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本文引用的文献

1
EphrinB1/EphB3b Coordinate Bidirectional Epithelial-Mesenchymal Interactions Controlling Liver Morphogenesis and Laterality.EphrinB1/EphB3b协调双向上皮-间充质相互作用,控制肝脏形态发生和左右不对称性。
Dev Cell. 2016 Nov 7;39(3):316-328. doi: 10.1016/j.devcel.2016.10.009.
2
Loss of a Candidate Biliary Atresia Susceptibility Gene, add3a, Causes Biliary Developmental Defects in Zebrafish.一个潜在的胆道闭锁易感基因add3a的缺失导致斑马鱼的胆管发育缺陷。
J Pediatr Gastroenterol Nutr. 2016 Nov;63(5):524-530. doi: 10.1097/MPG.0000000000001375.
3
Iterative use of nuclear receptor Nr5a2 regulates multiple stages of liver and pancreas development.核受体Nr5a2的迭代使用调节肝脏和胰腺发育的多个阶段。
Dev Biol. 2016 Oct 1;418(1):108-123. doi: 10.1016/j.ydbio.2016.07.019. Epub 2016 Jul 26.
4
Loss of mtch2 function impairs early development of liver, intestine and visceral adipocytes in zebrafish larvae.mtch2功能丧失会损害斑马鱼幼体肝脏、肠道和内脏脂肪细胞的早期发育。
FEBS Lett. 2016 Sep;590(17):2852-61. doi: 10.1002/1873-3468.12330. Epub 2016 Aug 9.
5
Yap reprograms glutamine metabolism to increase nucleotide biosynthesis and enable liver growth.Yes相关蛋白通过重编程谷氨酰胺代谢来增加核苷酸生物合成并促进肝脏生长。
Nat Cell Biol. 2016 Aug;18(8):886-896. doi: 10.1038/ncb3389. Epub 2016 Jul 18.
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Endoderm specification and liver development.内胚层特化与肝脏发育。
Methods Cell Biol. 2016;134:463-83. doi: 10.1016/bs.mcb.2016.03.042. Epub 2016 May 24.
7
Glutathione antioxidant pathway activity and reserve determine toxicity and specificity of the biliary toxin biliatresone in zebrafish.谷胱甘肽抗氧化途径的活性和储备决定了胆汁毒素胆三烯在斑马鱼中的毒性和特异性。
Hepatology. 2016 Sep;64(3):894-907. doi: 10.1002/hep.28603. Epub 2016 Jun 11.
8
The toxin biliatresone causes mouse extrahepatic cholangiocyte damage and fibrosis through decreased glutathione and SOX17.毒素双氢胆甾烯酮通过降低谷胱甘肽和SOX17水平导致小鼠肝外胆管细胞损伤和纤维化。
Hepatology. 2016 Sep;64(3):880-93. doi: 10.1002/hep.28599. Epub 2016 May 20.
9
Modulation of tissue repair by regeneration enhancer elements.再生增强元件对组织修复的调节作用。
Nature. 2016 Apr 14;532(7598):201-6. doi: 10.1038/nature17644. Epub 2016 Apr 6.
10
Four and a Half LIM Domains 1b (Fhl1b) Is Essential for Regulating the Liver versus Pancreas Fate Decision and for β-Cell Regeneration.四半LIM结构域蛋白1b(Fhl1b)对于调控肝脏与胰腺的命运决定以及β细胞再生至关重要。
PLoS Genet. 2016 Feb 4;12(2):e1005831. doi: 10.1371/journal.pgen.1005831. eCollection 2016 Feb.

再度焕新:从斑马鱼研究洞察肝脏发育、再生与疾病

Making It New Again: Insight Into Liver Development, Regeneration, and Disease From Zebrafish Research.

作者信息

Wang Shuang, Miller Sophie R, Ober Elke A, Sadler Kirsten C

机构信息

Icahn School of Medicine at Mount Sinai, New York, NY, United States.

Danish Stem Cell Center (DanStem), University of Copenhagen, Copenhagen N, Denmark.

出版信息

Curr Top Dev Biol. 2017;124:161-195. doi: 10.1016/bs.ctdb.2016.11.012. Epub 2017 Jan 17.

DOI:10.1016/bs.ctdb.2016.11.012
PMID:28335859
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6450094/
Abstract

The adult liver of most vertebrates is predominantly comprised of hepatocytes. However, these cells must work in concert with biliary, stellate, vascular, and immune cells to accomplish the vast array of hepatic functions required for physiological homeostasis. Our understanding of liver development was accelerated as zebrafish emerged as an ideal vertebrate system to study embryogenesis. Through work in zebrafish and other models, it is now clear that the cells in the liver develop in a coordinated fashion during embryogenesis through a complex yet incompletely understood set of molecular guidelines. Zebrafish research has uncovered many key players that govern the acquisition of hepatic potential, cell fate, and plasticity. Although rare, some hepatobiliary diseases-especially biliary atresia-are caused by developmental defects; we discuss how research using zebrafish to study liver development has informed our understanding of and approaches to liver disease. The liver can be injured in response to an array of stressors including viral, mechanical/surgical, toxin-induced, immune-mediated, or inborn defects in metabolism. The liver has thus evolved the capacity to efficiently repair and regenerate. We discuss the emerging field of using zebrafish to study liver regeneration and highlight recent advances where zebrafish genetics and imaging approaches have provided novel insights into how cell plasticity contributes to liver regeneration.

摘要

大多数脊椎动物的成体肝脏主要由肝细胞组成。然而,这些细胞必须与胆管细胞、星状细胞、血管细胞和免疫细胞协同工作,以完成生理稳态所需的大量肝脏功能。随着斑马鱼成为研究胚胎发育的理想脊椎动物系统,我们对肝脏发育的理解得到了加速。通过对斑马鱼和其他模型的研究,现在很清楚,肝脏中的细胞在胚胎发育过程中通过一套复杂但尚未完全理解的分子指导以协调的方式发育。斑马鱼研究发现了许多控制肝脏潜能获得、细胞命运和可塑性的关键因素。尽管罕见,但一些肝胆疾病——尤其是胆道闭锁——是由发育缺陷引起的;我们讨论了利用斑马鱼研究肝脏发育的研究如何增进了我们对肝脏疾病的理解和治疗方法。肝脏可能会因一系列应激源而受损,包括病毒、机械/手术、毒素诱导、免疫介导或先天性代谢缺陷。因此,肝脏进化出了高效修复和再生的能力。我们讨论了利用斑马鱼研究肝脏再生的新兴领域,并强调了斑马鱼遗传学和成像方法在细胞可塑性如何促进肝脏再生方面提供了新见解的最新进展。