Am J Physiol Cell Physiol AJP: Lung Cellular and Molecular Physiology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am J Physiol Cell Physiol 259: C819-C827, 1990;
0363-6143/90 $5.00
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Payne, J. A.
Right arrow Articles by McManus, T. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Payne, J. A.
Right arrow Articles by McManus, T. J.

AJP - Cell Physiology, Vol 259, Issue 5 C819-C827, Copyright © 1990 by American Physiological Society


ARTICLES

Foreign anion substitution for chloride in human red blood cells: effect on ionic and osmotic equilibria

J. A. Payne, C. Lytle and T. J. McManus
Department of Physiology, Duke University Medical Center, Durham, North Carolina 27710.

In human red blood cells, when chloride was replaced isosmotically with a permeant chaotropic anion of the lyotropic series (NO3, I, or SCN), an immediate and significant loss of cell water was observed. In contrast, replacement of chloride by a substituted monovalent sulfonate, such as methanesulfonate or sulfamate, had no significant effect on cell water. Cell water loss in the presence of lyotropic anions was not the result of hemolysis or cation loss but was associated with a significant fall in the distribution ratios of protons (out/in) and chloride (in/out), suggesting an increase in nondiffusible intracellular negative charges. This hypothesis was examined using the equilibrium dialysis technique of Freedman and Hoffman (J. Gen. Physiol. 74: 157-185, 1979) in which fixed charges are titrated in cells permeabilized by nystatin. The equilibrium concentration ratios (in/out) of potassium, sodium, and chloride were determined at various external pH (pHo) values. The point at which anion and cation ratios are equal is the effective isoelectric point for the intracellular charges. In normal chloride-containing medium at 24 degrees C, this point was found at a pHo of 6.93. When chloride was replaced by a chaotropic anion, the isoelectric point at 24 degrees C shifted to a lower pHo: NO3 (6.38), I (5.98), and SCN (5.70). The substituted monovalent sulfonates had little effect on isoelectric point: methyl sulfate (6.81), sulfamate (7.00), and methanesulfonate (7.07). Calculation of the intracellular charges from titration data, as well as equilibrium distribution studies with [14C]SCN, suggests that lyotropic anion binding to intracellular sites (mainly hemoglobin) is responsible for the observed changes in cell water, cell pH, and chloride distribution.


This article has been cited by other articles:


Home page
Am. J. Physiol. Cell Physiol.Home page
C. Lytle and T. McManus
Coordinate modulation of Na-K-2Cl cotransport and K-Cl cotransport by cell volume and chloride
Am J Physiol Cell Physiol, November 1, 2002; 283(5): C1422 - C1431.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
A. Mercado, P. de los Heros, N. Vazquez, P. Meade, D. B. Mount, and G. Gamba
Functional and molecular characterization of the K-Cl cotransporter of Xenopus laevis oocytes
Am J Physiol Cell Physiol, August 1, 2001; 281(2): C670 - C680.
[Abstract] [Full Text] [PDF]


Home page
J. Appl. Physiol.Home page
H. D. Prange, J. L. Shoemaker Jr., E. A. Westen, D. G. Horstkotte, and B. Pinshow
Physiological consequences of oxygen-dependent chloride binding to hemoglobin
J Appl Physiol, July 1, 2001; 91(1): 33 - 38.
[Abstract] [Full Text] [PDF]


Home page
Physiol. Rev.Home page
K. Kirk
Membrane Transport in the Malaria-Infected Erythrocyte
Physiol Rev, April 1, 2001; 81(2): 495 - 537.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
I. Bize, B. Guvenc, A. Robb, G. Buchbinder, and C. Brugnara
Serine/threonine protein phosphatases and regulation of K-Cl cotransport in human erythrocytes
Am J Physiol Cell Physiol, November 1, 1999; 277(5): C926 - C936.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
L. K. Putney, C. R. T. Vibat, and M. E. O'Donnell
Intracellular Cl regulates Na-K-Cl cotransport activity in human trabecular meshwork cells
Am J Physiol Cell Physiol, September 1, 1999; 277(3): C373 - C383.
[Abstract] [Full Text] [PDF]


Home page
BloodHome page
R. S. Schwartz, S. Musto, M. E. Fabry, and R. L. Nagel
Two Distinct Pathways Mediate the Formation of Intermediate Density Cells and Hyperdense Cells From Normal Density Sickle Red Blood Cells
Blood, December 15, 1998; 92(12): 4844 - 4855.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
C. Lytle, T. J. McManus, and M. Haas
A model of Na-K-2Cl cotransport based on ordered ion binding and glide symmetry
Am J Physiol Cell Physiol, February 1, 1998; 274(2): C299 - C309.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
A. Mercado, L. Song, N. Vazquez, D. B. Mount, and G. Gamba
Functional Comparison of the K+-Cl- Cotransporters KCC1 and KCC4
J. Biol. Chem., September 22, 2000; 275(39): 30326 - 30334.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online