Acidification of three types of liver endocytic vesicles: Similarities and differences

R. W. Van Dyke, J. D. Belcher

Research output: Contribution to journalArticle

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Abstract

Endocytosed ligands move through a series of progressively more acidic vesicles. These differences in pH (pH(i)) could reflect differences in ion transport mechanisms. Vesicles representing three stages of endocytosis, compartment for uncoupling of receptor and ligand (CURL), multivesicular bodies (MVB), and receptor recycling compartment (RRC), were studied, and all exhibited ATP-dependent electrogenic acidification that was a saturable function of medium chloride. Initial rates of acidification differed (RRC > CURL > MVB), and proton influx was similar for CURL and RRC but slower for MVB. Steady-state ATP-dependent pH(i) in the three vesicles was more similar. Vesicle membrane potential was substantial (+41 to +69 mV) in low-chloride medium and greatest for RRC but was low (-6 to +6 mV) in 140 mM KCl. These vesicles also exhibited -22 to -37 mV Donnan potentials. Steady-state pump- generated proton electrochemical gradients (Δμ̄(H+)) ranged from 114 to 175 mV and were greater for CURL and RRC than for MVB; however, Δμ̄(H+) changed little over a 140-fold difference in chloride concentration. Proton leak rates were faster in CURL and RRC than in MVB, but proton efflux was similar. Finally, proton fluxes and permeabilities, calculated with regard to surface area, differed in the opposite direction (MVB > CURL > RRC). Thus, for the endocytic vesicles studied, intrinsic differences in proton flux and in vesicle geometry could be demonstrated that contributed to differences in pre-steady-state vesicle pH(i).

Original languageEnglish (US)
Pages (from-to)C81-C94
JournalAmerican Journal of Physiology - Cell Physiology
Volume266
Issue number1 35-1
DOIs
StatePublished - 1994

Keywords

  • compartment for uncoupling of receptor and ligand
  • endosomes
  • multivesicular bodies
  • proton permeability
  • proton-translocating adenosinetriphosphatase

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