Rheologic properties of senescent erythrocytes: loss of surface area and volume with red blood cell age.

The rheologic properties of senescent erythrocytes have been examined using two models of red blood cell (RBC) aging. In the rabbit, aged erythrocytes were isolated after biotinylation, in vivo aging, and subsequent recovery on an avidin support. Aged RBCs from the mouse were obtained using the Ganzoni hypertransfusion model that suppresses erythropoiesis for prolonged periods of time allowing preexisting cells to age in vivo. In both cases, the aged erythrocytes were found by ektacytometry to have decreased deformability due to diminished surface area and cellular dehydration. The aged rabbit erythrocytes were further characterized by micropipette methods that documented an average surface area decrease of 10.5% and a volume decrease of 8.4% for the cells that were 50 days old. Because both the surface area and volume decreased with cell age, there was little change in surface-to-volume ratio (sphericity) during aging. The aged cells were found to have normal membrane elasticity. In addition, human RBCs were fractionated over Stractan density gradients and the most dense cells were found to have rheologic properties similar to those reported for the aged RBCs from rabbits and mice, although the absolute magnitude of the changes in surface area and volume were considerably greater for the human cells. Thus, stringent density fractionation protocols that result in isolation of the most dense 1% of cells can produce a population of human cells with rheologic properties similar to senescent cells obtained in other species. The data indicate that progressive loss of cell area and cell dehydration are characteristic features of cell aging.

[1]  T. Suzuki,et al.  Biotinylated erythrocytes: in vivo survival and in vitro recovery , 1987 .

[2]  J. Friedman,et al.  Studies of density fractions of normal human erythrocytes labeled with iron-59 in vivo. , 1979, The Journal of laboratory and clinical medicine.

[3]  R. Hillman,et al.  Red cell aging in vivo. , 1971, The Journal of clinical investigation.

[4]  R M Hochmuth,et al.  Measurement of the elastic modulus for red cell membrane using a fluid mechanical technique. , 1973, Biophysical journal.

[5]  P. Low,et al.  The role of hemoglobin denaturation and band 3 clustering in red blood cell aging. , 1985, Science.

[6]  T. Mueller,et al.  Does cell density correlate with red cell age? , 1983, Biomedica biochimica acta.

[7]  G. Dale,et al.  Time-dependent loss of adenosine 5'-monophosphate deaminase activity may explain elevated adenosine 5'-triphosphate levels in senescent erythrocytes. , 1989, Blood.

[8]  A Leung,et al.  Static and dynamic rigidities of normal and sickle erythrocytes. Major influence of cell hemoglobin concentration. , 1984, The Journal of clinical investigation.

[9]  E. Beutler,et al.  Age-Related Red Cell Enzymes in Children with Transient Erythroblastopenia of Childhood and with Hemolytic Anemia , 1985, Pediatric Research.

[10]  P. Agre,et al.  Inheritance pattern and clinical response to splenectomy as a reflection of erythrocyte spectrin deficiency in hereditary spherocytosis. , 1986, The New England journal of medicine.

[11]  G. Nash,et al.  Erythrocyte membrane elasticity during in vivo ageing. , 1981, Biochimica et Biophysica Acta.

[12]  R. Waugh,et al.  Reductions of erythrocyte membrane viscoelastic coefficients reflect spectrin deficiencies in hereditary spherocytosis. , 1988, The Journal of clinical investigation.

[13]  H. Lutz,et al.  Naturally occurring anti-band 3 antibodies and complement in phagocytosis of oxidatively-stressed and in clearance of senescent red cells. , 1988, Blood cells.

[14]  N. Mohandas,et al.  Osmotic gradient ektacytometry: comprehensive characterization of red cell volume and surface maintenance. , 1983, Blood.

[15]  T. Suzuki,et al.  Senescent erythrocytes: isolation of in vivo aged cells and their biochemical characteristics. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[16]  R. A. Cooper Loss of membrane components in the pathogenesis of antibody-induced spherocytosis. , 1972, The Journal of clinical investigation.

[17]  A. Allison,et al.  Turnovers of Erythrocytes and Plasma Proteins in Mammals , 1960, Nature.

[18]  N. Mohandas,et al.  Analysis of factors regulating erythrocyte deformability. , 1980, The Journal of clinical investigation.

[19]  E. Evans,et al.  Structure and deformation properties of red blood cells: concepts and quantitative methods. , 1989, Methods in enzymology.

[20]  M. R. Clark,et al.  Senescence of red blood cells: progress and problems. , 1988, Physiological reviews.

[21]  W. Groner,et al.  Automated quantitation of cell density distribution and hyperdense cell fraction in RBC disorders. , 1989, Blood.

[22]  P. Agre,et al.  Decreased membrane mechanical stability and in vivo loss of surface area reflect spectrin deficiencies in hereditary spherocytosis. , 1988, The Journal of clinical investigation.

[23]  J. de Regt,et al.  51Cr-half life time of heavy and light human erythrocytes. , 1970, Scandinavian journal of haematology.

[24]  W. Groner,et al.  Cell Membrane and Volume Changes during Red Cell Development and Aging a , 1989, Annals of the New York Academy of Sciences.