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机构地区:[1]南华大学附属第一医院皮肤科,湖南衡阳421001 [2]广东省江门市皮肤病防治所
出 处:《中华皮肤科杂志》2009年第2期105-107,共3页Chinese Journal of Dermatology
基 金:基金项目:湖南省医药卫生科研计划项目(B2007099);衡阳市科技发展项目(2007KJ017)
摘 要:目的探讨内皮素(ET)-1对人A375黑素瘤细胞增殖、黏附、迁移及细胞黏附分子(ICAM)-l表达的影响。方法MTT法观察ET-1对人A375黑素瘤细胞生长的影响,黏附实验检测细胞黏附,Transwell迁移系统检测细胞迁移,流式细胞仪检测对人A375黑素瘤细胞ICAM-1表达的影响。结果ET-1在0.002~0.2μg/mL浓度范围可促进黑素瘤细胞的增殖、在纤连蛋白上的黏附、通过微孔滤膜及抑制ICAM—1的表达(P〈0.01),在0.2μg/mL时作用最强,细胞代谢活性(24h)、细胞黏附率、ICAM-1含量(24h)分别为0.327±0.009、163.31±4.05、4.667±0.551;在0.2~2μg/mL浓度范围作用相反。结论ET-1可能通过抑制ICAM—1的表达、促进细胞增殖、黏附及迁移而增强细胞代谢、增加色素形成。Objective To observe the effect of endothelin-1 (ET-1) on the cell growth, adhesion, migration and expression of intercellular adhesion molecule 1 (ICAM-1) by A375 human malignant melanoma cells. Methods A375 cells were cultured in the presence of ET-1 of various concentrations (0.002, 0.02, 0.2, 2 μg/mL) for different periods. MTT method and flow cytometry were applied to detect the proliferation and ICAM-1 expression of these cells, respectively, after 24-, 48-, and 72-hour treatment. After 24-hour treatment, the cell adhesion and migration of A375 cells were assessed with cell adhesion assay and Transwell chambers, respectively. Results In the case of ET-1 from 0.002 to 0.2 μg/mL, it enhanced the proliferation, adhesion, migration of A375 cells and inhibited the expression of ICAM-1 by A375 cells in a dose dependent manner (P 〈 0.01 or 〈 0.05); however, for ET-1 of 2 μg/mL, the situation was the opposite. Moreover, after 24-hour culture with ET-1 of 0.2 μg/mL, the metabolic activity, cell adhesion rate, and expression of ICAM-1 peaked at 0.327 ± 0.009, (163.31±4.05)% and 4.667 ±0.551, respectively. Conclusion ET-1 may enhance cellular metabolism and pigmentation by suppressing the expression of ICAM-1 and promoting the proliferation, adhesion and migration of melanoma cells.
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