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作 者:黄炜 李欣 张鸽[3] 李素香[4] 付桂茹[4] 袁静冉[4]
机构地区:[1]河北省唐山市工人医院老年病科,063000 [2]河北省唐山市工人医院放射科,063000 [3]河北省唐山市工人医院风湿免疫科,063000 [4]华北煤炭医学院附属医院
出 处:《中国综合临床》2008年第11期1163-1165,共3页Clinical Medicine of China
基 金:河北省唐山市科学技术研究与发展计划(041346176)
摘 要:目的类风湿性关节炎(Rheumatoid arthrithis,RA)滑膜细胞体外原代培养并传代至第三代,定量分析三氧化二砷(arsenic trioxide,As2O3)对滑膜细胞凋亡诱导作用。方法双酶消化法体外传代人关节滑膜细胞,采用3代滑膜细胞;应用MTT、流式细胞术对RA滑膜细胞凋亡进行分析。结果①MTT法显示不同浓度的As2O3作用48h后,能够抑制RA滑膜细胞增殖,且在10~80μmol/L浓度范围内其抑制作用呈剂量依赖性。②流式细胞仪检测发现不同浓度的As2O3作用48h后,RA滑膜细胞发生不同比率凋亡,并且在10~80μmol/L浓度范围内其作用呈剂量依赖性。结论不同浓度的As2O3作用48h后RA滑膜细胞均发生凋亡并且呈剂量依赖性。Objective To investigate arsenic trioxide ( As2O3 )-mediated apoptosis of synovial cells in patients with rheumatoid arthritis (RA) through culturing the synoviocytes in vitro. Methods Primary synovial cells were cultured by means of two-enzymatic digestion and the third cells were adopted in this test. The cultured cells were defined by MTT and flow cytometry ( FCM ). Results Certain concentration of As2O3 could inhibit the viability of synoviocytes at 48 h by means of MTT,which was dose-dependent. Certain concentration of As2O3 could induce the apoptosis of synoviocytes pro rata at 48h by means of FCM ,which was dose-dependent within range of 10-80 μmol/L concentration. Conclusion Certain concentration of As2O3 following 48 h effect could induce the apoptosis of synoviocytes of RA,which is dose-dependent.
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