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作 者:朱兰[1] 梁永强[2] 马小兵[1] 王献华[1] 孙树勋[3]
机构地区:[1]华北煤炭医学院病理教研室,唐山063000 [2]华北煤炭医学院口腔系,唐山063000 [3]华北煤炭医学院基础医学部,唐山063000
出 处:《中华劳动卫生职业病杂志》2009年第7期395-399,共5页Chinese Journal of Industrial Hygiene and Occupational Diseases
基 金:河北省自然科学基金资助项目(C2008001007)
摘 要:目的探讨经SiO:刺激的肺泡巨噬细胞(AM)通过人胚肺成纤维细胞(HELF)对基质金属蛋白酶-1(MMP-1)及其抑制因子(TIMP-1)和Ⅲ型胶原表达的影响。方法收集矽肺患者AM,将其分为加入SiO2粉尘悬液的处理组和仅加入无血清培养液的对照组。培养18h后吸出培养上清。将原代培养的HELF分为4组:(1)处理组:加入经SiO2刺激的AM上清;(2)对照组:加入未经SiO2刺激的AM上清;(3)10%血清组:仅加入含体积分数为10%胎牛血清的DMEM;(4)空白对照组:仅加入含体积分数为3%胎牛血清的DMEM。4组均分别于6、12、18、24、36、48h取出细胞爬片,吸出上清,用免疫细胞化学方法检测HELF中MMP-1和TIMP-1的表达,用Western blot法检测HELF条件培养上清中Ⅲ型胶原的表达。结果处理组18、24、36、48hMMP-1表达分别为0.0605±0.0201,0.0519±0.0117,0.0412±0.0105,0.0213±0.0106,较对照组和空白对照组明显降低,差异均有统计学意义(P〈0.05,P〈0.01)。与对照组和空白对照组相比,处理组各时间点TIMP一1表达和Ⅲ型胶原含量明显增高,差异均有统计学意义(P〈0.05,P〈O.01),TIMP-1/MMP-1与Ⅲ型胶原呈正相关(r=0.88,19〈0.01)。结论SiO2经AM的介导可促进FB表达TIMP-1和Ⅲ型胶原,抑制HELF表达TIMP-1,TIMP-1/MMP-1的失衡与Ⅲ型胶原的病理性累积有关。Objective To study the effect of culture supernatant of alveolar macrophage alveolar macrophages(AM) stimulated by SiO2 on the expression of matrix metalloproteinases(MMP-1),tissue inhibitor of metalloproteinase-1 (TIMP-1) and collagen of fibroblast human embroyonic lung fibroblasts (HELF) in the development of silicosis fibrosis. Methods AMs were collected from a silicotic patient by bronchoalveolar lavage and exposed to SiO2, cultured human embryo lung fibroblast were allocated into a treated group, a control group, a positive group, and a blank group. HELF was incubated with the cultured supernatant of AMs for 6, 12, 18, 24, 36, 48 h. Immunocytochemical and Western blot technology were used to detect MMP-1 and TIMP-1 expressions in HELF and collagen expression in supernatant of HELF respectively. Results The supernatant of AM exposed to SiO2 significantly decreased the expressions of MMP-1 (0.0605±0.0201,0.0519± 0.0117, 0.0412±0.0105 and 0.0213±0.0106 in the treated group at 18, 24, 36 and 48 h) compared with the control group and the blank group (P〈0.05, P〈0.01 ) but stimulated expressions of TIMP-1 and collagen (P〈 0.05 ,P〈0.01 ). The ratio of TIMP-1 to MMP-1 increased. The ratio of TIMP-1 to MMP-1 was positively correlated with the expression of collagen m (r=0.88, P〈0.01 ). Conclusion Through AM mediation SiO2 can accelerate the expression of TIMP-1 and collagen, and inhibit the expression of MMP-1. The imbalance between the expression of TIMP-1 and that of MMP-1 is related with the abnormal increase in collagen Ⅲ.
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