|
||
The Journal of General Physiology, Vol 85, 443-470, Copyright © 1985 by The Rockefeller University Press
ARTICLES |
L Simchowitz and A Roos
The intracellular pH (pHi) of isolated human peripheral blood neutrophils was measured from the fluorescence of 6-carboxyfluorescein (6-CF) and from the equilibrium distribution of [14C]5,5- dimethyloxazolidine -2,4-dione (DMO). At an extracellular pH (pHo) of 7.40 in nominally CO2-free medium, the steady state pHi using either indicator was approximately 7.25. When pHo was suddenly raised from 7.40 to 8.40 in the nominal absence of CO2, pHi slowly rose by approximately 0.35 during the subsequent hour. A change of similar magnitude in the opposite direction occurred when pHo was reduced to 6.40. Both changes were reversible. Intrinsic intracellular buffering power, determined by using graded pulses of CO2 or NH4Cl, was approximately 50 mM/pH over the pHi range of 6.8-7.9. The course of pHi obtained from the distribution of DMO was followed during and after imposition of intracellular acid and alkaline loads. Intracellular acidification was brought about either by exposing cells to 18% CO2 or by prepulsing with 30 mM NH4Cl, while pHo was maintained at 7.40. In both instances, pHi (6.80 and 6.45, respectively) recovered toward the control value at rates of 0.029 and 0.134 pH/min. These rates were reduced by approximately 90% either by 1 mM amiloride or by replacement of extracellular Na with N-methyl-D-glucamine. Recovery was not affected by 1 mM SITS or by 40 mM alpha-cyano-4-hydroxycinnamate (CHC), which inhibits anion exchange in neutrophils. Therefore, recovery from acid loading is probably due to an exchange of internal H for external Na. Intracellular alkalinization was achieved by exposing the cells to 30 mM NH4Cl or by prepulsing with 18% CO2, both at a constant pHo 7.40. In both instances, pHi, which was 7.65 and 7.76, respectively, recovered to the control value. The recovery rates (0.033 and 0.077 pH/min, respectively) were reduced by 80-90% either by 40 mM CHC or by replacement of extracellular Cl with p-aminohippurate (PAH). SITS, amiloride, and ouabain (0.1 mM) were ineffective.(ABSTRACT TRUNCATED AT 400 WORDS)
This article has been cited by other articles:
![]() |
N. K. Kaba, J. Schultz, F.-Y. Law, C. T. Lefort, G. Martel-Gallegos, M. Kim, R. E. Waugh, J. Arreola, and P. A. Knauf Inhibition of Na+/H+ exchanger enhances low pH-induced L-selectin shedding and {beta}2-integrin surface expression in human neutrophils Am J Physiol Cell Physiol, November 1, 2008; 295(5): C1454 - C1463. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. M. Herrmann, J. Bernardo, H. J. Long, K. Seetoo, M. E. McMenamin, E. L. Batista Jr., T. E. Van Dyke, and E. R. Simons Sequential Chemotactic and Phagocytic Activation of Human Polymorphonuclear Neutrophils Infect. Immun., August 1, 2007; 75(8): 3989 - 3998. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. Zhou, J. Zhao, P. Bouyer, and W. F. Boron Evidence from renal proximal tubules that HCO3 and solute reabsorption are acutely regulated not by pH but by basolateral HCO3 and CO2 PNAS, March 8, 2005; 102(10): 3875 - 3880. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Zhao, Y. Zhou, and W. F. Boron Effect of isolated removal of either basolateral HCO-3 or basolateral CO2 on HCO-3 reabsorption by rabbit S2 proximal tubule Am J Physiol Renal Physiol, August 1, 2003; 285(2): F359 - F369. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. E. Decoursey Voltage-Gated Proton Channels and Other Proton Transfer Pathways Physiol Rev, April 1, 2003; 83(2): 475 - 579. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. J. Coakley, C. Taggart, N. G. McElvaney, and S. J. O'Neill Cytosolic pH and the inflammatory microenvironment modulate cell death in human neutrophils after phagocytosis Blood, October 16, 2002; 100(9): 3383 - 3391. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. J. Coakley, C Taggart, C Greene, N. G McElvaney, and S. J. O'Neill Ambient pCO2 modulates intracellular pH, intracellular oxidant generation, and interleukin-8 secretion in human neutrophils J. Leukoc. Biol., April 1, 2002; 71(4): 603 - 610. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Menegazzi, S. Busetto, R. Cramer, P. Dri, and P. Patriarca Role of Intracellular Chloride in the Reversible Activation of Neutrophil {beta}2 Integrins: A Lesson from TNF Stimulation J. Immunol., October 15, 2000; 165(8): 4606 - 4614. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. J. Coakley, C. Taggart, G. Canny, P. Greally, S. J. O'Neill, and N. G. McElvaney Altered intracellular pH regulation in neutrophils from patients with cystic fibrosis Am J Physiol Lung Cell Mol Physiol, July 1, 2000; 279(1): L66 - L74. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. S. Trevani, G. Andonegui, M. Giordano, D. H. Lopez, R. Gamberale, F. Minucci, and J. R. Geffner Extracellular Acidification Induces Human Neutrophil Activation J. Immunol., April 15, 1999; 162(8): 4849 - 4857. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. C. C. de Hurtado, B. V. Alvarez, N. G. Perez, I. L. Ennis, and H. E. Cingolani Angiotensin II Activates Na+-Independent Cl--HCO3- Exchange in Ventricular Myocardium Circ. Res., March 9, 1998; 82(4): 473 - 481. [Abstract] [Full Text] [PDF] |
||||
![]() |
I Yuli and A Oplatka Cytosolic acidification as an early transductory signal of human neutrophil chemotaxis Science, January 16, 1987; 235(4786): 340 - 342. [Abstract] [PDF] |
||||
|
|