Phosphoinositides present in the erythrocyte membrane have a unique function when compared to many other cell types. In the erythrocyte the phosphoinositides play a structural role in contrast to the more commonly observed signal transduction function. Specifically, these lipids have been implicated in the control of the native biconcave shape of the erythrocyte as well as serving as a component in the skeletal complex between band 4.1 and glycophorin. With this background, the focus of the present proposal is to understand the physiological function and enzymology of the phosphoinositides in erythrocytes. The first goal is to purify and characterize phosphatidylinositol 4-phosphate kinase. This enzyme, which has been shown to be a component of the erythrocyte skeleton, is a critical element in controlling the level of phosphatidylinositol 4,5-bisphosphate in the membrane. Therefore, the enzyme will be purified, its kinetic properties examined both on and off the skeleton, and the binding site for this enzyme on the skeleton will be identified. The second goal of this proposal is to examine the phosphoinositide metabolism of senescent erythrocytes. Mature erythrocytes cannot synthesize additional phosphatidylinositol so that the possibility that they have a decreasing level of this lipid during their life span is of particular interest with regards to the viability of aged erythrocytes. A recently developed procedure for the isolation of senescent erythrocytes will be utilized; this procedure involves the biotinylation of rabbit erythrocytes. The reinfusion of the derivatized cells and their eventual recovery, after in vivo aging, by attachment to an avidin support. The third goal of the project is to examine the maintenance of distinct pools of phosphoinositides within the erythrocyte membrane. Preliminary work has shown that a sizable portion of the erythrocyte phosphoinositides are associated with the skeleton and that the exchange between this pool and the bulk of the phosphoinositides is slow enough to be readily studied. The final goal of the project is to examine patients with undefined hemolytic anemia for the presence of abnormalities in the phosphoinositide pathways.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
2R01DK035220-04
Application #
3233500
Study Section
Biochemistry Study Section (BIO)
Project Start
1985-09-23
Project End
1993-08-31
Budget Start
1988-09-01
Budget End
1989-08-31
Support Year
4
Fiscal Year
1988
Total Cost
Indirect Cost
Name
Scripps Research Institute
Department
Type
DUNS #
City
San Diego
State
CA
Country
United States
Zip Code
92037
Heilmann, E; Hynes, L A; Friese, P et al. (1994) Dog platelets accumulate intracellular fibrinogen as they age. J Cell Physiol 161:23-30
Peng, J; Friese, P; George, J N et al. (1994) Alteration of platelet function in dogs mediated by interleukin-6. Blood 83:398-403
Peng, J; Friese, P; Heilmann, E et al. (1994) Aged platelets have an impaired response to thrombin as quantitated by P-selectin expression. Blood 83:161-6
Dale, G L; Gaddy, P; Pikul, F J (1994) Antibodies against biotinylated proteins are present in normal human serum. J Lab Clin Med 123:365-71
Heilmann, E; Friese, P; Anderson, S et al. (1993) Biotinylated platelets: a new approach to the measurement of platelet life span. Br J Haematol 85:729-35
Dale, G L; Norenberg, S L; Suzuki, T et al. (1989) Altered adenine nucleotide metabolism in senescent erythrocytes from the rabbit. Prog Clin Biol Res 319:259-69;discussion 270-3
Dale, G L (1989) Radioisotopic assay for erythrocyte adenosine 5'-monophosphate deaminase. Clin Chim Acta 182:1-7
Suzuki, T; Dale, G L (1989) Membrane proteins in senescent erythrocytes. Biochem J 257:37-41
Dale, G L; Suzuki, T (1988) Erythrocytes attached to a wheat germ agglutinin coated surface display an altered phospholipid metabolism. J Cell Biochem 38:1-11
Dale, G L (1988) Use of the dye Janus green to facilitate quantitative analysis of phosphoinositides. J Chromatogr 424:445-8

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