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本文引用的文献

1
TGR5 in cholangiocytes.TGR5 在胆管细胞中。
Curr Opin Gastroenterol. 2013 May;29(3):299-304. doi: 10.1097/MOG.0b013e32835f3f14.
2
PDX-1/Hes-1 interactions determine cholangiocyte proliferative response to injury in rodents: possible implications for sclerosing cholangitis.PDX-1/Hes-1 相互作用决定了啮齿动物胆管细胞对损伤的增殖反应:对硬化性胆管炎的可能影响。
J Hepatol. 2013 Apr;58(4):750-6. doi: 10.1016/j.jhep.2012.11.033. Epub 2012 Nov 30.
3
Analysis of altered microRNA expression profiles in peripheral blood mononuclear cells from patients with primary biliary cirrhosis.原发性胆汁性肝硬化患者外周血单个核细胞中差异表达 microRNA 的分析。
J Gastroenterol Hepatol. 2013 Mar;28(3):543-50. doi: 10.1111/jgh.12040.
4
Modulation of the biliary expression of arylalkylamine N-acetyltransferase alters the autocrine proliferative responses of cholangiocytes in rats.调节胆管道上皮细胞芳香族胺 N-乙酰基转移酶的表达可改变大鼠胆管细胞的自分泌增殖反应。
Hepatology. 2013 Mar;57(3):1130-41. doi: 10.1002/hep.26105. Epub 2013 Feb 7.
5
Yes-associated protein regulates the hepatic response after bile duct ligation.Yes 相关蛋白调控胆管结扎后的肝脏应答。
Hepatology. 2012 Sep;56(3):1097-107. doi: 10.1002/hep.25769. Epub 2012 Aug 8.
6
Multipotent stem/progenitor cells in the human foetal biliary tree.人胎胆管中的多能干细胞/祖细胞。
J Hepatol. 2012 Nov;57(5):987-94. doi: 10.1016/j.jhep.2012.07.013. Epub 2012 Jul 20.
7
Insignificant effect of secretin in rodent models of polycystic kidney and liver disease.在多囊肾病和肝病的啮齿动物模型中,生长抑素的作用不显著。
Am J Physiol Renal Physiol. 2012 Oct;303(7):F1089-98. doi: 10.1152/ajprenal.00242.2012. Epub 2012 Jul 18.
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Hepatic progenitor cells activation, fibrosis, and adipokines production in pediatric nonalcoholic fatty liver disease.肝祖细胞激活、纤维化和肝内脂肪细胞因子在儿童非酒精性脂肪性肝病中的产生。
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Macrophage-derived Wnt opposes Notch signaling to specify hepatic progenitor cell fate in chronic liver disease.巨噬细胞衍生的 Wnt 信号拮抗 Notch 信号以在慢性肝病中特异性地决定肝祖细胞命运。
Nat Med. 2012 Mar 4;18(4):572-9. doi: 10.1038/nm.2667.
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Up-regulation of microRNA 506 leads to decreased Cl-/HCO3- anion exchanger 2 expression in biliary epithelium of patients with primary biliary cirrhosis.微小 RNA506 的上调导致原发性胆汁性肝硬化患者胆管上皮中 Cl-/HCO3-阴离子交换器 2 的表达减少。
Hepatology. 2012 Aug;56(2):687-97. doi: 10.1002/hep.25691. Epub 2012 Jul 10.

胆管上皮形态和功能异质性的最新进展。

Recent advances in the morphological and functional heterogeneity of the biliary epithelium.

机构信息

Department of Medicine, Division Gastroenterology, Texas A&M Health Science Center, College of Medicine, TX, USA.

出版信息

Exp Biol Med (Maywood). 2013 May;238(5):549-65. doi: 10.1177/1535370213489926.

DOI:10.1177/1535370213489926
PMID:23856906
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3965268/
Abstract

This review focuses on the recent advances related to the heterogeneity of different-sized bile ducts with regard to the morphological and phenotypical characteristics, and the differential secretory, apoptotic and proliferative responses of small and large cholangiocytes to gastrointestinal hormones/peptides, neuropeptides and toxins. We describe several in vivo and in vitro models used for evaluating biliary heterogeneity. Subsequently, we discuss the heterogeneous proliferative and apoptotic responses of small and large cholangiocytes to liver injury and the mechanisms regulating the differentiation of small into large (more differentiated) cholangiocytes. Following a discussion on the heterogeneity of stem/progenitor cells in the biliary epithelium, we outline the heterogeneity of bile ducts in human cholangiopathies. After a summary section, we discuss the future perspectives that will further advance the field of the functional heterogeneity of the biliary epithelium.

摘要

这篇综述重点介绍了不同大小胆管在形态和表型特征方面的异质性,以及小和大胆管细胞对胃肠激素/肽、神经肽和毒素的分泌、凋亡和增殖反应的差异。我们描述了几种用于评估胆管异质性的体内和体外模型。随后,我们讨论了小和大胆管细胞对肝损伤的增殖和凋亡反应的异质性,以及调节小胆管细胞分化为大(更分化)胆管细胞的机制。在讨论了胆管上皮中的干细胞/祖细胞的异质性之后,我们概述了人类胆管疾病中胆管的异质性。在总结部分,我们讨论了未来的展望,这将进一步推动胆管上皮功能异质性领域的发展。