Department of Medicine, University of California, San Diego, La Jolla, California, USA.
Gastroenterology. 2010 Sep;139(3):987-98. doi: 10.1053/j.gastro.2010.05.005. Epub 2010 Jun 20.
BACKGROUND & AIMS: Chronic injury changes the fate of certain cellular populations, inducing epithelial cells to generate fibroblasts by epithelial-to-mesenchymal transition (EMT) and mesenchymal cells to generate epithelial cells by mesenchymal-to-epithelial transition (MET). Although contribution of EMT/MET to embryogenesis, renal fibrosis, and lung fibrosis is well documented, role of EMT/MET in liver fibrosis is unclear. We determined whether cytokeratin-19 positive (K19(+)) cholangiocytes give rise to myofibroblasts (EMT) and/or whether glial fibrillary acidic protein positive (GFAP(+)) hepatic stellate cells (HSCs) can express epithelial markers (MET) in response to experimental liver injury.
EMT was studied with Cre-loxP system to map cell fate of K19(+) cholangiocytes in K19(YFP) or fibroblast-specific protein-1 (FSP-1)(YFP) mice, generated by crossing tamoxifen-inducible K19(CreERT) mice or FSP-1(Cre) mice with Rosa26(f/f-YFP) mice. MET of GFAP(+) HSCs was studied in GFAP(GFP) mice. Mice were subjected to bile duct ligation or CCl(4)-liver injury, and livers were analyzed for expression of mesodermal and epithelial markers.
On Cre-loxP recombination, >40% of genetically labeled K19(+) cholangiocytes expressed yellow fluorescent protein (YFP). All mice developed liver fibrosis. However, specific immunostaining of K19(YFP) cholangiocytes showed no expression of EMT markers alpha-smooth muscle actin, desmin, or FSP-1. Moreover, cells genetically labeled by FSP-1(YFP) expression did not coexpress cholangiocyte markers K19 or E-cadherin. Genetically labeled GFAP(GFP) HSCs did not express epithelial or liver progenitor markers in response to liver injury.
EMT of cholangiocytes identified by genetic labeling does not contribute to hepatic fibrosis in mice. Likewise, GFAP(Cre)-labeled HSCs showed no coexpression of epithelial markers, providing no evidence for MET in HSCs in response to fibrogenic liver injury.
慢性损伤改变了某些细胞群体的命运,通过上皮-间充质转化(EMT)使上皮细胞产生成纤维细胞,通过间充质-上皮转化(MET)使间充质细胞产生上皮细胞。虽然 EMT/MET 对胚胎发生、肾纤维化和肺纤维化的作用已有充分的文献记载,但 EMT/MET 在肝纤维化中的作用尚不清楚。我们确定了 CK19 阳性(K19(+))胆管细胞是否产生肌成纤维细胞(EMT),以及胶质纤维酸性蛋白阳性(GFAP(+))肝星状细胞(HSCs)是否可以在实验性肝损伤时表达上皮标记物(MET)。
通过 Cre-loxP 系统研究 EMT,以描绘 K19(YFP)或纤维蛋白特异性蛋白 1 (FSP-1)(YFP)小鼠中 K19(+)胆管细胞的细胞命运,这些小鼠是通过将他莫昔芬诱导型 K19(CreERT)小鼠或 FSP-1(Cre)小鼠与 Rosa26(f/f-YFP)小鼠杂交而产生的。在 GFAP(GFP)小鼠中研究了 GFAP(+)HSCs 的 MET。对小鼠进行胆管结扎或 CCl4-肝损伤,分析肝脏中中胚层和上皮标记物的表达。
在 Cre-loxP 重组后,>40%的遗传标记 K19(+)胆管细胞表达黄色荧光蛋白(YFP)。所有小鼠均发生肝纤维化。然而,K19(YFP)胆管细胞的特异性免疫染色未显示 EMT 标记物α-平滑肌肌动蛋白、结蛋白或 FSP-1 的表达。此外,通过 FSP-1(YFP)表达遗传标记的细胞也不共表达胆管细胞标记物 K19 或 E-钙粘蛋白。对肝损伤无反应时,遗传标记的 GFAP(GFP)HSCs 不表达上皮或肝祖细胞标记物。
通过遗传标记鉴定的胆管细胞 EMT 不会导致小鼠肝纤维化。同样,GFAP(Cre)标记的 HSCs 也没有表达上皮标记物,这为 HSCs 在应对纤维生成性肝损伤时没有 MET 提供了证据。