Literature DB >> 2447097

Kinetics of endosome acidification in mutant and wild-type Chinese hamster ovary cells.

D J Yamashiro1, F R Maxfield.   

Abstract

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.

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Year:  1987        PMID: 2447097      PMCID: PMC2114743          DOI: 10.1083/jcb.105.6.2713

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  33 in total

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Authors:  A N Lestas
Journal:  Br J Haematol       Date:  1976-03       Impact factor: 6.998

2.  Difference between the two iron-binding sites of transferrin.

Authors:  J V Princiotto; E J Zapolski
Journal:  Nature       Date:  1975-05-01       Impact factor: 49.962

3.  Fluorescence probe measurement of the intralysosomal pH in living cells and the perturbation of pH by various agents.

Authors:  S Ohkuma; B Poole
Journal:  Proc Natl Acad Sci U S A       Date:  1978-07       Impact factor: 11.205

4.  Internal pH and state of ATP in adrenergic chromaffin granules determined by 31P nuclear magnetic resonance spectroscopy.

Authors:  H B Pollard; H Shindo; C E Creutz; C J Pazoles; J S Cohen
Journal:  J Biol Chem       Date:  1979-02-25       Impact factor: 5.157

5.  Acidification of morphologically distinct endosomes in mutant and wild-type Chinese hamster ovary cells.

Authors:  D J Yamashiro; F R Maxfield
Journal:  J Cell Biol       Date:  1987-12       Impact factor: 10.539

6.  Rapid acidification of endocytic vesicles containing alpha 2-macroglobulin.

Authors:  B Tycko; F R Maxfield
Journal:  Cell       Date:  1982-03       Impact factor: 41.582

7.  Hydrogen ion buffers for biological research.

Authors:  N E Good; G D Winget; W Winter; T N Connolly; S Izawa; R M Singh
Journal:  Biochemistry       Date:  1966-02       Impact factor: 3.162

8.  Collection of insulin, EGF and alpha2-macroglobulin in the same patches on the surface of cultured fibroblasts and common internalization.

Authors:  F R Maxfield; J Schlessinger; Y Shechter; I Pastan; M C Willingham
Journal:  Cell       Date:  1978-08       Impact factor: 41.582

9.  alpha 2 Macroglobulin binding to the plasma membrane of cultured fibroblasts. Diffuse binding followed by clustering in coated regions.

Authors:  M C Willingham; F R Maxfield; I H Pastan
Journal:  J Cell Biol       Date:  1979-09       Impact factor: 10.539

10.  Effect of weak bases on the intralysosomal pH in mouse peritoneal macrophages.

Authors:  B Poole; S Ohkuma
Journal:  J Cell Biol       Date:  1981-09       Impact factor: 10.539

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  30 in total

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2.  A possible role for Na+,K+-ATPase in regulating ATP-dependent endosome acidification.

Authors:  R Fuchs; S Schmid; I Mellman
Journal:  Proc Natl Acad Sci U S A       Date:  1989-01       Impact factor: 11.205

Review 3.  Pharmacokinetics, pharmacodynamics and physiologically-based pharmacokinetic modelling of monoclonal antibodies.

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4.  Acidification of morphologically distinct endosomes in mutant and wild-type Chinese hamster ovary cells.

Authors:  D J Yamashiro; F R Maxfield
Journal:  J Cell Biol       Date:  1987-12       Impact factor: 10.539

5.  mTORC1 signals from late endosomes: taking a TOR of the endocytic system.

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Journal:  Cell Cycle       Date:  2010-05-15       Impact factor: 4.534

Review 6.  Role of endosomes and lysosomes in human disease.

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Journal:  Cold Spring Harb Perspect Biol       Date:  2014-05-01       Impact factor: 10.005

7.  Plasmin promotes foam cell formation by increasing macrophage catabolism of aggregated low-density lipoprotein.

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8.  Mechanism of cellular uptake of modified oligodeoxynucleotides containing methylphosphonate linkages.

Authors:  Y Shoji; S Akhtar; A Periasamy; B Herman; R L Juliano
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9.  The late endosome is essential for mTORC1 signaling.

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10.  Analysis of endocytic pathways in Drosophila cells reveals a conserved role for GBF1 in internalization via GEECs.

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