Yamashiro D J, Maxfield F R
Department of Pharmacology, New York University School of Medicine, New York 10016.
J Cell Biol. 1987 Dec;105(6 Pt 1):2713-21. doi: 10.1083/jcb.105.6.2713.
Acidification of endocytic compartments is necessary for the proper sorting and processing of many ligands and their receptors. Robbins and co-workers have obtained Chinese hamster ovary (CHO) cell mutants that are pleiotropically defective in endocytosis and deficient in ATP-dependent acidification of endosomes isolated by density centrifugation (Robbins, A. R., S. S. Peng, and J. L. Marshall. 1983. J. Cell Biol. 96:1064-1071; Robbins, A. R., C. Oliver, J. L. Bateman, S. S. Krag, C. J. Galloway, and I. Mellman. 1984. J. Cell Biol. 99:1296-1308). In this and the following paper (Yamashiro, D. J., and F. R. Maxfield. 1987. J. Cell Biol. 105:2723-2733) we describe detailed studies of endosome acidification in the mutant and wild-type CHO cells. Here we describe a new microspectrofluorometry method based on changes in fluorescein fluorescence when all cellular compartments are equilibrated to the same pH value. Using this method we measured the pH of endocytic compartments during the first minutes of endocytosis. We found in wild-type CHO cells that after 3 min, fluorescein-labeled dextran (F-Dex) was in endosomes having an average pH of 6.3. By 10 min, both F-Dex and fluorescein-labeled alpha 2-macroglobulin (F-alpha 2M) had reached acidic endosomes having an average pH of 6.0 or below. In contrast, endosome acidification in the CHO mutants DTG 1-5-4 and DTF 1-5-1 was markedly slowed. The average endosomal pH after 5 min was 6.7 in both mutant cell lines. At least 15 min was required for F-Dex and F-alpha 2M to reach an average pH of 6.0 in DTG 1-5-4. Acidification of early endocytic compartments is defective in the CHO mutants DTG 1-5-4 and DTF 1-5-1, but pH regulation of later compartments on both the recycling pathway and lysosomal pathway is nearly normal. The properties of the mutant cells suggest that proper functioning of pH regulatory mechanisms in early endocytic compartments is critical for many pH-mediated processes of endocytosis.
内吞小室的酸化对于许多配体及其受体的正确分选和加工是必需的。罗宾斯及其同事获得了中国仓鼠卵巢(CHO)细胞突变体,这些突变体在内吞作用方面存在多效性缺陷,并且通过密度离心分离的内体中依赖ATP的酸化作用不足(罗宾斯,A.R.,S.S.彭和J.L.马歇尔。1983年。《细胞生物学杂志》96:1064 - 1071;罗宾斯,A.R.,C.奥利弗,J.L.贝特曼,S.S.克拉格,C.J.加洛韦和I.梅尔曼。1984年。《细胞生物学杂志》99:1296 - 1308)。在本文以及随后的论文(山代史郎,D.J.和F.R.马克斯菲尔德。1987年。《细胞生物学杂志》105:2723 - 2733)中,我们描述了对突变型和野生型CHO细胞内体酸化的详细研究。在这里,我们描述了一种新的显微分光荧光测定法,该方法基于当所有细胞区室平衡到相同pH值时荧光素荧光的变化。使用这种方法,我们在胞吞作用的最初几分钟内测量了内吞小室的pH值。我们发现在野生型CHO细胞中,3分钟后,荧光素标记的葡聚糖(F - Dex)存在于平均pH值为6.3的内体中。到10分钟时,F - Dex和荧光素标记的α2 - 巨球蛋白(F - α2M)都到达了平均pH值为6.0或更低的酸性内体中。相比之下,CHO突变体DTG 1 - 5 - 4和DTF 1 - 5 - 1中的内体酸化明显减慢。在这两种突变细胞系中,5分钟后的平均内体pH值为6.7。在DTG 1 - 5 - 4中,F - Dex和F - α2M至少需要15分钟才能达到平均pH值6.0。早期内吞小室的酸化在CHO突变体DTG 1 - 5 - 4和DTF 1 - 5 - 1中存在缺陷,但在回收途径和溶酶体途径上后期区室的pH调节几乎正常。突变细胞的特性表明,早期内吞小室中pH调节机制的正常运作对于许多pH介导的内吞过程至关重要。