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Hepatocyte-specific Ablation in Zebrafish to Study Biliary-driven Liver Regeneration
Authors:Tae-Young Choi  Mehwish Khaliq  Sungjin Ko  Juhoon So  Donghun Shin
Affiliation:1.Department of Developmental Biology, McGowan Institute for Regenerative Medicine, University of Pittsburgh
Abstract:The liver has a great capacity to regenerate. Hepatocytes, the parenchymal cells of the liver, can regenerate in one of two ways: hepatocyte- or biliary-driven liver regeneration. In hepatocyte-driven liver regeneration, regenerating hepatocytes are derived from preexisting hepatocytes, whereas, in biliary-driven regeneration, regenerating hepatocytes are derived from biliary epithelial cells (BECs). For hepatocyte-driven liver regeneration, there are excellent rodent models that have significantly contributed to the current understanding of liver regeneration. However, no such rodent model exists for biliary-driven liver regeneration. We recently reported on a zebrafish liver injury model in which BECs extensively give rise to hepatocytes upon severe hepatocyte loss. In this model, hepatocytes are specifically ablated by a pharmacogenetic means. Here we present in detail the methods to ablate hepatocytes and to analyze the BEC-driven liver regeneration process. This hepatocyte-specific ablation model can be further used to discover the underlying molecular and cellular mechanisms of biliary-driven liver regeneration. Moreover, these methods can be applied to chemical screens to identify small molecules that augment or suppress liver regeneration.
Keywords:Developmental Biology   Issue 99   nitroreductase   metronidazole   biliary epithelial cells   hepatocytes   zebrafish   liver regeneration   cell ablation   transgenic
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