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YKL-40在肺纤维化大鼠中的动态表达
黄海东,宁允叶,李强*
0
(第二军医大学长海医院呼吸内科,上海 200433
*通信作者)
摘要:
目的 观察YKL-40在博莱霉素诱导的肺间质纤维化大鼠肺组织中的表达。方法 以博莱霉素(7.5 mg/kg体质量)气管内注入复制大鼠肺纤维化模型,对照组气管内注入等体积生理盐水。分别于第7天、第14天、第21天分批处死大鼠。通过H-E染色、Masson染色,并依据Szapiel评分方法 判断肺组织肺泡炎及肺纤维化程度,采用免疫组化、real-time RT-PCR及蛋白质印迹分析测定肺组织YKL-40的表达。 结果 博莱霉素组大鼠肺组织第7天肺泡炎程度(2.8±0.45)与对照组(0.42±0.25)相比差异有统计学意义(P<0.01),之后肺泡炎症减轻,但至第21天(1.8±0.84)与对照组间差异仍有统计学意义(P<0.05);肺组织纤维化程度在第14天(1.7±0.73)即与对照组(0.2±0.45)相比差异有统计学意义(P<0.05),至第21天(2.9±0.56)与对照组间差异有统计学意义(P<0.01)。YKL-40 mRNA相对表达量在第7天(3.71±0.25)即高于对照组(P<0.05);蛋白质印迹分析结果 显示,蛋白水平第14天(0.56±0.24)高于对照组(0.23±0.07,P<0.05),第21天(1.15±0.19)与对照组相比差异有统计学意义(P<0.01)。免疫组化结果 显示,博莱霉素诱导大鼠肺组织YKL-40的上调表达呈时间依赖性,且主要来源于平滑肌细胞、肺泡巨噬细胞、肺泡上皮细胞及成纤维细胞。结论 随着大鼠肺纤维化进展,YKL-40表达增加。YKL-40可能参与肺纤维化过程。
关键词:  YKL-40  肺纤维化  博来霉素
DOI:10.3724/SP.J.1008.2012.038
投稿时间:2011-06-27修订日期:2011-12-07
基金项目:
Dynamic expression of pulmonary YKL-40 protein in rats with bleomycin-induced pulmonary fibrosis
HUANG Hai-dong,NING Yun-ye,LI Qiang*
(Department of Respiratory Medicine, Changhai Hospital, Second Military Medical University, Shanghai 200433, China
*Corresponding author.)
Abstract:
Objective To observe the expression of YKL-40 protein in the pulmonary tissues of rats with bleomycin-induced pulmonary fibrosis(PF). MethodsThe PF model group was induced with intratracheal instillation of bleomycin solution (7.5 mg/kg) and the control group was treated with normal saline. On day 7, 14, 21 after bleomycin challenge, rats were sacrificed and the pulmonary tissues were harvested. H-E staining, Masson staining and Szapiel score were employed to determine alveolitis and pulmonary fibrosis. Expressions of YKL-40 in lung tissues were detected by real-time RT-PCR, Western blotting analysis and immunohistochemistry method. ResultsBleomycin instillation induced alveolitis in the lung of rats, with inflammation score being significantly higher on day 7 (2.8±0.45, P<0.01) and on day 21 (1.8±0.84, P<0.05) compared with that of control group (0.42±0.25). Pulmonary fibrosis degrees in model group was significantly higher on day 14 (1.7±0.73, P<0.05) and on day 21 (2.9±0.56, P<0.01) compared with that of control group (0.2±0.45). YKL-40 mRNA (YKL-40/β-actin) expression was significantly increased on day 7 (3.71±0.25) after bleomycin treatment compared with the control group (P<0.05). Western blotting analysis showed that YKL-40 protein expression was significantly increased on day 14(0.56±0.24,P<0.05) and on day 21(1.15±0.19, P<0.01) after bleomycin treatment compared with the control group (0.23±0.07). The results of immunohistochemistry showed that bleomycin up-regulated YKL-40 expression in a time-dependent manner, and YKL-40 expression was mainly located in the smooth muscle cells, alveolar macrophages, alveolar epithelium and fibroblasts. ConclusionYKL-40 expression may contribute to the pulmonary fibrosis, and may participate in the pathogenesis of pulmonary fibrosis.
Key words:  YKL-40  pulmonary fibrosis  bleomycin