» Articles » PMID: 9138568

Membrane Potential and Human Erythrocyte Shape

Overview
Journal Biophys J
Publisher Cell Press
Specialty Biophysics
Date 1997 Mar 1
PMID 9138568
Citations 10
Authors
Affiliations
Soon will be listed here.
Abstract

Altered external pH transforms human erythrocytes from discocytes to stomatocytes (low pH) or echinocytes (high pH). The process is fast and reversible at room temperature, so it seems to involve shifts in weak inter- or intramolecular bonds. This shape change has been reported to depend on changes in membrane potential, but control experiments excluding roles for other simultaneously varying cell properties (cell pH, cell water, and cell chloride concentration) were not reported. The present study examined the effect of independent variation of membrane potential on red cell shape. Red cells were equilibrated in a set of solutions with graduated chloride concentrations, producing in them a wide range of membrane potentials at normal cell pH and cell water. By using assays that were rapid and accurate, cell pH, cell water, cell chloride, and membrane potential were measured in each sample. Cells remained discoid over the entire range of membrane potentials examined (-45 to +45 mV). It was concluded that membrane potential has no independent effect on red cell shape and does not mediate the membrane curvature changes known to occur in red cells equilibrated at altered pH.

Citing Articles

Insights on the Mechanisms of the Protective Action of Naringenin, Naringin and Naringin Dihydrochalcone on Blood Cells in Terms of Their Potential Anti-Atherosclerotic Activity.

Kazmierczak T, Cyboran-Mikolajczyk S, Trochanowska-Pauk N, Walski T, Nowicka P, Bonarska-Kujawa D Molecules. 2025; 30(3).

PMID: 39942651 PMC: 11820682. DOI: 10.3390/molecules30030547.


Protective Effect of Polyphenolic Extracts from L. and on Erythrocyte Membrane.

Kazmierczak T, Meczarska K, Lachowicz-Wisniewska S, Cyboran-Mikolajczyk S, Oszmianski J, Bonarska-Kujawa D Molecules. 2024; 29(13).

PMID: 38999046 PMC: 11243633. DOI: 10.3390/molecules29133090.


Bioelectricity in dental medicine: a narrative review.

Min Q, Gao Y, Wang Y Biomed Eng Online. 2024; 23(1):3.

PMID: 38172866 PMC: 10765628. DOI: 10.1186/s12938-023-01189-6.


Influence of Na+ disorder on cytoplasmic conductivity and cellular electromagnetic (EM) energy absorption of human erythrocytes (PONE-D-21-36089).

Sudsiri C, Ritchie R PLoS One. 2023; 18(2):e0277044.

PMID: 36821542 PMC: 9949639. DOI: 10.1371/journal.pone.0277044.


Hemolysis Pathways during Storage of Erythrocytes and Inter-Donor Variability in Erythrocyte Morphology.

Melzak K, Spouge J, Boecker C, Kirschhofer F, Brenner-Weiss G, Bieback K Transfus Med Hemother. 2021; 48(1):39-47.

PMID: 33708051 PMC: 7923927. DOI: 10.1159/000508711.


References
1.
Freedman J, Hoffman J . Ionic and osmotic equilibria of human red blood cells treated with nystatin. J Gen Physiol. 1979; 74(2):157-85. PMC: 2228501. DOI: 10.1085/jgp.74.2.157. View

2.
TROTTER W . The slide-coverslip disc-sphere transformation in mammalian erythrocytes. Br J Haematol. 1956; 2(1):65-74. DOI: 10.1111/j.1365-2141.1956.tb06685.x. View

3.
Schindler M, Koppel D, Sheetz M . Modulation of membrane protein lateral mobility by polyphosphates and polyamines. Proc Natl Acad Sci U S A. 1980; 77(3):1457-61. PMC: 348514. DOI: 10.1073/pnas.77.3.1457. View

4.
Lovrien R, Anderson R . Stoichiometry of wheat germ agglutinin as a morphology controlling agent and as a morphology controlling agent and as a morphology protective agent for the human erythrocyte. J Cell Biol. 1980; 85(3):534-48. PMC: 2111459. DOI: 10.1083/jcb.85.3.534. View

5.
Sheetz M, Casaly J . 2,3-Diphosphoglycerate and ATP dissociate erythrocyte membrane skeletons. J Biol Chem. 1980; 255(20):9955-60. View