Time-Dependent Features of Mass Transfer and Transmembrane Potential in Erythrocytes During Equilibration in Cryoprotective Solutions
DOI:
https://doi.org/10.15407/cryo33.02.103Keywords:
physico-mathematical model, mass transfer, erythrocytes, cryoprotectants, transmembrane potentialAbstract
On the basis of the developed physical and mathematical model of mass transfer, which takes into account the transmembrane transfer of non-electrolytes, basic ions and the associated changes in the transmembrane potential, the redistribution of osmotically active substances during equilibration of erythrocytes in cryoprotective solutions was investigated. Time parameters of changes in concentrations of osmotically active substances inside and outside cells, as well as transmembrane electric potential, were calculated. It is shown that during the exposure of human erythrocytes to 1M solutions of glycerol, 1,2-propanediol (1,2-PD) and dimethylsulfoxide (DMSO), the sign of their transmembrane electric potential changes three times, and in solutions of ethylene glycol (EG) and of acetamide (AA) – once. The analysis of the obtained results showed that the most acceptable for further cryopreservation from the point of view of erythrocytes reaching a state close to equilibrium in a 1M solution of glycerol was their equilibration for 5.5 min, and in solutions of DMSO, AA, EG and 1,2-PD with the same concentration – 1 min. At the same time, the cells remain somewhat dehydrated (by 5.5–7.5%), and the concentrations of cryoprotectants inside erythrocytes change insignificantly during longer exposure. The indicated degree of dehydration does not affect cell viability, but reduces the likelihood of intracellular ice formation during subsequent freezing.
Probl Cryobiol Cryomed 2023; 33(2):103–114
References
Benga G. Water transport in red blood cell membranes. Progr Biophys Mol Biol. 1988. 51: 193-245. CrossRef
Best BP. Cryoprotectant toxicity: facts, issues, and questions. Rejuvenation research. 2015; 18(5): 422-42. CrossRef
Brahm J. The permeability of red blood cells to chloride, urea and water. J Exp Biol. 2013; 216(12): 2238-46. CrossRef
Chervy P, Petcut C, Rault D, at al. Organic nanoscrolls from electrostatic interactions between peptides and lipids: assembly steps and structure. Langmuir. 2019; 35: 10648−57. CrossRef
Ciana A, Achilli C, Balduini C, Minetti G. On the association of lipid rafts to the spectrin skeleton in human erythrocytes. Biochim Biophys Acta. 2011; 1808: 183-90. CrossRef
Gordiyenko OI, Gordiyenko YuE, Linnik TP, Gordiyenko EO. Experimental determination of human erythrocyte membrane permeability coefficients for a series of amides. CryoLetters. 2005; 26(1): 65-72. PubMed
Gordiyenko OI, Linnik TP, Gordiyenko EO. Erythrocyte membrane permeability for a series of diols. Bioelectrochemistry. 2004; 62:115-8. CrossRef
Funder J, Wieth JO. Chloride and hydrogen ion distribution between human red cells and plasma. Acta Physiol Scand. 1966; 68: 234-45. CrossRef
Fung YC, Winston CO, Tsang WSO, Pacitucci P. High resolution data on the geometry of red blood cells. Biorheology. 1981;18(2): 369-85. CrossRef
Kahana E, Streichman S, Silver BL. The role of electrostatic forces in the interaction between the membrane and cytoskeleton of human erythrocytes. Biochim Biophys Acta.1991; 1066(1): 1-5. CrossRef
Murray D, Ben-Tal N, Honig B, McLaughlin S. Electrostatic interaction of myristoylated proteins with membranes: simple physics, complicated biology. Structure. 1997; 5(8): 985-9. CrossRef
Samuel E Lux IV. Anatomy of the red cell membrane skeleton: unanswered questions. Blood. 2016; 127(2): 187-99. CrossRef
Sputtek A. Cryopreservation of red blood cells and platelets. Methods Mol Biol. 2007; 368: 283-301. CrossRef
Todrin AF, Timofeyeva OV, Smolyaninova YeI et al. Physicalmathematical model of substance redistribution between the cell and its hypertonic solution environment of penetrating cryoprotectants with relevance to membrane potential. CryoLetters. 2020; 41(4): 209-15. PubMed
Valberg LS, Holt JM, Paulson E, Szivek J. Spectrochemical analysis of sodium, potassium, calcium, magnesium, copper, and zinc in normal human erythrocytes. J Clinic Invest. 1965; 44(3): 379-9. CrossRef
Downloads
Published
How to Cite
Issue
Section
License
This work is licensed under a Creative Commons Attribution 4.0 International License.
Authors who publish with this journal agree to the following terms:
- Authors retain copyright and grant the journal right of first publication with the work simultaneously licensed under a Creative Commons Attribution License that allows others to share the work with an acknowledgement of the work's authorship and initial publication in this journal.
- Authors are able to enter into separate, additional contractual arrangements for the non-exclusive distribution of the journal's published version of the work (e.g., post it to an institutional repository or publish it in a book), with an acknowledgement of its initial publication in this journal.
- Authors are permitted and encouraged to post their work online (e.g., in institutional repositories or on their website) prior to and during the submission process, as it can lead to productive exchanges, as well as earlier and greater citation of published work (See The Effect of Open Access).