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Human umbilical cord mesenchymal stem cells enhance liver regeneration and decrease collagen content in fibrosis mice after partial hepatectomy by activating Wnt/β-catenin signaling.人脐带间充质干细胞通过激活Wnt/β-连环蛋白信号通路增强肝再生并降低部分肝切除术后纤维化小鼠的胶原含量。
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Vitamin D Receptor Regulates Liver Regeneration After Partial Hepatectomy in Male Mice.维生素 D 受体调控雄性小鼠肝部分切除术后的肝脏再生。
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The killifish germline regulates longevity and somatic repair in a sex-specific manner.食蚊鱼生殖系以性别特异性方式调控寿命和体组织修复。
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Single-center experience in 127 adult patients, mono or dual artificial liver support therapy, in patients with acute liver failure.对127例成年急性肝衰竭患者进行单中心单或双人肝支持治疗的经验。
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本文引用的文献

1
Small RNAs are on the move.小 RNA 正在移动。
Nature. 2010 Sep 23;467(7314):415-9. doi: 10.1038/nature09351.
2
Loss of c-Met disrupts gene expression program required for G2/M progression during liver regeneration in mice.c-Met 缺失会破坏小鼠肝再生过程中 G2/M 进展所需的基因表达程序。
PLoS One. 2010 Sep 16;5(9):e12739. doi: 10.1371/journal.pone.0012739.
3
The ploidy conveyor of mature hepatocytes as a source of genetic variation.成熟肝细胞的倍性 conveyor 作为遗传变异的来源。
Nature. 2010 Oct 7;467(7316):707-10. doi: 10.1038/nature09414. Epub 2010 Sep 22.
4
Suppression of liver regeneration and hepatocyte proliferation in hepatocyte-targeted glypican 3 transgenic mice.肝靶向聚糖蛋白 3 转基因小鼠中肝再生和肝细胞增殖的抑制。
Hepatology. 2010 Sep;52(3):1060-7. doi: 10.1002/hep.23794.
5
Induced pluripotent stem cell-derived hepatocytes have the functional and proliferative capabilities needed for liver regeneration in mice.诱导多能干细胞衍生的肝细胞具有在小鼠中进行肝脏再生所需的功能和增殖能力。
J Clin Invest. 2010 Sep;120(9):3120-6. doi: 10.1172/JCI43267. Epub 2010 Aug 25.
6
Paracrine signals from mesenchymal cell populations govern the expansion and differentiation of human hepatic stem cells to adult liver fates.间质细胞群体分泌的旁分泌信号调控人类肝干细胞向成体肝脏命运的扩增和分化。
Hepatology. 2010 Oct;52(4):1443-54. doi: 10.1002/hep.23829.
7
Epithelial-to-mesenchymal transition in liver fibrosis: dead or alive?肝纤维化中的上皮-间质转化:是死是活?
Gastroenterology. 2010 Sep;139(3):722-5. doi: 10.1053/j.gastro.2010.07.015. Epub 2010 Aug 1.
8
Nf2/Merlin controls progenitor homeostasis and tumorigenesis in the liver.NF2/Merlin 控制肝脏祖细胞的自我平衡和肿瘤发生。
Genes Dev. 2010 Aug 15;24(16):1718-30. doi: 10.1101/gad.1938710. Epub 2010 Jul 30.
9
Genetic labeling does not detect epithelial-to-mesenchymal transition of cholangiocytes in liver fibrosis in mice.遗传标记不能检测到小鼠肝纤维化中胆管细胞的上皮间质转化。
Gastroenterology. 2010 Sep;139(3):987-98. doi: 10.1053/j.gastro.2010.05.005. Epub 2010 Jun 20.
10
Recent advances in liver stem cell therapy.肝脏干细胞治疗的最新进展。
Curr Opin Gastroenterol. 2010 Jul;26(4):395-402. doi: 10.1097/MOG.0b013e32833a6bec.

肝脏再生的新概念。

New concepts in liver regeneration.

机构信息

Department of Surgery, University of Washington, Seattle, USA.

出版信息

J Gastroenterol Hepatol. 2011 Jan;26 Suppl 1(Suppl 1):203-12. doi: 10.1111/j.1440-1746.2010.06539.x.

DOI:10.1111/j.1440-1746.2010.06539.x
PMID:21199532
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3077908/
Abstract

The unique ability of the liver to regenerate itself has fascinated biologists for years and has made it the prototype for mammalian organ regeneration. Harnessing this process has great potential benefit in the treatment of liver failure and has been the focus of intense research over the past 50 years. Not only will detailed understanding of cell proliferation in response to injury be applicable to other dysfunction of organs, it may also shed light on how cancer develops in a cirrhotic liver, in which there is intense pressure on cells to regenerate. Advances in molecular techniques over the past few decades have led to the identification of many regulatory intermediates, and pushed us onto the verge of an explosive era in regenerative medicine. To date, more than 10 clinical trials have been reported in which augmented regeneration using progenitor cell therapy has been attempted in human patients. This review traces the path that has been taken over the last few decades in the study of liver regeneration, highlights new concepts in the field, and discusses the challenges that still stand between us and clinical therapy.

摘要

肝脏自身具有的再生能力多年来一直令生物学家着迷,使其成为哺乳动物器官再生的原型。利用这一过程在治疗肝衰竭方面具有巨大的潜在益处,在过去 50 年中一直是研究的重点。不仅对损伤后细胞增殖的详细了解将适用于其他器官功能障碍,还可能揭示在肝硬化中癌症是如何发展的,因为在肝硬化中,细胞面临着强烈的再生压力。过去几十年中分子技术的进步已经导致了许多调节中间体的鉴定,并将我们推向了再生医学的爆炸时代的边缘。迄今为止,已经报道了 10 多项临床试验,其中尝试了使用祖细胞疗法增强人类患者的再生。本综述追溯了过去几十年中在肝脏再生研究中所走过的道路,强调了该领域的新概念,并讨论了我们在临床治疗之间仍然存在的挑战。