• 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

肝胆汁酸摄取转运体和 HBV 进入受体 NTCP 的分子调控。

Molecular regulation of the hepatic bile acid uptake transporter and HBV entry receptor NTCP.

机构信息

Tytgat Institute for Liver and Intestinal Research, Amsterdam University Medical Centers Amsterdam, the Netherlands; Amsterdam Gastroenterology, Endocrinology, Metabolism (AGEM), Amsterdam, the Netherlands.

Institute of Virology, Technische Universität München/Helmholtz Zentrum München, Munich, Germany.

出版信息

Biochim Biophys Acta Mol Cell Biol Lipids. 2021 Aug;1866(8):158960. doi: 10.1016/j.bbalip.2021.158960. Epub 2021 Apr 29.

DOI:10.1016/j.bbalip.2021.158960
PMID:33932583
Abstract

Transporters expressed by hepatocytes and enterocytes play a critical role in maintaining the enterohepatic circulation of bile acids. The sodium taurocholate cotransporting polypeptide (NTCP), exclusively expressed at the basolateral side of hepatocytes, mediates the uptake of conjugated bile acids. In conditions where bile flow is impaired (cholestasis), pharmacological inhibition of NTCP-mediated bile acid influx is suggested to reduce hepatocellular damage due to bile acid overload. Furthermore, NTCP has been shown to play an important role in hepatitis B virus (HBV) and hepatitis Delta virus (HDV) infection by functioning as receptor for viral entry into hepatocytes. This review provides a summary of current molecular insight into the regulation of NTCP expression at the plasma membrane, hepatic bile acid transport, and NTCP-mediated viral infection.

摘要

肝细胞和肠细胞表达的转运蛋白在维持胆汁酸的肠肝循环中起着关键作用。牛磺胆酸钠共转运多肽(NTCP),仅在肝细胞的基底外侧表达,介导结合胆汁酸的摄取。在胆汁流动受损(胆汁淤积)的情况下,建议抑制 NTCP 介导的胆汁酸内流的药理学方法,以减少由于胆汁酸过载导致的肝细胞损伤。此外,NTCP 已被证明在乙型肝炎病毒(HBV)和丁型肝炎病毒(HDV)感染中发挥重要作用,作为病毒进入肝细胞的受体。本综述总结了目前对 NTCP 在质膜表达、肝内胆汁酸转运和 NTCP 介导的病毒感染中的调节的分子认识。

相似文献

1
Molecular regulation of the hepatic bile acid uptake transporter and HBV entry receptor NTCP.肝胆汁酸摄取转运体和 HBV 进入受体 NTCP 的分子调控。
Biochim Biophys Acta Mol Cell Biol Lipids. 2021 Aug;1866(8):158960. doi: 10.1016/j.bbalip.2021.158960. Epub 2021 Apr 29.
2
Viral entry of hepatitis B and D viruses and bile salts transportation share common molecular determinants on sodium taurocholate cotransporting polypeptide.乙型肝炎和丁型肝炎病毒的病毒进入以及胆汁盐转运共用牛磺胆酸钠共转运多肽上的共同分子决定因素。
J Virol. 2014 Mar;88(6):3273-84. doi: 10.1128/JVI.03478-13. Epub 2014 Jan 3.
3
Reduced hepatitis B and D viral entry using clinically applied drugs as novel inhibitors of the bile acid transporter NTCP.利用临床应用药物作为新型胆酸转运蛋白 NTCP 抑制剂,减少乙型肝炎和丁型肝炎病毒进入。
Sci Rep. 2017 Nov 10;7(1):15307. doi: 10.1038/s41598-017-15338-0.
4
Kinetics of the bile acid transporter and hepatitis B virus receptor Na+/taurocholate cotransporting polypeptide (NTCP) in hepatocytes.肝细胞中胆汁酸转运蛋白和乙型肝炎病毒受体钠离子/牛磺胆酸钠共转运多肽(NTCP)的动力学。
J Hepatol. 2014 Oct;61(4):867-75. doi: 10.1016/j.jhep.2014.05.018. Epub 2014 May 15.
5
Sodium taurocholate cotransporting polypeptide is a functional receptor for human hepatitis B and D virus.牛磺胆酸钠共转运多肽是乙型肝炎病毒和丁型肝炎病毒的功能性受体。
Elife. 2012 Nov 13;1:e00049. doi: 10.7554/eLife.00049.
6
Hepatitis B and D viruses exploit sodium taurocholate co-transporting polypeptide for species-specific entry into hepatocytes.乙型肝炎和丁型肝炎病毒利用牛磺胆酸钠共转运多肽进行种属特异性进入肝细胞。
Gastroenterology. 2014 Apr;146(4):1070-83. doi: 10.1053/j.gastro.2013.12.024. Epub 2013 Dec 19.
7
Cyclosporin derivatives inhibit hepatitis B virus entry without interfering with NTCP transporter activity.环孢素衍生物可抑制乙型肝炎病毒进入,而不干扰钠-牛磺胆酸共转运多肽(NTCP)转运体活性。
J Hepatol. 2017 Apr;66(4):685-692. doi: 10.1016/j.jhep.2016.11.009. Epub 2016 Nov 25.
8
Long-term -inhibition of the hepatitis B and D virus receptor NTCP by taurolithocholic acid.牛磺胆酸对乙型肝炎和丁型肝炎病毒受体 NTCP 的长期抑制作用。
Am J Physiol Gastrointest Liver Physiol. 2021 Jan 1;320(1):G66-G80. doi: 10.1152/ajpgi.00263.2020. Epub 2020 Nov 11.
9
Impaired uptake of conjugated bile acids and hepatitis b virus pres1-binding in na(+) -taurocholate cotransporting polypeptide knockout mice.在钠离子-牛磺胆酸盐共转运多肽基因敲除小鼠中,结合型胆汁酸摄取受损及乙肝病毒前S1结合受损。
Hepatology. 2015 Jul;62(1):207-19. doi: 10.1002/hep.27694. Epub 2015 May 8.
10
Primary biliary acids inhibit hepatitis D virus (HDV) entry into human hepatoma cells expressing the sodium-taurocholate cotransporting polypeptide (NTCP).初级胆汁酸抑制丁型肝炎病毒(HDV)进入表达牛磺胆酸钠共转运多肽(NTCP)的人肝癌细胞。
PLoS One. 2015 Feb 3;10(2):e0117152. doi: 10.1371/journal.pone.0117152. eCollection 2015.

引用本文的文献

1
Updates on Recent Advancements in Hepatitis D Virus Treatment.丁型肝炎病毒治疗的最新进展
Viruses. 2025 Aug 10;17(8):1100. doi: 10.3390/v17081100.
2
Liver-specific Nr1h4 deletion in mice with human-like bile acid composition causes severe liver injury.在具有类人胆汁酸组成的小鼠中肝脏特异性Nr1h4缺失会导致严重肝损伤。
J Lipid Res. 2025 Jul;66(7):100839. doi: 10.1016/j.jlr.2025.100839. Epub 2025 Jun 9.
3
Identification of NTCP animal orthologs supporting hepatitis B virus binding and infection.支持乙型肝炎病毒结合与感染的NTCP动物直系同源物的鉴定。
J Virol. 2025 Apr 15;99(4):e0183324. doi: 10.1128/jvi.01833-24. Epub 2025 Mar 5.
4
Drug-induced cholestasis (DIC) predictions based on in vitro inhibition of major bile acid clearance mechanisms.基于体外对主要胆汁酸清除机制的抑制作用对药物性胆汁淤积(DIC)进行预测。
Arch Toxicol. 2025 Jan;99(1):377-391. doi: 10.1007/s00204-024-03895-z. Epub 2024 Nov 14.
5
The Culprit Behind HBV-Infected Hepatocytes: NTCP.HBV 感染肝细胞的罪魁祸首:NTCP。
Drug Des Devel Ther. 2024 Oct 28;18:4839-4858. doi: 10.2147/DDDT.S480151. eCollection 2024.
6
Oleanolic acid improved intestinal immune function by activating and potentiating bile acids receptor signaling in E. coli-challenged piglets.齐墩果酸通过激活和增强大肠杆菌攻击的仔猪胆汁酸受体信号通路来改善肠道免疫功能。
J Anim Sci Biotechnol. 2024 May 18;15(1):79. doi: 10.1186/s40104-024-01037-0.
7
Evolutionary analysis of SLC10 family members and insights into function and expression regulation of lamprey NTCP.SLC10家族成员的进化分析及对七鳃鳗NTCP功能与表达调控的见解
Fish Physiol Biochem. 2024 Jun;50(3):1109-1122. doi: 10.1007/s10695-024-01324-7. Epub 2024 Mar 2.
8
Alterations in zonal distribution and plasma membrane localization of hepatocyte bile acid transporters in patients with NAFLD.非酒精性脂肪性肝病患者肝细胞胆汁酸转运体的区域分布和质膜定位改变。
Hepatol Commun. 2024 Feb 14;8(3). doi: 10.1097/HC9.0000000000000377. eCollection 2024 Mar 1.
9
Structural basis of hepatitis B virus receptor binding.乙型肝炎病毒受体结合的结构基础。
Nat Struct Mol Biol. 2024 Mar;31(3):447-454. doi: 10.1038/s41594-023-01191-5. Epub 2024 Jan 17.
10
Bile acids, gut microbiota, and therapeutic insights in hepatocellular carcinoma.胆汁酸、肠道微生物群与肝细胞癌的治疗新视角。
Cancer Biol Med. 2023 Dec 23;21(2):144-62. doi: 10.20892/j.issn.2095-3941.2023.0394.