Hirota Yuko, Masuyama Naoko, Kuronita Toshio, Fujita Hideaki, Himeno Masaru, Tanaka Yoshitaka
Division of Pharmaceutical Cell Biology, Graduate School of Pharmaceutical Sciences, Kyushu University, 3-1-1 Maidashi, 812-8582 Fukuoka, Japan.
Biochem Biophys Res Commun. 2004 Feb 6;314(2):306-12. doi: 10.1016/j.bbrc.2003.12.092.
Lysosomes are acidic intracellular compartments and are regarded as degradative and the end point, of the endocytic pathway. Here we provide evidence for the generation of acid hydrolase poor and non-acidic post-lysosomal compartments in NRK cells that have accumulated non-digestible macromolecules, Texas red-dextran (TR-Dex), within lysosomes. When TR-Dex was fed to the cells for 6h, most of the internalized TR-Dex colocalized with a lysosomal enzyme, cathepsin D. With an increase in the chase period, however, the internalized TR-Dex gradually accumulated in cathepsin D-negative vesicles. These vesicles were positive for a lysosomal membrane protein, LGP85, and their formation was inhibited by treatment of the cells with U18666A, which impairs membrane transport out of late endosomal/lysosomal compartments, thereby suggesting that the vesicles are derived from lysosomes. Interestingly, these compartments are non-acidic as judged for the DAMP staining. The results, therefore, suggest that the excess accumulation of non-digestible macromolecules within lysosomes induces the formation of acid hydrolase poor and non-acidic post-lysosomal compartments. The fact that treatment of the cells with lysosomotropic amines or a microtubule-depolymerization agent resulted in extensive colocalization of TR-Dex with cathepsin D further indicates that the formation of the post-lysosomal compartments depends on the lysosomal acidification and microtubule organization. Furthermore, these results suggest bi-directional membrane transport between lysosomes and the post-lysosomal compartments, which implies that the latter are not resting compartments.
溶酶体是酸性的细胞内区室,被视为内吞途径的降解终点。在这里,我们提供证据表明,在已在溶酶体内积累了不可消化大分子(德克萨斯红-葡聚糖,TR-Dex)的NRK细胞中,会生成酸性水解酶含量低且非酸性的溶酶体后区室。当将TR-Dex加入细胞中6小时时,大多数内化的TR-Dex与溶酶体酶组织蛋白酶D共定位。然而,随着追踪时间的增加,内化的TR-Dex逐渐在组织蛋白酶D阴性囊泡中积累。这些囊泡对溶酶体膜蛋白LGP85呈阳性,并且用U18666A处理细胞会抑制它们的形成,U18666A会损害从晚期内体/溶酶体区室的膜转运,从而表明这些囊泡源自溶酶体。有趣的是,根据DAMP染色判断,这些区室是非酸性的。因此,结果表明溶酶体内不可消化大分子的过量积累会诱导酸性水解酶含量低且非酸性的溶酶体后区室的形成。用溶酶体促渗胺或微管解聚剂处理细胞会导致TR-Dex与组织蛋白酶D广泛共定位,这一事实进一步表明溶酶体后区室的形成取决于溶酶体酸化和微管组织。此外,这些结果表明溶酶体与溶酶体后区室之间存在双向膜转运,这意味着后者不是静止区室。