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刺猬索尼克在发育与修复中的奇遇。II. 刺猬索尼克与肝脏发育、炎症及癌症

The adventures of sonic hedgehog in development and repair. II. Sonic hedgehog and liver development, inflammation, and cancer.

作者信息

Omenetti Alessia, Diehl Anna Mae

机构信息

Duke University Medical Center, Division of Gastroenterology, Department of Medicine, Durham, NC 27710, USA.

出版信息

Am J Physiol Gastrointest Liver Physiol. 2008 Mar;294(3):G595-8. doi: 10.1152/ajpgi.00543.2007. Epub 2008 Jan 24.

Abstract

Hedgehog (Hh) signaling modulates tissue remodeling by controlling the fate of Hh-responsive cells. Healthy adult livers exhibit little Hh activity. However, cells involved in adult liver repair, including myofibroblasts and progenitors, are capable of producing and responding to Hh ligands. During adult liver injury, Hh ligand production increases and populations of Hh-responsive cells expand. This process is accompanied by fibrosis. Ligand production and Hh-responsive cells diminish as fibrosis resolves and normal hepatic architecture is restored, but Hh signaling persists in hepatocellular carcinomas. These findings suggest that the Hh pathway mediates remodeling responses that are triggered by adult liver damage.

摘要

刺猬信号通路(Hh)通过控制Hh反应性细胞的命运来调节组织重塑。健康的成年肝脏几乎没有Hh活性。然而,参与成年肝脏修复的细胞,包括肌成纤维细胞和祖细胞,能够产生并对Hh配体作出反应。在成年肝脏损伤期间,Hh配体的产生增加,Hh反应性细胞群体扩大。这个过程伴随着纤维化。随着纤维化的消退和正常肝结构的恢复,配体产生和Hh反应性细胞减少,但Hh信号通路在肝细胞癌中持续存在。这些发现表明,Hh通路介导了由成年肝脏损伤引发的重塑反应。

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