• 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

胆管细胞对损伤反应的机制。

Mechanisms of cholangiocyte responses to injury.

机构信息

Department of Medicine, Texas A&M Health Science Center, College of Medicine, Temple, TX, United States.

Research, Central Texas Veterans Health Care System, Temple, TX, United States; Scott & White Digestive Disease Research Center, Baylor Scott & White Health, Temple, TX, United States; Academic Research Integration, Baylor Scott & White Health, Temple, TX, United States; Department of Medicine, Texas A&M Health Science Center, College of Medicine, Temple, TX, United States.

出版信息

Biochim Biophys Acta Mol Basis Dis. 2018 Apr;1864(4 Pt B):1262-1269. doi: 10.1016/j.bbadis.2017.06.017. Epub 2017 Jun 23.

DOI:10.1016/j.bbadis.2017.06.017
PMID:28648950
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5742086/
Abstract

Cholangiocytes, epithelial cells that line the biliary epithelium, are the primary target cells for cholangiopathies including primary sclerosing cholangitis and primary biliary cholangitis. Quiescent cholangiocytes respond to biliary damage and acquire an activated neuroendocrine phenotype to maintain the homeostasis of the liver. The typical response of cholangiocytes is proliferation leading to bile duct hyperplasia, which is a characteristic of cholestatic liver diseases. Current studies have identified various signaling pathways that are associated with cholangiocyte proliferation/loss and liver fibrosis in cholangiopathies using human samples and rodent models. Although recent studies have demonstrated that extracellular vesicles and microRNAs could be mediators that regulate these messenger/receptor axes, further studies are required to confirm their roles. This review summarizes current studies of biliary response and cholangiocyte proliferation during cholestatic liver injury with particular emphasis on the secretin/secretin receptor axis. This article is part of a Special Issue entitled: Cholangiocytes in Health and Diseaseedited by Jesus Banales, Marco Marzioni, Nicholas LaRusso and Peter Jansen.

摘要

胆管细胞是排列在胆管上皮的上皮细胞,是包括原发性硬化性胆管炎和原发性胆汁性胆管炎在内的胆管疾病的主要靶细胞。静止的胆管细胞对胆管损伤作出反应,并获得激活的神经内分泌表型,以维持肝脏的内稳态。胆管细胞的典型反应是增殖导致胆管增生,这是胆汁淤积性肝病的特征。目前的研究已经使用人类样本和啮齿动物模型确定了与胆管疾病中胆管细胞增殖/丢失和肝纤维化相关的各种信号通路。尽管最近的研究表明,细胞外囊泡和 microRNAs 可能是调节这些信使/受体轴的介质,但仍需要进一步的研究来确认它们的作用。这篇综述总结了目前关于胆汁淤积性肝损伤期间胆管反应和胆管细胞增殖的研究,特别强调了分泌素/分泌素受体轴。本文是由 Jesus Banales、Marco Marzioni、Nicholas LaRusso 和 Peter Jansen 编辑的特刊“健康和疾病中的胆管细胞”的一部分。

相似文献

1
Mechanisms of cholangiocyte responses to injury.胆管细胞对损伤反应的机制。
Biochim Biophys Acta Mol Basis Dis. 2018 Apr;1864(4 Pt B):1262-1269. doi: 10.1016/j.bbadis.2017.06.017. Epub 2017 Jun 23.
2
Bile acid receptors in the biliary tree: TGR5 in physiology and disease.胆管树中的胆汁酸受体:TGR5 在生理和疾病中的作用。
Biochim Biophys Acta Mol Basis Dis. 2018 Apr;1864(4 Pt B):1319-1325. doi: 10.1016/j.bbadis.2017.08.021. Epub 2017 Aug 25.
3
Pathophysiologic implications of innate immunity and autoinflammation in the biliary epithelium.先天免疫和胆管上皮细胞自身炎症在病理生理学中的意义。
Biochim Biophys Acta Mol Basis Dis. 2018 Apr;1864(4 Pt B):1374-1379. doi: 10.1016/j.bbadis.2017.07.023. Epub 2017 Jul 25.
4
MicroRNAs and extracellular vesicles in cholangiopathies.微小 RNA 与细胞外囊泡在胆管疾病中的作用。
Biochim Biophys Acta Mol Basis Dis. 2018 Apr;1864(4 Pt B):1293-1307. doi: 10.1016/j.bbadis.2017.06.026. Epub 2017 Jul 13.
5
Cholangiocytes in the pathogenesis of primary sclerosing cholangitis and development of cholangiocarcinoma.原发性硬化性胆管炎发病机制和胆管癌发生中的胆管细胞。
Biochim Biophys Acta Mol Basis Dis. 2018 Apr;1864(4 Pt B):1390-1400. doi: 10.1016/j.bbadis.2017.08.020. Epub 2017 Aug 25.
6
Drug-induced bile duct injury.药物性胆管损伤。
Biochim Biophys Acta Mol Basis Dis. 2018 Apr;1864(4 Pt B):1498-1506. doi: 10.1016/j.bbadis.2017.08.033. Epub 2017 Sep 4.
7
Role of inflammation and proinflammatory cytokines in cholangiocyte pathophysiology.炎症和促炎细胞因子在胆管细胞病理生理学中的作用。
Biochim Biophys Acta Mol Basis Dis. 2018 Apr;1864(4 Pt B):1270-1278. doi: 10.1016/j.bbadis.2017.07.024. Epub 2017 Jul 25.
8
Animal models of biliary injury and altered bile acid metabolism.动物模型的胆汁淤积损伤和胆汁酸代谢改变。
Biochim Biophys Acta Mol Basis Dis. 2018 Apr;1864(4 Pt B):1254-1261. doi: 10.1016/j.bbadis.2017.06.027. Epub 2017 Jul 11.
9
The role of the secretin/secretin receptor axis in inflammatory cholangiocyte communication via extracellular vesicles.分泌素/分泌素受体轴在细胞外囊泡介导的炎症性胆管细胞通讯中的作用。
Sci Rep. 2017 Sep 11;7(1):11183. doi: 10.1038/s41598-017-10694-3.
10
Pathobiology of biliary epithelia.胆道上皮的病理生物学。
Biochim Biophys Acta Mol Basis Dis. 2018 Apr;1864(4 Pt B):1220-1231. doi: 10.1016/j.bbadis.2017.06.024. Epub 2017 Jul 15.

引用本文的文献

1
Liver Regeneration as a Model for Studying Cellular Plasticity in Mammals: The Roles of Hepatocytes and Cholangiocytes.肝脏再生作为研究哺乳动物细胞可塑性的模型:肝细胞和胆管细胞的作用。
Cells. 2025 Jul 22;14(15):1129. doi: 10.3390/cells14151129.
2
Gradual DNA methylation changes reveal transcription factors implicated in metabolic dysfunction-associated steatotic liver disease progression and epigenetic age acceleration.逐渐发生的DNA甲基化变化揭示了与代谢功能障碍相关的脂肪性肝病进展和表观遗传年龄加速有关的转录因子。
Clin Epigenetics. 2025 Aug 4;17(1):138. doi: 10.1186/s13148-025-01945-6.
3
The pivotal role of dysregulated autophagy in the progression of non-alcoholic fatty liver disease.

本文引用的文献

1
Knockdown of Hepatic Gonadotropin-Releasing Hormone by Vivo-Morpholino Decreases Liver Fibrosis in Multidrug Resistance Gene 2 Knockout Mice by Down-Regulation of miR-200b.通过体内吗啉代寡核苷酸敲低肝脏促性腺激素释放激素可通过下调miR-200b减轻多药耐药基因2敲除小鼠的肝纤维化。
Am J Pathol. 2017 Jul;187(7):1551-1565. doi: 10.1016/j.ajpath.2017.03.013. Epub 2017 May 12.
2
Substance P increases liver fibrosis by differential changes in senescence of cholangiocytes and hepatic stellate cells.P物质通过胆管细胞和肝星状细胞衰老的差异变化增加肝纤维化。
Hepatology. 2017 Aug;66(2):528-541. doi: 10.1002/hep.29138. Epub 2017 Jun 19.
3
自噬失调在非酒精性脂肪性肝病进展中的关键作用。
Front Endocrinol (Lausanne). 2024 Aug 8;15:1374644. doi: 10.3389/fendo.2024.1374644. eCollection 2024.
4
Overcoming treatment resistance in cholangiocarcinoma: current strategies, challenges, and prospects.克服胆管癌的治疗耐药性:当前策略、挑战与前景
Front Cell Dev Biol. 2024 Aug 2;12:1408852. doi: 10.3389/fcell.2024.1408852. eCollection 2024.
5
Cholangiocyte organoids to study drug-induced injury.胆管细胞类器官用于研究药物诱导损伤。
Stem Cell Res Ther. 2024 Mar 13;15(1):78. doi: 10.1186/s13287-024-03692-6.
6
Cellular heterogeneity and plasticity during NAFLD progression.非酒精性脂肪性肝病进展过程中的细胞异质性和可塑性。
Front Mol Biosci. 2023 Aug 11;10:1221669. doi: 10.3389/fmolb.2023.1221669. eCollection 2023.
7
Clonorchis sinensis granulin promotes malignant transformation of human intrahepatic biliary epithelial cells through interaction with M2 macrophages via regulation of STAT3  phosphorylation and the MEK/ERK pathway.华支睾吸虫颗粒蛋白通过与 M2 巨噬细胞相互作用,通过调节 STAT3 磷酸化和 MEK/ERK 通路促进人肝内胆管上皮细胞的恶性转化。
Parasit Vectors. 2023 Apr 24;16(1):139. doi: 10.1186/s13071-023-05765-6.
8
Bile Acids and Biliary Fibrosis.胆汁酸与胆汁性纤维化。
Cells. 2023 Mar 2;12(5):792. doi: 10.3390/cells12050792.
9
Survey of infection in imported Romani and local sheep (), and potential epidemiological role in Saudi Arabia.沙特阿拉伯进口罗姆羊和本地羊的感染情况调查及其潜在的流行病学作用。
J Anim Sci Technol. 2022 Nov;64(6):1215-1225. doi: 10.5187/jast.2022.e63. Epub 2022 Nov 30.
10
Metabolomics- and systems toxicology-based hepatotoxicity mechanism of in rats.基于代谢组学和系统毒理学的大鼠肝毒性机制
Front Pharmacol. 2022 Nov 18;13:1015008. doi: 10.3389/fphar.2022.1015008. eCollection 2022.
The Neuropeptide Galanin Is Up-Regulated during Cholestasis and Contributes to Cholangiocyte Proliferation.
神经肽甘丙肽在胆汁淤积期间上调并促进胆管细胞增殖。
Am J Pathol. 2017 Apr;187(4):819-830. doi: 10.1016/j.ajpath.2016.12.015. Epub 2017 Feb 11.
4
The role of sphingosine 1-phosphate receptor 2 in bile-acid-induced cholangiocyte proliferation and cholestasis-induced liver injury in mice.1-磷酸鞘氨醇受体2在胆汁酸诱导的小鼠胆管细胞增殖及胆汁淤积性肝损伤中的作用
Hepatology. 2017 Jun;65(6):2005-2018. doi: 10.1002/hep.29076. Epub 2017 Apr 28.
5
Bile duct ligation-induced biliary hyperplasia, hepatic injury, and fibrosis are reduced in mast cell-deficient Kit mice.在肥大细胞缺陷的Kit小鼠中,胆管结扎诱导的胆管增生、肝损伤和纤维化有所减轻。
Hepatology. 2017 Jun;65(6):1991-2004. doi: 10.1002/hep.29079. Epub 2017 Apr 28.
6
Primary Sclerosing Cholangitis.原发性硬化性胆管炎
N Engl J Med. 2016 Sep 22;375(12):1161-70. doi: 10.1056/NEJMra1506330.
7
Extracellular vesicles in liver pathobiology: Small particles with big impact.肝脏病理生物学中的细胞外囊泡:影响重大的小颗粒。
Hepatology. 2016 Dec;64(6):2219-2233. doi: 10.1002/hep.28814. Epub 2016 Oct 20.
8
The roles of bile acids and sphingosine-1-phosphate signaling in the hepatobiliary diseases.胆汁酸和鞘氨醇-1-磷酸信号在肝胆疾病中的作用。
J Lipid Res. 2016 Sep;57(9):1636-43. doi: 10.1194/jlr.R069286. Epub 2016 Jul 26.
9
Pathogenesis of Kupffer Cells in Cholestatic Liver Injury.库普弗细胞在胆汁淤积性肝损伤中的发病机制。
Am J Pathol. 2016 Sep;186(9):2238-47. doi: 10.1016/j.ajpath.2016.06.003. Epub 2016 Jul 22.
10
Regulators of Cholangiocyte Proliferation.胆管细胞增殖的调节因子
Gene Expr. 2017 Feb 10;17(2):155-171. doi: 10.3727/105221616X692568. Epub 2016 Jul 12.