Li F B, Zhao H, Peng K R, Gao Z G, Huang S J, Tou J F, Shu X L, Gu W Z
Department of Gastroenterology, Children's Hospital of Zhejiang University, Hangzhou, China.
Department of General Surgery, Children's Hospital of Zhejiang University, Hangzhou, China.
Genet Mol Res. 2016 Feb 19;15(1):gmr7217. doi: 10.4238/gmr.15017217.
We investigated the expression of transforming growth factor-β1 (TGF-β1) and connective tissue growth factor (CTGF) in the liver tissue of infants with congenital biliary atresia and neonatal hepatitis, as well as the relationship between the expression of the two factors and liver fibrosis. Thirty-six infants who met the cholestasis criteria were classified into congenital biliary atresia and neonatal hepatitis groups. All specimens were stained with hematoxylin and eosin and Masson's trichrome, and the degree of liver fibrosis was assessed. The scope and level of CTGF and TGF-β1 expression in the different specimens was evaluated by immunohistochemistry and observation. Liver fibrosis in the congenital biliary atresia group was more advanced than that in the neonatal hepatitis group, and the difference was significant (P < 0.01). In the neonatal hepatitis patients, CTGF and TGF-β1 were mainly expressed in the hepatocytes, while they were expressed in both hepatocytes and biliary epithelial cells in the congenital biliary atresia patients, and in these patients the expression was significantly stronger than in the neonatal hepatitis patients (P < 0.01). With the aggravation of hepatic fibrosis, CTGF and TGF-β1 expression levels in liver tissue gradually increased, and their expression levels were significantly correlated (P < 0.01). Liver fibrosis is present in both congenital biliary atresia and neonatal hepatitis patients. The gradual increase of CTGF and TGF-β1 expression levels in liver tissue is associated with liver fibrosis. Early expression of CTGF and TGF-β1 in biliary epithelial cells may be involved in the pathogenesis of congenital biliary atresia.
我们研究了先天性胆道闭锁和新生儿肝炎患儿肝组织中转化生长因子-β1(TGF-β1)和结缔组织生长因子(CTGF)的表达情况,以及这两种因子的表达与肝纤维化之间的关系。36例符合胆汁淤积标准的婴儿被分为先天性胆道闭锁组和新生儿肝炎组。所有标本均进行苏木精-伊红染色和Masson三色染色,并评估肝纤维化程度。通过免疫组织化学和观察评估不同标本中CTGF和TGF-β1表达的范围和水平。先天性胆道闭锁组的肝纤维化程度比新生儿肝炎组更严重,差异有统计学意义(P<0.01)。在新生儿肝炎患者中,CTGF和TGF-β1主要在肝细胞中表达,而在先天性胆道闭锁患者中,它们在肝细胞和胆管上皮细胞中均有表达,且这些患者中的表达明显强于新生儿肝炎患者(P<0.01)。随着肝纤维化的加重,肝组织中CTGF和TGF-β1的表达水平逐渐升高,且它们的表达水平显著相关(P<0.01)。先天性胆道闭锁和新生儿肝炎患者均存在肝纤维化。肝组织中CTGF和TGF-β1表达水平的逐渐升高与肝纤维化有关。胆管上皮细胞中CTGF和TGF-β1的早期表达可能参与先天性胆道闭锁的发病机制。