THE RELATION BETWEEN PHOSPHATE METABOLISM AND THE TRANSPORT OF CATIONS ACROSS THE CELL MEMBRANE IN THE HUMAN ERYTHROCYTE

1961 ◽  
Vol 39 (12) ◽  
pp. 1879-1894
Author(s):  
Rhoda Blostein ◽  
David Rubinstein ◽  
Orville F. Denstedt

The rate of passage of cations across the red cell membrane, in the direction of the respective ionic gradients, in blood preserved with glucose at 4 °C, is not diminished upon the addition of inosine, notwithstanding the induced formation of substantial amounts of phosphate esters, including ATP, in the cells. The movement of cations, however, is retarded on the addition of glucose or inorganic phosphate, and on increase in the concentration of hydrogen ions. It would appear, therefore, that the movement of cations across the membrane, at 4 °C, is influenced little, if at all, by the metabolic activity of the cell.When the temperature of the preserved blood is returned to 37° the rate of movement of cations across the cell membrane against their respective gradients is greatest in cells which had either been preserved or have been incubated with inosine even if the remainder of the inosine has been removed. Inosine is more effective than glucose in bringing about the restoration of cation composition in preserved red cells at 37°. The degree of restoration is greater in the presence of glucose than in its absence. Arsenate inhibits the transport of cations against the gradients. Evidence is given that the capacity of the cells to restore the cation distribution at 37 °C is determined largely by the concentration of the phosphate ester intermediates.

Cryobiology ◽  
1986 ◽  
Vol 23 (2) ◽  
pp. 134-140 ◽  
Author(s):  
A. Rubinacci ◽  
B. Fuller ◽  
F. Wuytack ◽  
W. De Loecker

1964 ◽  
Vol 4 (2) ◽  
pp. 115-135 ◽  
Author(s):  
R.P. Rand ◽  
A.C. Burton

1974 ◽  
Vol 64 (6) ◽  
pp. 706-729 ◽  
Author(s):  
W. R. Redwood ◽  
E. Rall ◽  
W. Perl

The permeability coefficients of dog red cell membrane to tritiated water and to a series of[14C]amides have been deduced from bulk diffusion measurements through a "tissue" composed of packed red cells. Red cells were packed by centrifugation inside polyethylene tubing. The red cell column was pulsed at one end with radiolabeled solute and diffusion was allowed to proceed for several hours. The distribution of radioactivity along the red cell column was measured by sequential slicing and counting, and the diffusion coefficient was determined by a simple plotting technique, assuming a one-dimensional diffusional model. In order to derive the red cell membrane permeability coefficient from the bulk diffusion coefficient, the red cells were assumed to be packed in a regular manner approximating closely spaced parallelopipeds. The local steady-state diffusional flux was idealized as a one-dimensional intracellular pathway in parallel with a one-dimensional extracellular pathway with solute exchange occurring within the series pathway and between the pathways. The diffusion coefficients in the intracellular and extracellular pathways were estimated from bulk diffusion measurements through concentrated hemoglobin solutions and plasma, respectively; while the volume of the extracellular pathway was determined using radiolabeled sucrose. The membrane permeability coefficients were in satisfactory agreement with the data of Sha'afi, R. I., C. M. Gary-Bobo, and A. K. Solomon (1971. J. Gen. Physiol. 58:238) obtained by a rapid-reaction technique. The method is simple and particularly well suited for rapidly permeating solutes.


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