» Articles » PMID: 5971026

The Passive Permeability of the Red Blood Cell in Cations

Overview
Journal J Gen Physiol
Specialty Physiology
Date 1966 Sep 1
PMID 5971026
Citations 29
Authors
Affiliations
Soon will be listed here.
Abstract

The efflux of salt from human red blood cells suspended in isotonic sucrose plus low concentrations of salt, was measured under steady-state conditions. The relationship between the efflux and the log of the salt concentration can be fitted by two straight lines with a sharp inflection point, the steeper slope occurring at concentrations below 0.2 mM NaCl. The determining factor in the rate of efflux is the ionic strength rather than the specific monovalent cations or anions and the effects are completely reversible. With an increase in temperature, the effects of reduced ionic strength are more pronounced and the inflection point is shifted toward higher salt concentrations. An increase in pH leads to an increased efflux at a given ionic strength, but the size of the pH effect is small at low ionic strength. At a given pH, the data can be fitted by a simplified form of the Goldman equation suggesting that with reduction in ionic strength, the permeability remains constant until the inflection point is reached. At that ionic strength, a sharp reversible transition to a new permeability state occurs. The permeability increases with an increase in the external but not the internal pH.

Citing Articles

Mathematical Modeling and Optimization of Cryopreservation in Single Cells.

Benson J Methods Mol Biol. 2020; 2180:129-172.

PMID: 32797410 DOI: 10.1007/978-1-0716-0783-1_4.


Continuous removal of glycerol from frozen-thawed red blood cells in a microfluidic membrane device.

Lusianti R, Higgins A Biomicrofluidics. 2014; 8(5):054124.

PMID: 25538811 PMC: 4224679. DOI: 10.1063/1.4900675.


Mathematically optimized cryoprotectant equilibration procedures for cryopreservation of human oocytes.

Davidson A, Benson J, Higgins A Theor Biol Med Model. 2014; 11:13.

PMID: 24649826 PMC: 3994563. DOI: 10.1186/1742-4682-11-13.


Effects of pronase on passive ion permeability of the human red blood cell.

Passow H J Membr Biol. 2013; 6(3):233-58.

PMID: 24177386 DOI: 10.1007/BF01872279.


The cation permeability of erythrocytes in low ionic strength media of various tonicities.

Donlon J, Rothstein A J Membr Biol. 2013; 1(1):37-52.

PMID: 24174041 DOI: 10.1007/BF01869773.


References
1.
Glynn I . Sodium and potassium movements in human red cells. J Physiol. 1956; 134(2):278-310. PMC: 1359203. DOI: 10.1113/jphysiol.1956.sp005643. View

2.
PONDER E, SASLOW G . The measurement of red cell volume: III. Alterations of cell volume in extremely hypotonic solutions. J Physiol. 1931; 73(3):267-96. PMC: 1394352. DOI: 10.1113/jphysiol.1931.sp002810. View

3.
Maizels M . The permeation of erythrocytes by cations. Biochem J. 1935; 29(8):1970-82. PMC: 1266710. DOI: 10.1042/bj0291970. View

4.
Heard D, Seaman G . The influence of pH and ionic strength on the electrokinetic stability of the human erythrocyte membrane. J Gen Physiol. 1960; 43:635-54. PMC: 2195010. DOI: 10.1085/jgp.43.3.635. View

5.
DAVSON H . Studies on the permeability of erythrocytes: The effect of reducing the salt content of the medium surrounding the cell. Biochem J. 1939; 33(3):389-401. PMC: 1264388. DOI: 10.1042/bj0330389. View