Luna M C, Ferrario A, Rucker N, Gomer C J
Clayton Ocular Oncology Center, Childrens Hospital Los Angeles 90027, USA.
Cancer Res. 1995 May 1;55(9):1820-3.
Parental and photodynamic therapy (PDT)-resistant mouse, radiation-induced fibrosarcoma cell lines were evaluated using mRNA differential display in an attempt to identify unique transcripts. We detected one transcript that was consistently present in the parental cells but absent in PDT-resistant cells. The transcript was cloned, sequenced, and identified as alpha-2 macroglobulin receptor/low density lipoprotein receptor-related protein (alpha-2 MR/LRP). Northern and Western immunoblot analysis confirmed that receptor expression was present in the parental cell line but barely detectable in PDT-resistant cells. Functionality of the receptor was evaluated by exposing cells to Pseudomonas exotoxin A. alpha-2 MR/LRP is responsible for Pseudomonas exotoxin A internalization, and only the parental cells exhibited toxin-mediated cytotoxicity. The binding and endocytosis of activated alpha-2 macroglobulin and lipoproteins by alpha-2 MR/LRP are consistent with modulating uptake and localization of photosensitizers. Our results demonstrate that PDT-resistant murine tumor cells exhibit minimal alpha-2 MR/LRP activity and suggest that this receptor plays a role in PDT sensitivity by modulating photosensitizer uptake and/or subcellular localization.
使用mRNA差异显示技术对亲本及耐光动力疗法(PDT)的小鼠辐射诱导纤维肉瘤细胞系进行评估,以试图鉴定独特的转录本。我们检测到一个转录本,它在亲本细胞中始终存在,但在耐PDT细胞中不存在。该转录本被克隆、测序,并鉴定为α-2巨球蛋白受体/低密度脂蛋白受体相关蛋白(α-2 MR/LRP)。Northern印迹和Western免疫印迹分析证实,该受体在亲本细胞系中存在表达,但在耐PDT细胞中几乎检测不到。通过将细胞暴露于铜绿假单胞菌外毒素A来评估该受体的功能。α-2 MR/LRP负责铜绿假单胞菌外毒素A的内化,并且只有亲本细胞表现出毒素介导的细胞毒性。α-2 MR/LRP对活化的α-2巨球蛋白和脂蛋白的结合及内吞作用与调节光敏剂的摄取和定位一致。我们的结果表明,耐PDT的小鼠肿瘤细胞表现出最小的α-2 MR/LRP活性,并提示该受体通过调节光敏剂摄取和/或亚细胞定位在PDT敏感性中发挥作用。