Key Laboratory of Freshwater Fish Reproduction and Development, Ministry of Education, Laboratory of Molecular Developmental Biology, School of Life Sciences, Southwest University, Beibei, Chongqing, China.
Key Laboratory of Freshwater Fish Reproduction and Development, Ministry of Education, Laboratory of Molecular Developmental Biology, School of Life Sciences, Southwest University, Beibei, Chongqing, China.
Gastroenterology. 2014 Mar;146(3):789-800.e8. doi: 10.1053/j.gastro.2013.11.045. Epub 2013 Dec 4.
BACKGROUND & AIMS: The liver has high regenerative capacity, but it is not clear whether most biliary cells (particularly larger cholangiocytes) transdifferentiate into hepatocytes in regenerating liver. We investigated how this process might contribute to liver regeneration in zebrafish.
Zebrafish transgenic lines were generated using the standard I-SceI meganuclease transgenesis technique. Hepatocytes of the Tg(lfabp:mCherry-NTR)(cq2) animals were ablated by the administration of metronidazole. We investigated transdifferentiation of biliary cells to hepatocytes and expression of markers using whole mount antibody staining, fluorescent in situ hybridization, and Cre/loxP-based genetic lineage tracing analyses. The role of biliary cells in hepatocyte regeneration was explored using zebrafish larvae with defects in biliary cell development.
After extreme loss of hepatocytes, nearly all the biliary cells steadily lost their tubular morphology, proliferated, and expressed hepatocyte-specific markers. Cre/loxP-based inducible lineage tracing showed that new hepatocytes mainly arose from transdifferentiation of biliary cells; this process required Notch signaling and, in turn, activation of Sox9b in cholangiocytes. Activation of early endoderm and hepatoblast markers in most of the cholangiocytes indicated that biliary transdifferentiation includes a step of dedifferentiation into a bipotential intermediate. Defects in development of biliary cells impaired hepatocyte regeneration.
Using our zebrafish liver regeneration model, we found that biliary cells can transdifferentiate into hepatocytes and are the major contributors to hepatocyte regeneration after extreme hepatocyte loss.
肝脏具有很强的再生能力,但目前尚不清楚大多数胆管细胞(尤其是较大的胆管细胞)是否在再生的肝脏中转分化为肝细胞。我们研究了这一过程如何促进斑马鱼的肝脏再生。
使用标准的 I-SceI 核酸酶转基因组技术生成了斑马鱼转基因系。通过甲硝唑给药来消融 Tg(lfabp:mCherry-NTR)(cq2)动物的肝细胞。我们通过全胚胎抗体染色、荧光原位杂交和 Cre/loxP 基于遗传谱系追踪分析来研究胆管细胞向肝细胞的转分化和标志物的表达。使用胆管细胞发育缺陷的斑马鱼幼虫来探索胆管细胞在肝细胞再生中的作用。
在极端丧失肝细胞后,几乎所有的胆管细胞都稳定地失去了管状形态,增殖并表达了肝细胞特异性标志物。Cre/loxP 诱导的谱系追踪显示,新的肝细胞主要来源于胆管细胞的转分化;这个过程需要 Notch 信号通路,进而激活胆管细胞中的 Sox9b。大多数胆管细胞中早期内胚层和肝母细胞标志物的激活表明胆管转分化包括去分化为双潜能中间阶段的步骤。胆管细胞发育缺陷会损害肝细胞再生。
使用我们的斑马鱼肝脏再生模型,我们发现胆管细胞可以转分化为肝细胞,并且是在极端肝细胞丧失后肝细胞再生的主要贡献者。