Abstract

Endocytic vesicles possess an electrogenic proton pump, and measurements of ATPase activity suggest that Cl- may stimulate proton pump activity. This study was undertaken to measure the steady-state pH, potential (delta psi), and total proton electrochemical gradients established by the rat liver multivesicular body (MVB) proton pump and to examine the effects of Cl- (0.5-140 mM) on these gradients. Radiolabeled [( 14C] methylamine and 36Cl-) and fluorescent (fluorescein isothiocyanate-conjugated low density lipoproteins) probes were used to assess internal pH (pHi) and delta psi. In the absence of ATP, pHi averaged 7.37 +/- 0.05 (extracellular pH 7.31 +/- 0.02), and delta psi ranged from -32 to -71 mV; but neither pHi nor delta psi varied consistently with [Cl-]. In the presence of ATP, pHi decreased progressively with increasing [Cl-] to a plateau value of about 5.89 at greater than or equal to 25 mM Cl-, and MVB exhibited an interior positive delta psi that was maximal at the lowest Cl- concentration (+65.5 mV) and decreased as medium Cl- increased. The total ATP-dependent proton electrochemical gradient (proton-motive force (delta p] averaged 118.0 +/- 4.3 mV and did not change in any consistent manner as [Cl-] varied almost 300-fold. However, initial rates of MVB acidification increased with increasing [Cl-]. These studies indicate that: (a) in the absence of ATP, isolated MVB exhibited a negative delta psi, probably a Donnan potential; (b) in the presence of ATP and at a [Cl-] similar to that in hepatocyte cytoplasm (25 mM), MVB pHi was 5.89, and delta psi was +9.6 mV; and (c) over the range of [Cl-] tested, the magnitudes of delta pH and delta psi were inversely related, apparently related to Cl- availability, but the ATP-dependent delta p did not vary. Therefore, it is concluded that Cl- increases the initial rate of vesicle acidification in MVB and also affects the relative chemical and electrical contributions of the steady-state proton pump-determined delta p. Cl-, however, does not alter steady-state delta p.

Highlights

  • From the Department of Medicine and the Liver Center, Universityof California Medical Center, San Francisco, Californ$94143

  • Endocytic vesicles possess an electrogenicproton (MVB),’as well as a wide variety of intracellular organelles pump, and measurements of ATPase activity suggest in animal and planctells [1,2,3,4], contain an electrogenicproton that C1- may stimulateproton pump activity.This study was undertaken to measure the steady-staptHe, potential (A$), and total proton electrochemical gradients established by the rat liver multivesicular body (MVB) proton pump and to examine the effectosfC1(0.5-140 mM) on these gradients

  • MVB loaded with FITC-LDL were placed in 2 ml of medium (pH, 7.19 +: 0.04; n = 91, identical to thatused for proton pump-generated ApH, A+, and total electrochemical ["Clmethylamine uptake studies, in plastic cuvettes in a temperatureproton (proton-motive force (Ap))gradients a t steady state in rat liver multivesicular bodies, to determine the values for these gradients that might be expected under in uiuo conditions, and to examine the effects of C1- on them

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Summary

QUANTITATION AND EFFECTS OF CHLORIDE*

MVB loaded with FITC-LDL were placed in 2 ml of medium (pH, 7.19 +: 0.04; n = 91, identical to thatused for proton pump-generated ApH, A+, and total electrochemical ["Clmethylamine uptake studies, in plastic cuvettes in a temperatureproton (proton-motive force (Ap))gradients a t steady state in rat liver multivesicular bodies, to determine the values for these gradients that might be expected under in uiuo conditions, and to examine the effects of C1- on them. MVB, MgATP, isotope, and incubation medium together in 2 ml of were loaded with FITC-LDL as described under "Experimental Proice-cold stop solution and filtering immediately, were determined for cedures." 0.8 mg of MVB were placed in a cuvette containing 2 ml of each experiment; and all uptake data were corrected by subtraction medium (140 mM potassium salt, 40 mM HEPES (pH 7.2), and an of the appropriate blank values.

Initial rates of fluorescence quenching were also calculated from the
RESULTS
No ATP
DISCUSSION
Full Text
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