The hemoglobin concentration in the sickle erythrocyte is a major determinant of cytoplasmic viscosity and greatly influences the rate and which hemoglobin S polymerizes following deoxygenation. This observation has created much interest in cell volume regulation in the sickle erythrocyte. The identification of factors which cause cell dehydration improves our understanding of the pathogenesis of sickling. The ability to dilute the hemoglobin content of the sickle erythrocyte, which inhibits gelation of hemoglobin S, offers a new therapeutic approach to the treatment of sickle cell disease. The proposed work will focus on several relationships between membrane transport, cell volume regulation, and sickling. It is agreed that during reversible sickling, large """"""""downhill"""""""" fluxes of Na, K, and calcium occur. The possibility that these fluxes of ions are involved in cellular dehydration or are the signal for dehydration will be extensively investigated in terms of recent information about passive ion transport in mammalian red cells. A method of deoxygenation has been devised in which ion and water movements which occur with deoxygenation can be studied under controlled conditions. The information gained may lead to an improved understanding of the pathgenesis of sickling. This in turn may produce practical methods, using principles of cell volume regulation, which will inhibit hemoglobin S gelation.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Unknown (R23)
Project #
5R23HL030467-02
Application #
3448513
Study Section
Hematology Subcommittee 2 (HEM)
Project Start
1984-06-01
Project End
1987-05-31
Budget Start
1985-06-01
Budget End
1986-05-31
Support Year
2
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Type
Schools of Medicine
DUNS #
078861598
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
Berkowitz, L R (1990) Loop diuretic and anion modification of NEM-induced K transport in human red blood cells. Am J Physiol 258:C622-9
Berkowitz, L R; Orringer, E P (1987) Cell volume regulation in hemoglobin CC and AA erythrocytes. Am J Physiol 252:C300-6
Murphy, E; Berkowitz, L R; Orringer, E et al. (1987) Cytosolic free calcium levels in sickle red blood cells. Blood 69:1469-74
Berkowitz, L R; Walstad, D; Orringer, E P (1987) Effect of N-ethylmaleimide on K transport in density-separated human red blood cells. Am J Physiol 253:C7-12
Murphy, E; Levy, L; Berkowitz, L R et al. (1986) Nuclear magnetic resonance measurement of cytosolic free calcium levels in human red blood cells. Am J Physiol 251:C496-504
Berkowitz, L R; Orringer, E P (1985) Passive sodium and potassium movements in sickle erythrocytes. Am J Physiol 249:C208-14