• 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

对肌醇六磷酸激酶1(IP6K1)在哺乳动物细胞过程中作用的见解。

Insights into the roles of inositol hexakisphosphate kinase 1 (IP6K1) in mammalian cellular processes.

作者信息

Chakkour Mohamed, Greenberg Miriam L

机构信息

Department of Biological Sciences, Wayne State University, Detroit, Michigan, USA.

Department of Biological Sciences, Wayne State University, Detroit, Michigan, USA.

出版信息

J Biol Chem. 2024 Apr;300(4):107116. doi: 10.1016/j.jbc.2024.107116. Epub 2024 Feb 24.

DOI:10.1016/j.jbc.2024.107116
PMID:38403246
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11065760/
Abstract

Inositol phosphates and their metabolites play a significant role in several biochemical pathways, gene expression regulation, and phosphate homeostasis. Among the different inositol phosphates, inositol hexakisphosphate (IP6) is a substrate of inositol hexakisphosphate kinases (IP6Ks), which phosphorylate one or more of the IP6 phosphate groups. Pyrophosphorylation of IP6 leads to the formation of inositol pyrophosphates, high-energy signaling molecules that mediate physiological processes through their ability to modify target protein activities, either by directly binding to their target protein or by pyrophosphorylating protein serine residues. 5-diphosphoinositol pentakisphosphate, the most abundant inositol pyrophosphate in mammals, has been extensively studied and found to be significantly involved in a wide range of physiological processes. Three IP6K (IP6K1, IP6K2, and IP6K3) isoforms regulate IP7 synthesis in mammals. Here, we summarize our current understanding of IP6K1's roles in cytoskeletal remodeling, trafficking, cellular migration, metabolism, gene expression, DNA repair, and immunity. We also briefly discuss current gaps in knowledge, highlighting the need for further investigation.

摘要

肌醇磷酸及其代谢产物在多种生化途径、基因表达调控和磷酸盐稳态中发挥着重要作用。在不同的肌醇磷酸中,肌醇六磷酸(IP6)是肌醇六磷酸激酶(IP6Ks)的底物,该激酶可使IP6的一个或多个磷酸基团磷酸化。IP6的焦磷酸化导致肌醇焦磷酸的形成,肌醇焦磷酸是一种高能信号分子,通过直接结合靶蛋白或使蛋白丝氨酸残基焦磷酸化来修饰靶蛋白活性,从而介导生理过程。5-二磷酸肌醇五磷酸是哺乳动物中最丰富的肌醇焦磷酸,已被广泛研究,并发现其显著参与多种生理过程。三种IP6K(IP6K1、IP6K2和IP6K3)同工型调节哺乳动物中IP7的合成。在此,我们总结了目前对IP6K1在细胞骨架重塑、运输、细胞迁移、代谢、基因表达、DNA修复和免疫中的作用的理解。我们还简要讨论了当前知识上的空白,强调了进一步研究的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/150e/11065760/2e38f834a249/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/150e/11065760/83b54176c140/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/150e/11065760/b6495e3a73df/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/150e/11065760/cf389b59c7dd/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/150e/11065760/2e38f834a249/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/150e/11065760/83b54176c140/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/150e/11065760/b6495e3a73df/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/150e/11065760/cf389b59c7dd/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/150e/11065760/2e38f834a249/gr4.jpg

相似文献

1
Insights into the roles of inositol hexakisphosphate kinase 1 (IP6K1) in mammalian cellular processes.对肌醇六磷酸激酶1(IP6K1)在哺乳动物细胞过程中作用的见解。
J Biol Chem. 2024 Apr;300(4):107116. doi: 10.1016/j.jbc.2024.107116. Epub 2024 Feb 24.
2
Deletion of inositol hexakisphosphate kinase 1 (IP6K1) reduces cell migration and invasion, conferring protection from aerodigestive tract carcinoma in mice.肌醇六磷酸激酶1(IP6K1)的缺失会降低细胞迁移和侵袭能力,为小鼠的气消化道癌提供保护。
Cell Signal. 2016 Aug;28(8):1124-36. doi: 10.1016/j.cellsig.2016.04.011. Epub 2016 Apr 30.
3
Inositol Pyrophosphates: Signaling Molecules with Pleiotropic Actions in Mammals.肌醇六磷酸酯:哺乳动物中具有多种作用的信号分子。
Molecules. 2020 May 8;25(9):2208. doi: 10.3390/molecules25092208.
4
Inositol Pyrophosphates as Versatile Metabolic Messengers.肌醇焦磷酸作为多功能代谢信使。
Annu Rev Biochem. 2024 Aug;93(1):317-338. doi: 10.1146/annurev-biochem-030222-121901.
5
Inositol hexakisphosphate kinase 1 (IP6K1) activity is required for cytoplasmic dynein-driven transport.肌醇六磷酸激酶1(IP6K1)的活性是胞质动力蛋白驱动运输所必需的。
Biochem J. 2016 Oct 1;473(19):3031-47. doi: 10.1042/BCJ20160610. Epub 2016 Jul 29.
6
The inositol hexakisphosphate kinases IP6K1 and -2 regulate human cellular phosphate homeostasis, including XPR1-mediated phosphate export.肌醇六磷酸激酶 IP6K1 和 -2 调节人体细胞内的磷酸盐稳态,包括 XPR1 介导体外磷酸盐输出。
J Biol Chem. 2019 Jul 26;294(30):11597-11608. doi: 10.1074/jbc.RA119.007848. Epub 2019 Jun 11.
7
Inositol hexakisphosphate kinase-2 determines cellular energy dynamics by regulating creatine kinase-B.肌醇六磷酸激酶-2通过调节肌酸激酶-B 来决定细胞能量动态。
Proc Natl Acad Sci U S A. 2021 Feb 9;118(6). doi: 10.1073/pnas.2020695118.
8
Inositol Hexakisphosphate Kinase-3 Regulates the Morphology and Synapse Formation of Cerebellar Purkinje Cells via Spectrin/Adducin.肌醇六磷酸激酶-3通过血影蛋白/内收蛋白调节小脑浦肯野细胞的形态和突触形成。
J Neurosci. 2015 Aug 5;35(31):11056-67. doi: 10.1523/JNEUROSCI.1069-15.2015.
9
Inositol Hexakisphosphate Kinase-2 in Cerebellar Granule Cells Regulates Purkinje Cells and Motor Coordination via Protein 4.1N.小脑颗粒细胞中的肌醇六磷酸激酶-2 通过蛋白 4.1N 调节浦肯野细胞和运动协调。
J Neurosci. 2018 Aug 22;38(34):7409-7419. doi: 10.1523/JNEUROSCI.1165-18.2018. Epub 2018 Jul 13.
10
Inositol pyrophosphate profiling reveals regulatory roles of IP6K2-dependent enhanced IP metabolism in the enteric nervous system.肌醇六磷酸激酶 2 依赖性增强的肌醇六磷酸代谢在肠神经系统中的调控作用的焦磷酸肌醇谱分析。
J Biol Chem. 2023 Mar;299(3):102928. doi: 10.1016/j.jbc.2023.102928. Epub 2023 Jan 19.

引用本文的文献

1
Regulatory Effects of Endometriosis-Associated Genetic Variants: A Multi-Tissue eQTL Analysis.子宫内膜异位症相关基因变异的调控作用:多组织表达数量性状基因座分析
Diseases. 2025 Aug 6;13(8):248. doi: 10.3390/diseases13080248.
2
Valproate independently activates Snf1, inhibits TORC1, and induces repression of INO1 transcription by increasing nuclear localization of Opi1.丙戊酸盐可独立激活Snf1,抑制TORC1,并通过增加Opi1的核定位来诱导INO1转录的抑制。
Sci Rep. 2025 Jul 9;15(1):24601. doi: 10.1038/s41598-025-07540-2.
3
Inositols and Bone Health: Potential Therapeutic Applications in Osteoporosis Prevention and Treatment.

本文引用的文献

1
Interaction with IP6K1 supports pyrophosphorylation of substrate proteins by the inositol pyrophosphate 5-InsP7.与 IP6K1 的相互作用支持由肌醇六磷酸 5-InsP7 对底物蛋白进行焦磷酸化。
Biosci Rep. 2024 Oct 30;44(10). doi: 10.1042/BSR20240792.
2
Depleting inositol pyrophosphate 5-InsP7 protected the heart against ischaemia-reperfusion injury by elevating plasma adiponectin.耗竭肌醇五磷酸 5-InsP7 通过提高血浆脂联素水平保护心脏免受缺血再灌注损伤。
Cardiovasc Res. 2024 Jul 2;120(8):954-970. doi: 10.1093/cvr/cvae017.
3
Inositol hexakisphosphate kinase 1 is essential for cell junction integrity in the mouse seminiferous epithelium.
肌醇与骨骼健康:在骨质疏松症预防和治疗中的潜在治疗应用
Nutrients. 2025 Jun 13;17(12):1999. doi: 10.3390/nu17121999.
4
Inositol Phosphates and Synthesizing Enzymes: Implications in Neurodegenerative Disorders.肌醇磷酸酯与合成酶:对神经退行性疾病的影响
Biomolecules. 2025 Feb 4;15(2):225. doi: 10.3390/biom15020225.
5
Towards Improved Bioavailability of Cereal Inositol Phosphates, -Inositol and Phenolic Acids.提高谷物肌醇磷酸酯、肌醇和酚酸的生物利用度
Molecules. 2025 Feb 1;30(3):652. doi: 10.3390/molecules30030652.
6
On the Possible Effect of Phytic Acid (Myo-Inositol Hexaphosphoric Acid, IP6) on Cytochromes P450 and Systems of Xenobiotic Metabolism in Different Hepatic Models.植酸(肌醇六磷酸,IP6)对不同肝模型细胞色素 P450 及外源物质代谢系统的可能影响。
Int J Mol Sci. 2024 Mar 23;25(7):3610. doi: 10.3390/ijms25073610.
肌醇六磷酸激酶 1 对于精子表皮细胞连接完整性至关重要。
Biochim Biophys Acta Mol Cell Res. 2024 Jan;1871(1):119596. doi: 10.1016/j.bbamcr.2023.119596. Epub 2023 Sep 22.
4
Itraconazole inhibits endothelial cell migration by disrupting inositol pyrophosphate-dependent focal adhesion dynamics and cytoskeletal remodeling.伊曲康唑通过破坏肌醇五磷酸依赖的焦点黏附动力学和细胞骨架重构来抑制内皮细胞迁移。
Biomed Pharmacother. 2023 May;161:114449. doi: 10.1016/j.biopha.2023.114449. Epub 2023 Feb 27.
5
Pharmacological Inhibition of Inositol Hexakisphosphate Kinase 1 Protects Mice against Obesity-Induced Bone Loss.肌醇六磷酸激酶1的药理学抑制可保护小鼠免受肥胖诱导的骨质流失。
Biology (Basel). 2022 Aug 24;11(9):1257. doi: 10.3390/biology11091257.
6
Phosphatidic acid inhibits inositol synthesis by inducing nuclear translocation of kinase IP6K1 and repression of myo-inositol-3-P synthase.磷酸脂抑制肌醇合成由诱导激酶 IP6K1 的核易位和肌醇-3-P 合酶的抑制所引起。
J Biol Chem. 2022 Sep;298(9):102363. doi: 10.1016/j.jbc.2022.102363. Epub 2022 Aug 10.
7
Inositol hexakisphosphate kinases differentially regulate trafficking of vesicular glutamate transporters 1 and 2.肌醇六磷酸激酶差异性调节囊泡型谷氨酸转运体1和2的转运。
Front Cell Neurosci. 2022 Jul 22;16:926794. doi: 10.3389/fncel.2022.926794. eCollection 2022.
8
New Insights Into the Biology of Protein O-GlcNAcylation: Approaches and Observations.蛋白质O-连接N-乙酰葡糖胺糖基化生物学的新见解:方法与观察
Front Aging. 2021 Mar 12;1:620382. doi: 10.3389/fragi.2020.620382. eCollection 2020.
9
Deletion of IP6K1 in mice accelerates tumor growth by dysregulating the tumor-immune microenvironment.在小鼠中删除IP6K1会通过失调肿瘤免疫微环境来加速肿瘤生长。
Anim Cells Syst (Seoul). 2022 Jan 31;26(1):19-27. doi: 10.1080/19768354.2022.2029560. eCollection 2022.
10
Whole Body Deletion Protects Mice from Age-Induced Weight Gain, Insulin Resistance and Metabolic Dysfunction.全身缺失可保护小鼠免受年龄诱导的体重增加、胰岛素抵抗和代谢功能障碍。
Int J Mol Sci. 2022 Feb 12;23(4):2059. doi: 10.3390/ijms23042059.