Segregation of transferrin to a mildly acidic (pH 6.5) para-golgi compartment in the recycling pathway
To study the intracellular sorting of internalized ligands and receptors, we examined the pathways of two ligands: transferrin, which is recycled, and α 2-macroglobulin ( α 2M), which is degraded. In CHO cells the two ligands rapidly segregate into different intracellular compartments. Within 5 min...
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Veröffentlicht in: | Cell 1984-07, Vol.37 (3), p.789-800 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | To study the intracellular sorting of internalized ligands and receptors, we examined the pathways of two ligands: transferrin, which is recycled, and
α
2-macroglobulin (
α
2M), which is degraded. In CHO cells the two ligands rapidly segregate into different intracellular compartments. Within 5 min fluorescein-labeled transferrin (F-Tf) is found in a large round juxtanuclear structure. Rhodamine-labeled
α
2M is found in a punctate pattern. Ultra-structural localization studies demonstrate that colloidal gold-
α
2M is found predominantly in endocytic vesicles, while ferritin-transferrin is found in small vesicles and tubular structures in a region adjacent to the Golgi complex. Using image intensified fluorescence microscopy and digital image analysis, we determined that the F-Tf containing structure has a pH of 6.4 ± 0.2, while endocytic vesicles containing F-
α
2M have a pH of 5.4 ± 0.1. Our study defines a mildly acidic compartment, distinct from endocytic vesicles, that is involved in the recycling of internalized components back to the cell surface. |
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ISSN: | 0092-8674 1097-4172 |
DOI: | 10.1016/0092-8674(84)90414-8 |