis, as well as neuronal, immunological, and cardiac signaling. Fertilization directly results in Ca oscillations, but the resultant pattern of CaMKII activity remains largely unclear. To address this gap, we first employed the one existing biosensor for CaMKII activation. This sensor, Camui, comprises CaMKIIα and therefore solely reports on the activation of this CaMKII variant. Additionally, to detect the activity of all endogenous CaMKII variants simultaneously, we constructed a substrate-based sensor for CaMKII activity, FRESCA (T-based ensor for aMKII ctivity). To examine the differential responses of the Camui and FRESCA sensors, we used several approaches to stimulate Ca release in mouse eggs, including addition of phospholipase Cζ cRNA, which mimics natural fertilization. We found that the Camui response is delayed or terminates earlier than the FRESCA response. FRESCA enables assessment of endogenous CaMKII activity in real-time by both fertilization and artificial reagents, such as Sr, which also leads to CaMKII activation. FRESCA's broad utility will be important for optimizing artificial CaMKII activation for clinical use to manage infertility. Moreover, FRESCA provides a new view on CaMKII activity, and its application in additional biological systems may reveal new signaling paradigms in eggs, as well as in neurons, cardiomyocytes, immune cells, and other CaMKII-expressing cells.

摘要

钙离子振荡以及随之而来的钙/钙调蛋白依赖性蛋白激酶 II(CaMKII)激活对于胚胎发生以及神经元、免疫和心脏信号传导都是必需的。受精直接导致钙离子振荡,但 CaMKII 活性的结果模式在很大程度上仍不清楚。为了解决这一差距,我们首先使用了现有的 CaMKII 激活生物传感器。这个传感器 Camui 由 CaMKIIα 组成,因此仅报告这种 CaMKII 变体的激活情况。此外,为了同时检测所有内源性 CaMKII 变体的活性,我们构建了一个基于底物的 CaMKII 活性传感器,FRESCA(基于 T 的 CaMKII 活性传感器)。为了检查 Camui 和 FRESCA 传感器的差异反应,我们使用了几种方法在小鼠卵中刺激钙离子释放,包括添加磷脂酶 Cζ cRNA,它模拟自然受精。我们发现 Camui 反应比 FRESCA 反应延迟或更早终止。FRESCA 通过受精和人工试剂(如 Sr)实时评估内源性 CaMKII 活性,人工试剂也会导致 CaMKII 激活。FRESCA 的广泛应用对于优化人工 CaMKII 激活以用于临床治疗不孕不育症非常重要。此外,FRESCA 提供了 CaMKII 活性的新视角,其在其他生物系统中的应用可能会揭示卵子以及神经元、心肌细胞、免疫细胞和其他表达 CaMKII 的细胞中的新信号转导模式。