• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

核内钙离子信号转导。

Nuclear Ca(2+) signalling.

机构信息

Instituto de Biología y Genética Molecular (IBGM), Universidad de Valladolid y Consejo Superior de Investigaciones Científicas (CSIC), c/Sanz y Forés 3, 47003 Valladolid, Spain.

出版信息

Cell Calcium. 2011 May;49(5):280-9. doi: 10.1016/j.ceca.2010.11.004. Epub 2010 Dec 10.

DOI:10.1016/j.ceca.2010.11.004
PMID:21146212
Abstract

Ca(2+) signalling is important for controlling gene transcription. Changes of the cytosolic Ca(2+) (Ca(2+)) may promote migration of transcription factors or transcriptional regulators to the nucleus. Changes of the nucleoplasmic Ca(2+) (Ca(2+)) can also regulate directly gene expression. Ca(2+) may change by propagation of Ca(2+) changes through the nuclear envelope or by direct release of Ca(2+) inside the nucleus. In the last case nuclear and cytosolic signalling can be dissociated. Phosphatidylinositol bisphosphate, phospholipase C and cyclic ADP-ribosyl cyclase are present inside the nucleus. Inositol trisphosphate receptors (IP(3)R) and ryanodine receptors (RyR) have also been found in the nucleus and can be activated by agonists. Furthermore, nuclear location of the synthesizing enzymes and receptors may be atypical, not associated to the nuclear envelope or other membranes. The possible role of nuclear subdomains such as speckles, nucleoplasmic reticulum, multi-macromolecular complexes and nuclear nanovesicles is discussed.

摘要

钙离子信号对于控制基因转录很重要。细胞质钙离子([Ca2+](C))的变化可能促进转录因子或转录调节剂向核内迁移。核质钙离子([Ca2+](N))的变化也可以直接调节基因表达。[Ca2+](N)的变化可以通过核膜内的[Ca2+](C)变化的传播或通过核内的 Ca2+直接释放来实现。在后一种情况下,核和细胞质信号可以分离。双磷酸肌醇、磷脂酶 C 和环 ADP-核糖环化酶存在于核内。在核内还发现了三磷酸肌醇受体(IP3R)和兰尼碱受体(RyR),它们可以被激动剂激活。此外,合成酶和受体的核定位可能是非典型的,不与核膜或其他膜相关。讨论了核亚区如斑点、核质网、多分子复合物和核纳米囊泡的可能作用。

相似文献

1
Nuclear Ca(2+) signalling.核内钙离子信号转导。
Cell Calcium. 2011 May;49(5):280-9. doi: 10.1016/j.ceca.2010.11.004. Epub 2010 Dec 10.
2
Calcium release from ryanodine receptors in the nucleoplasmic reticulum.钙从核内质网中的兰尼碱受体释放。
Cell Calcium. 2006 Jan;39(1):65-73. doi: 10.1016/j.ceca.2005.09.010. Epub 2005 Nov 9.
3
Nuclear inositol 1,4,5-trisphosphate receptors regulate local Ca2+ transients and modulate cAMP response element binding protein phosphorylation.核肌醇1,4,5-三磷酸受体调节局部Ca2+瞬变并调节环磷酸腺苷反应元件结合蛋白磷酸化。
J Cell Sci. 2005 Jul 15;118(Pt 14):3131-40. doi: 10.1242/jcs.02446.
4
Presence of a putative vesicular inositol 1,4,5-trisphosphate-sensitive nucleoplasmic Ca2+ store.存在一种假定的对肌醇 1,4,5 - 三磷酸敏感的核质钙库。
Biochemistry. 2006 Feb 7;45(5):1362-73. doi: 10.1021/bi051837f.
5
Nuclear Ca2+ regulates cardiomyocyte function.细胞核内的钙离子调节心肌细胞功能。
Cell Calcium. 2008 Aug;44(2):230-42. doi: 10.1016/j.ceca.2007.11.016. Epub 2008 Jan 16.
6
Activation of ryanodine receptors in the nuclear envelope alters the conformation of the nuclear pore complex.核膜中兰尼碱受体的激活会改变核孔复合体的构象。
Biophys Chem. 2004 Dec 1;112(1):1-7. doi: 10.1016/j.bpc.2004.06.010.
7
Nuclear calcium signaling by inositol trisphosphate in GH3 pituitary cells.生长激素瘤(GH3)垂体细胞中肌醇三磷酸介导的核钙信号传导
Cell Calcium. 2008 Feb;43(2):205-14. doi: 10.1016/j.ceca.2007.05.005. Epub 2007 Jun 20.
8
Calcium microdomains in mitochondria and nucleus.线粒体和细胞核中的钙微区室
Cell Calcium. 2006 Nov-Dec;40(5-6):513-25. doi: 10.1016/j.ceca.2006.08.013. Epub 2006 Oct 25.
9
Amplification and propagation of pacemaker Ca2+ signals by cyclic ADP-ribose and the type 3 ryanodine receptor in T cells.环磷酸腺苷核糖和3型兰尼碱受体对T细胞中起搏钙信号的放大与传播
J Cell Sci. 2004 Apr 15;117(Pt 10):2141-9. doi: 10.1242/jcs.01063. Epub 2004 Mar 30.
10
Presence of a nucleoplasmic complex composed of the inositol 1,4,5-trisphosphate receptor/Ca2+ channel, chromogranin B, and phospholipids.存在一种由肌醇1,4,5-三磷酸受体/Ca2+通道、嗜铬粒蛋白B和磷脂组成的核质复合物。
Biochemistry. 2005 Jun 28;44(25):9246-54. doi: 10.1021/bi047427t.

引用本文的文献

1
Mechanisms for assembly of the nucleoplasmic reticulum.核质网组装的机制。
Cell Mol Life Sci. 2024 Oct 5;81(1):415. doi: 10.1007/s00018-024-05437-3.
2
Calcium modulates the tethering of BCOR-PRC1.1 enzymatic core to KDM2B via liquid-liquid phase separation.钙通过液-液相分离调节 BCOR-PRC1.1 酶核心与 KDM2B 的连接。
Commun Biol. 2024 Sep 10;7(1):1112. doi: 10.1038/s42003-024-06820-3.
3
T-type Ca2+ channels and their relationship with pre-neoplastic and neoplastic lesions in the human breast.T 型钙通道及其与人乳腺前瘤和瘤性病变的关系。
Braz J Med Biol Res. 2023 Feb 10;56:e11879. doi: 10.1590/1414-431X2023e11879. eCollection 2023.
4
The bitter end: T2R bitter receptor agonists elevate nuclear calcium and induce apoptosis in non-ciliated airway epithelial cells.苦不堪言:T2R 苦味受体激动剂可提高气道非纤毛上皮细胞核内钙离子浓度并诱导其凋亡。
Cell Calcium. 2022 Jan;101:102499. doi: 10.1016/j.ceca.2021.102499. Epub 2021 Nov 8.
5
IP Receptor Biology and Endoplasmic Reticulum Calcium Dynamics in Cancer.IP 受体生物学与内质网钙离子动力学在癌症中的作用
Prog Mol Subcell Biol. 2021;59:215-237. doi: 10.1007/978-3-030-67696-4_11.
6
The nucleus acts as a ruler tailoring cell responses to spatial constraints.细胞核作为一个标尺,对细胞响应的空间约束进行调整。
Science. 2020 Oct 16;370(6514). doi: 10.1126/science.aba2894.
7
Ouabain-Induced Cell Death and Survival. Role of α1-Na,K-ATPase-Mediated Signaling and [Na]/[K]-Dependent Gene Expression.哇巴因诱导的细胞死亡与存活。α1-钠钾-ATP酶介导的信号传导及[钠]/[钾]依赖性基因表达的作用。
Front Physiol. 2020 Sep 4;11:1060. doi: 10.3389/fphys.2020.01060. eCollection 2020.
8
NR1 and NR3B Composed Intranuclear -methyl-d-aspartate Receptor Complexes in Human Melanoma Cells.NR1 和 NR3B 在人黑色素瘤细胞中组成核内 -甲基-d-天冬氨酸受体复合物。
Int J Mol Sci. 2018 Jun 30;19(7):1929. doi: 10.3390/ijms19071929.
9
Na⁺,K⁺-Dependent and -Independent Signaling Triggered by Cardiotonic Steroids: Facts and Artifacts.强心甾类化合物引发的钠钾依赖性和非依赖性信号传导:事实与假象
Molecules. 2017 Apr 14;22(4):635. doi: 10.3390/molecules22040635.
10
Calpain-dependent disruption of nucleo-cytoplasmic transport in ALS motor neurons.肌萎缩侧索硬化症运动神经元中钙蛋白酶依赖性核质转运破坏。
Sci Rep. 2017 Jan 3;7:39994. doi: 10.1038/srep39994.