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作 者:陈显凌[1] 陈元仲[1] 黄慧芳[1] 陈荣[2] 陈小芳[1] 黄祖芳[2]
机构地区:[1]福建医科大学附属协和医院福建省血液病研究所,福建福州350001 [2]福建师范大学物理与光学学院,福建福州350007
出 处:《激光生物学报》2007年第5期572-575,共4页Acta Laser Biology Sinica
基 金:福建省科技厅基金项目(2004y020)
摘 要:目的:探讨ZnPcS2P2在K562细胞,HL-60细胞亚细胞结构中的精确定位,揭示光动力学疗法(photody-namic therapy,PDT)的作用机制。方法:将K562细胞,HL-60细胞与ZnPcS2P2共同孵育5 h。应用激光扫描共聚焦显微成像系统,选择特异性细胞器荧光探针(线粒体探针若丹明Rodanmine123、溶酶体探针LysoTrackerDND-26、内质网探针Dioc6(3)采用波形比较法对光敏剂进行亚细胞定位。结果:ZnPcS2P2在K562细胞,HL-60细胞中发出的荧光与负载的Rodanmine123、Lyso-TracKer DND-26、Dioc6(3)均有部分重叠,波形均有相似之处。ZnPc-S2P2在线粒体、溶酶体、内质网均有分布。结论:线粒体是ZnPcS2P2介导的PDT(ZnPcS2P2-PDT)光损伤的主要靶点,溶酶体、内质网也是ZnPcS2P2-PDT光损伤的靶点。Objective. To investigate the mechanism of a novel amphipathic photo sensitizer [ di-sulfonated di-phthalimidomethyl phthalocyanine zinc (ZnPcS2P2 )]-mediated photodynamic therapy (ZnPcSEPE-PDT) on K562 cells and HL60 cells. Methods: Laser scanning confocal microscopy was applied and three special organelle probes including Rhodamine123, Lys -oTracker DND-26 and Dioc6 (3) were selected to label mitochondria, lysosome and endoplasmic reticulum fluorescence images both of ZnPc-SEP2 and the three probes were collected through corresponding emission filters. Results: ZnPcSEP2 was located on mitochondria lysosome, endoplasmic reticulum. Conclusion: This study provides direct evidence that mitochondria, lysosome and endoplasmic reticulum play an important role in the apoptosis in K562 cells and HL60 cells induced by ZnPcSEP2- PDT.
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