Hirosako Kaori, Imasato Hiroshi, Hirota Yuko, Kuronita Toshio, Masuyama Naoko, Nishioka Misa, Umeda Atsushi, Fujita Hideaki, Himeno Masaru, Tanaka Yoshitaka
Division of Pharmaceutical Cell Biology, Graduate School of Pharmaceutical Sciences, Kyushu University, 3-1-1 Maidashi, Fukuoka 812-8582, Japan.
Biochem Biophys Res Commun. 2004 Apr 9;316(3):845-52. doi: 10.1016/j.bbrc.2004.02.119.
3-Methyladenine (3-MA), a well-known inhibitor of autophagic sequestration, can also prevent class III phosphatidylinositide (PI) 3-kinase activity, which is required for many processes in endosomal membrane trafficking. Although much is known about the effects of other PI 3-kinase inhibitors, such as wortmannin and LY294002, on endosomal membrane trafficking, little is known about those of 3-MA. Here we show that the treatment of cells with 3-MA results in a specific redistribution of the cation-independent mannose 6-phosphate/insulin-like growth factor II receptor (MPR300) from the trans-Golgi network (TGN) to early/recycling endosomal compartments containing internalized transferrin. Importantly, in contrast to wortmannin and LY294002, 3-MA did not cause the enlargement of late endosomal/lysosomal compartments. The results suggest that the effect of 3-MA is restricted to the retrieval of MPR300 from early/recycling endosomes.
3-甲基腺嘌呤(3-MA)是一种著名的自噬隔离抑制剂,它还能抑制III类磷脂酰肌醇(PI)3-激酶的活性,而这种活性是内体膜运输中许多过程所必需的。尽管人们对其他PI 3-激酶抑制剂(如渥曼青霉素和LY294002)对内体膜运输的影响了解很多,但对3-MA的影响却知之甚少。在此我们表明,用3-MA处理细胞会导致阳离子非依赖性甘露糖6-磷酸/胰岛素样生长因子II受体(MPR300)从反式高尔基体网络(TGN)特异性重新分布到含有内化转铁蛋白的早期/再循环内体区室。重要的是,与渥曼青霉素和LY294002不同,3-MA不会导致晚期内体/溶酶体区室增大。结果表明,3-MA的作用仅限于从早期/再循环内体中回收MPR300。