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. 1973 Aug 1;62(2):147–156. doi: 10.1085/jgp.62.2.147

Dog Red Blood Cells

Adjustment of salt and water content in vitro

John C Parker 1
PMCID: PMC2226112  PMID: 4722565

Abstract

Dog red blood cells (RBC) lack a ouabain-sensitive sodium pump, and yet they are capable of volume regulation in vivo. The present study was designed to find in vitro conditions under which dog RBC could transport sodium outward, against an electrochemical gradient. Cells were first loaded with sodium chloride and water by preincubation in hypertonic saline. They were then incubated at 37°C in media containing physiologic concentrations of sodium, potassium, chloride, bicarbonate, glucose, and calcium. The cells returned to a normal salt and water content in 16–20 h. Without calcium in the medium the cells continued slowly to accumulate sodium. Removal of glucose caused rapid swelling and lysis, whether or not calcium was present. The net efflux of sodium showed a close relationship to medium calcium over a concentration range from 0 to 5 mM. Extrusion of salt and water was also demonstrated in fresh RBC (no hypertonic preincubation) when calcium levels in the media were sufficiently raised. The ion and water movements in these experiments were not influenced by ouabain or by removal of extracellular potassium. Magnesium could not substitute for calcium. It is concluded that dog RBC have an energy-dependent mechanism for extruding sodium chloride which requires external calcium and is quite distinct from the sodium-potassium exchange pump.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. BERNSTEIN R. E. Potassium and sodium balance in mammalian red cells. Science. 1954 Sep 17;120(3116):459–460. doi: 10.1126/science.120.3116.459. [DOI] [PubMed] [Google Scholar]
  2. BOLINGBROKE V., MAIZELS M. Calcium ions and the permeability of human erythrocytes. J Physiol. 1959 Dec;149:563–585. doi: 10.1113/jphysiol.1959.sp006361. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Baker P. F., Blaustein M. P., Hodgkin A. L., Steinhardt R. A. The influence of calcium on sodium efflux in squid axons. J Physiol. 1969 Feb;200(2):431–458. doi: 10.1113/jphysiol.1969.sp008702. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. CHAN P. C., CALABRESE V., THEIL L. S. SPECIES DIFFERENCES IN THE EFFECT OF SODIUM AND POTASSIUM IONS ON THE ATPASE OF ERYTHROCYTE MEMBRANES. Biochim Biophys Acta. 1964 Mar 30;79:424–426. [PubMed] [Google Scholar]
  5. Gary-Bobo C. M., Solomon A. K. Properties of hemoglobin solutions in red cells. J Gen Physiol. 1968 Nov;52(5):825–853. doi: 10.1085/jgp.52.5.825. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Grantham J. J., Kurg M. B., Obloff J. The nature of transtubular Na and K transport in isolated rabbit renal collecting tubules. J Clin Invest. 1970 Oct;49(10):1815–1826. doi: 10.1172/JCI106399. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Hoffman J. F., Kregenow F. M. The characterization of new energy dependent cation transport processes in red blood cells. Ann N Y Acad Sci. 1966 Jul 14;137(2):566–576. doi: 10.1111/j.1749-6632.1966.tb50182.x. [DOI] [PubMed] [Google Scholar]
  8. Hoffman J. F. The red cell membrane and the transport of sodium and potassium. Am J Med. 1966 Nov;41(5):666–680. doi: 10.1016/0002-9343(66)90029-5. [DOI] [PubMed] [Google Scholar]
  9. Lange Y., Lange R. V., Solomon A. K. Cellular inhomogeneity in dog red cells as revealed by sodium flux. J Gen Physiol. 1970 Oct;56(4):438–461. doi: 10.1085/jgp.56.4.438. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Lee P., Miles P. R. Density distribution and cation composition of red blood cells in newborn puppies. J Cell Physiol. 1972 Jun;79(3):377–388. doi: 10.1002/jcp.1040790308. [DOI] [PubMed] [Google Scholar]
  11. Lew V. L. On the ATP dependence of the Ca 2+ -induced increase in K + permeability observed in human red cells. Biochim Biophys Acta. 1971 Jun 1;233(3):827–830. doi: 10.1016/0005-2736(71)90185-4. [DOI] [PubMed] [Google Scholar]
  12. MAIZELS M. Sodium transfer in tortoise erythrocytes. J Physiol. 1956 May 28;132(2):414–441. doi: 10.1113/jphysiol.1956.sp005535. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Miles P. R., Lee P. Sodium and potassium content and membrane transport properties in red blood cells from newborn puppies. J Cell Physiol. 1972 Jun;79(3):367–376. doi: 10.1002/jcp.1040790307. [DOI] [PubMed] [Google Scholar]
  14. Moore E. W. Ionized calcium in normal serum, ultrafiltrates, and whole blood determined by ion-exchange electrodes. J Clin Invest. 1970 Feb;49(2):318–334. doi: 10.1172/JCI106241. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. OMACHI A., MARKEL R. P., HEGARTY H. Ca45 uptake by dog erythrocytes suspended in sodium and potassium chloride solutions. J Cell Comp Physiol. 1961 Apr;57:95–100. doi: 10.1002/jcp.1030570206. [DOI] [PubMed] [Google Scholar]
  16. Parker J. C. Dog red blood cells. Adjustment of density in vivo. J Gen Physiol. 1973 Feb;61(2):146–157. doi: 10.1085/jgp.61.2.146. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Parker J. C. Influence of 2,3-diphosphoglycerate metabolism on sodium-potassium permeability in human red blood cells: studies with bisulfite and other redox agents. J Clin Invest. 1969 Jan;48(1):117–125. doi: 10.1172/JCI105960. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Parker J. C. Ouabain-insensitive effects of metabolism on ion and water content of red blood cells. Am J Physiol. 1971 Jul;221(1):338–342. doi: 10.1152/ajplegacy.1971.221.1.338. [DOI] [PubMed] [Google Scholar]
  19. Parker J. C., Snow R. L. Influence of external ATP on permeability and metabolism of dog red blood cells. Am J Physiol. 1972 Oct;223(4):888–893. doi: 10.1152/ajplegacy.1972.223.4.888. [DOI] [PubMed] [Google Scholar]
  20. Romero P. J., Whittam R. The control by internal calcium of membrane permeability to sodium and potassium. J Physiol. 1971 May;214(3):481–507. doi: 10.1113/jphysiol.1971.sp009445. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Rorive G., Nielsen R., Kleinzeller A. Effect of pH on the water and electrolyte content of renal cells. Biochim Biophys Acta. 1972 May 9;266(2):376–396. doi: 10.1016/0005-2736(72)90095-8. [DOI] [PubMed] [Google Scholar]
  22. Sachs J. R. Ouabain-insensitive sodium movements in the human red blood cell. J Gen Physiol. 1971 Mar;57(3):259–282. doi: 10.1085/jgp.57.3.259. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Schatzmann H. J., Vincenzi F. F. Calcium movements across the membrane of human red cells. J Physiol. 1969 Apr;201(2):369–395. doi: 10.1113/jphysiol.1969.sp008761. [DOI] [PMC free article] [PubMed] [Google Scholar]

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