论文部分内容阅读
rn目的探讨IL-33在肺纤维化模型小鼠的表达。方法小鼠气管内一次性注入博来霉素制备急性肺纤维化模型(BLM组,20只),气管内注入等容积生理盐水作为对照(对照组,20只)。HE染色观察肺部炎症程度,Masson三色染色法检测纤维化程度。TUNEL细胞凋亡试剂盒检测肺上皮细胞凋亡,免疫组化法及Western blot检测IL-33、α-平滑肌肌动蛋白(α-SMA)和上皮型钙粘蛋白(E-cad)的动态表达。结果与对照组比较,在肺纤维化过程中,BLM组E-cad的表达量在第14、28天均明显下降,IL-33的表达在第3、7、14天明显增加,α-SMA的表达在第3、7、14、28天明显升高(P“,”Objective To explore the expression of IL-33 in mice with pulmonary fibrosis.Methods Fourty mice were equally assigned into two groups.An acute pulmonary fibrosis model in group A was established by endotracheal bloemycin challenge once.The mice in group B were given normal saline as the controls.HE staining was performed to evaluate pulmonary inflammation.Masson′s trichrome was used to detect collagen.TUNEL apoptosis assay kit was used to detect epithelial apoptosis.Western blot and immunohistochemical analysis were adopted to detect the expressions of IL-33,E-cadherin and α-smooth muscle actin(α-SMA).Results Compared to group B,in group A,the expression of E-cadherin was lower on the 14thand 28th day(P<0.05),the expression of α-SMA was higher on the 3rd,7th,14th and 28th day(P<0.05),and the expression of IL-33 was higher on the 3rd,7th and 14th day(P<0.05).The cell apoptosis in group A peaked on the 7th day.Conclusion The abnormal apoptosis of epithelial and proliferation of fibroblasts occur during the development of pulmonary fibrosis,which is accompanied by dynamic expression of IL-33.