期刊文献+

部花青(MC540)介导的光敏作用体外净化自体骨髓移植物的实验研究 被引量:2

EXPERIMENTAL STUDY ON PURGING AUTOLOGOUS BONE MARROW GRAFTS IN VITRO BY MC540-MEDIATED PHOTOSENSITIZATION
原文传递
导出
摘要 用氩离子激光(波长514nm)照射,部花青(MC540)介导的光敏作用对白血病细胞系HL-60、K562,急性髓细胞白血病原代祖细胞(CFU-L)以及正常骨髓CFU-GM的杀伤敏感性作了比较;用电镜观察处理前后K562细胞的超微结构变化。单纯激光照射或仅有MC540而不照光,对HL-60细胞集落产率及CFU-GM产率无明显影响。当MC540浓度为25μg/ml、激光照射能量密度为79.51/cm ̄2的条件处理,HL-60集落产率下降2.8个对数级、CFU-L减少2.2个对数级,而骨贿CFU-GM尚能保留64.0±7.0%;含1%K562细胞的模拟白血病骨贿经同样处理,K562集落产率能下降1.36对数级,而CFU-GM尚存74.0±19.0%。电镜观察发现处理后的K562细胞体积增大,肿胀,胞膜洞孔样破坏。结果提示,氩离子激光照射,MC540介导的光敏作用能选择性杀伤白血病细胞系,原代白血病祖细胞同样敏感。其对细胞的杀伤作用可能主要因直接造成胞膜破坏。该方法将可能成为一种有前途的自体骨髓移植物体外净化手段。 he purpose of this study was to determine the sensi-tivity to argon ion laser-induced merocyanine 540(MC540)- mediated photolysis of leukemic cells and nor-mal marrow CFU-GM. HL-60 cells ,marrow cells of acute myelogenous leukemia ( AML),simulatedleukemic marrow cells with 1%occulted K562 cells,andnormal marrow cells were incubated respectively withMC540(25μg/ml) in the presence of 15%newborn calfserum and simutaneously exposed to 79.5J/cm ̄2 laser ir-radiation. The results showed that 2. 8 log of HL-60 cellcolonies and 2.2 log of CFU-L were killed respectively,whereas 64.0±7.0%of CFU-GM survived. In simulat-ed leukemic marrow,K562 colonies were reduced by1. 36 log while 74.0±19.0%of CFU-GM remained.There was no significant reduction in HL-60 colonies orCFU-GM when HL- 60 cells or marrow cells were ex-posed to laser light alone or incubated with MC540 inthe dark.A damaged membrane with various size holeswas observed in K5 6 2 cells after MC540-mediated pho-tosensitization.The results indicated that MC540-medi-ated photosensitization has selective cytotoxic effect onleukemic cells and it might be promising for purging au-tologous bone marrow grafts in vitro.
出处 《中华血液学杂志》 CAS CSCD 北大核心 1994年第6期304-307,共4页 Chinese Journal of Hematology
关键词 部花青 光敏作用 骨髓净化 白血病 Merocyanine 540(MC540)Photo-sensitization Bone marrow purging
  • 相关文献

同被引文献11

引证文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部