• 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

相似文献

1
Lipid microdomains and the regulation of ion channel function.脂质微区与离子通道功能的调节。
J Physiol. 2010 Sep 1;588(Pt 17):3169-78. doi: 10.1113/jphysiol.2010.191585. Epub 2010 Jun 2.
2
Targeting of ion channels to membrane microdomains: localization of KV channels to lipid rafts.离子通道在膜微区的靶向定位:钾离子通道在脂筏中的定位
Trends Pharmacol Sci. 2004 Jan;25(1):16-21. doi: 10.1016/j.tips.2003.11.007.
3
Lipid microdomains and k(+) channel compartmentation: detergent and non-detergent-based methods for the isolation and characterisation of cholesterol-enriched lipid rafts.脂质微区与钾离子通道区室化:基于去污剂和非去污剂的方法用于分离和表征富含胆固醇的脂筏。
Methods Mol Biol. 2008;491:91-101. doi: 10.1007/978-1-59745-526-8_7.
4
Ceramide selectively displaces cholesterol from ordered lipid domains (rafts): implications for lipid raft structure and function.神经酰胺可选择性地将胆固醇从有序脂质结构域(脂筏)中置换出来:对脂筏结构与功能的影响。
J Biol Chem. 2004 Mar 12;279(11):9997-10004. doi: 10.1074/jbc.M309992200. Epub 2003 Dec 29.
5
Functional role of lipid raft microdomains in cyclic nucleotide-gated channel activation.脂筏微区在环核苷酸门控通道激活中的功能作用。
Mol Pharmacol. 2004 Mar;65(3):503-11. doi: 10.1124/mol.65.3.503.
6
Lipids as targeting signals: lipid rafts and intracellular trafficking.脂质作为靶向信号:脂筏与细胞内运输
Traffic. 2004 Apr;5(4):247-54. doi: 10.1111/j.1600-0854.2004.0181.x.
7
[Cholesterol and lipid rafts in the biological membranes. Role in the release, reception and ion channel functions].[生物膜中的胆固醇与脂筏。在释放、接收及离子通道功能中的作用]
Usp Fiziol Nauk. 2013 Jan-Mar;44(1):17-38.
8
Localization of ion channels to lipid Raft domains within the cardiovascular system.离子通道在心血管系统内脂质筏结构域中的定位。
Trends Cardiovasc Med. 2004 Feb;14(2):37-42. doi: 10.1016/j.tcm.2003.10.002.
9
Effects of membrane lipids on ion channel structure and function.膜脂对离子通道结构与功能的影响。
Cell Biochem Biophys. 2003;38(2):161-90. doi: 10.1385/CBB:38:2:161.
10
Lipid rafts/caveolae as microdomains of calcium signaling.脂筏/小窝作为钙信号的微区
Cell Calcium. 2009 Jun;45(6):625-33. doi: 10.1016/j.ceca.2009.02.009. Epub 2009 Mar 25.

引用本文的文献

1
Peripheral gene dysregulation in Negr1-deficient mice: insights into possible links with affective behavior.Negr1基因缺陷小鼠的外周基因失调:对与情感行为可能联系的见解。
Front Mol Neurosci. 2025 Jul 8;18:1602201. doi: 10.3389/fnmol.2025.1602201. eCollection 2025.
2
Biochemical Modification and Subcellular Trafficking of Urea Transporters.尿素转运蛋白的生化修饰与亚细胞转运
Subcell Biochem. 2025;118:63-85. doi: 10.1007/978-981-96-6898-4_4.
3
Relationship between elevated serum direct bilirubin and atrial fibrillation risk among patients with coronary artery disease.冠心病患者血清直接胆红素升高与心房颤动风险之间的关系。
Front Med (Lausanne). 2025 Feb 14;12:1405682. doi: 10.3389/fmed.2025.1405682. eCollection 2025.
4
Targeting the hERG1/β1 integrin complex in lipid rafts potentiates statins anti-cancer activity in pancreatic cancer.靶向脂筏中的hERG1/β1整合素复合物可增强他汀类药物在胰腺癌中的抗癌活性。
Cell Death Discov. 2025 Feb 3;11(1):39. doi: 10.1038/s41420-025-02321-2.
5
Effect of the Membrane Environment on Pharmacologic Inhibition of hERG K Channel Activity.膜环境对人乙醚-a- go-go相关基因(hERG)钾通道活性的药理学抑制作用
JACC Clin Electrophysiol. 2025 Apr;11(4):708-719. doi: 10.1016/j.jacep.2024.11.016. Epub 2025 Jan 29.
6
Unveiling Interactions between Self-Assembling Peptides and Neuronal Membranes.揭示自组装肽与神经元膜之间的相互作用。
Langmuir. 2024 Dec 24;40(51):26811-26823. doi: 10.1021/acs.langmuir.4c02050. Epub 2024 Dec 9.
7
L-shaped association of plasma low-density lipoprotein cholesterol with atrial fibrillation recurrence after catheter ablation: a prospective cohort study.血浆低密度脂蛋白胆固醇 L 型与导管消融后心房颤动复发的相关性:一项前瞻性队列研究。
Sci Rep. 2024 Nov 18;14(1):28434. doi: 10.1038/s41598-024-79836-8.
8
Membrane lipid nanodomains modulate HCN pacemaker channels in nociceptor DRG neurons.膜脂纳米域调节伤害感受器 DRG 神经元中的 HCN 起搏通道。
Nat Commun. 2024 Nov 15;15(1):9898. doi: 10.1038/s41467-024-54053-z.
9
Apolipoprotein-L1 (APOL1): From Sleeping Sickness to Kidney Disease.载脂蛋白 L1(APOL1):从昏睡病到肾病。
Cells. 2024 Oct 20;13(20):1738. doi: 10.3390/cells13201738.
10
Electrocontractile remodeling of isolated cardiomyocytes induced during early-stage hypercholesterolemia.早期高胆固醇血症诱导的分离心肌细胞的电收缩重塑。
J Bioenerg Biomembr. 2024 Aug;56(4):373-387. doi: 10.1007/s10863-024-10026-x. Epub 2024 Jun 13.

本文引用的文献

1
α1-adrenoceptors regulate only the caveolae-located subpopulation of cardiac K(V)4 channels.α1-肾上腺素受体仅调节心脏 K(V)4 通道位于 caveolae 的亚群。
Channels (Austin). 2010 May-Jun;4(3):168-78. doi: 10.4161/chan.4.3.11479.
2
Disruption of the maxi-K-caveolin-1 interaction alters current expression in human myometrial cells.破坏巨电导钙激活钾通道-1 与 caveolin-1 的相互作用改变了人子宫平滑肌细胞的电流表达。
Reprod Biol Endocrinol. 2009 Nov 23;7:131. doi: 10.1186/1477-7827-7-131.
3
Activation of TRPC1 by STIM1 in ER-PM microdomains involves release of the channel from its scaffold caveolin-1.内质网-质膜微域中 STIM1 对 TRPC1 的激活涉及通道从其支架蛋白 caveolin-1 上释放。
Proc Natl Acad Sci U S A. 2009 Nov 24;106(47):20087-92. doi: 10.1073/pnas.0905002106. Epub 2009 Nov 6.
4
Sphingolipid/cholesterol regulation of neurotransmitter receptor conformation and function.鞘脂/胆固醇对神经递质受体构象和功能的调节
Biochim Biophys Acta. 2009 Nov;1788(11):2345-61. doi: 10.1016/j.bbamem.2009.08.016. Epub 2009 Sep 3.
5
Caveolin-3 negatively regulates recombinant cardiac K(ATP) channels.小窝蛋白-3对重组心肌ATP敏感性钾通道起负性调节作用。
Biochem Biophys Res Commun. 2009 Jul 31;385(3):472-7. doi: 10.1016/j.bbrc.2009.05.100. Epub 2009 May 27.
6
A distinct pool of phosphatidylinositol 4,5-bisphosphate in caveolae revealed by a nanoscale labeling technique.一种纳米级标记技术揭示的小窝中独特的磷脂酰肌醇4,5-二磷酸池。
Proc Natl Acad Sci U S A. 2009 Jun 9;106(23):9256-61. doi: 10.1073/pnas.0900216106. Epub 2009 May 22.
7
Identification of a C-terminus domain critical for the sensitivity of Kir2.1 to cholesterol.鉴定对Kir2.1对胆固醇敏感性至关重要的C末端结构域。
Proc Natl Acad Sci U S A. 2009 May 12;106(19):8055-60. doi: 10.1073/pnas.0809847106. Epub 2009 Apr 29.
8
Caveolae, ion channels and cardiac arrhythmias.小窝、离子通道与心律失常
Prog Biophys Mol Biol. 2008 Oct-Nov;98(2-3):149-60. doi: 10.1016/j.pbiomolbio.2009.01.012. Epub 2009 Jan 30.
9
The activity of the epithelial sodium channels is regulated by caveolin-1 via a Nedd4-2-dependent mechanism.上皮钠通道的活性通过一种Nedd4-2依赖机制由小窝蛋白-1调节。
J Biol Chem. 2009 May 8;284(19):12663-9. doi: 10.1074/jbc.M809737200. Epub 2009 Mar 20.
10
Caveolin-3 associates with and affects the function of hyperpolarization-activated cyclic nucleotide-gated channel 4.小窝蛋白-3与超极化激活的环核苷酸门控通道4相互作用并影响其功能。
Biochemistry. 2008 Nov 25;47(47):12312-8.

脂质微区与离子通道功能的调节。

Lipid microdomains and the regulation of ion channel function.

机构信息

Biosciences Building, School of Biological Sciences, University of Liverpool, Crown Street, Liverpool L69 7ZB, UK.

出版信息

J Physiol. 2010 Sep 1;588(Pt 17):3169-78. doi: 10.1113/jphysiol.2010.191585. Epub 2010 Jun 2.

DOI:10.1113/jphysiol.2010.191585
PMID:20519314
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2976012/
Abstract

Many types of ion channel localize to cholesterol and sphingolipid-enriched regions of the plasma membrane known as lipid microdomains or 'rafts'. The precise physiological role of these unique lipid microenvironments remains elusive due largely to difficulties associated with studying these potentially extremely small and dynamic domains. Nevertheless, increasing evidence suggests that membrane rafts regulate channel function in a number of different ways. Raft-enriched lipids such as cholesterol and sphingolipids exert effects on channel activity either through direct protein-lipid interactions or by influencing the physical properties of the bilayer. Rafts also appear to selectively recruit interacting signalling molecules to generate subcellular compartments that may be important for efficient and selective signal transduction. Direct interaction with raft-associated scaffold proteins such as caveolin can also influence channel function by altering gating kinetics or by affecting trafficking and surface expression. Selective association of ion channels with specific lipid microenvironments within the membrane is thus likely to be an important and fundamental regulatory aspect of channel physiology. This brief review highlights some of the existing evidence for raft modulation of channel function.

摘要

许多类型的离子通道定位于质膜中富含胆固醇和鞘脂的区域,这些区域被称为脂质微区或“筏”。由于研究这些潜在的极小且动态的域存在困难,这些独特的脂质微环境的确切生理作用仍然难以捉摸。然而,越来越多的证据表明,膜筏以多种不同的方式调节通道功能。富含筏的脂质,如胆固醇和鞘脂,通过直接的蛋白-脂质相互作用或通过影响双层的物理性质,对通道活性产生影响。筏似乎还选择性地招募相互作用的信号分子,以产生可能对有效和选择性信号转导很重要的亚细胞隔室。与窖蛋白等筏相关支架蛋白的直接相互作用也可以通过改变门控动力学或影响运输和表面表达来影响通道功能。因此,离子通道与膜内特定脂质微环境的选择性结合可能是通道生理学的一个重要和基本的调节方面。这篇简短的综述强调了一些关于筏调节通道功能的现有证据。