We determined the permeability (P, cm/s) of unmodified human red blood cells (HRBC) to urea (Pu), chloride (PCl), glucose (Pglu), and water diffusion (Pd) under conditions of self-exchange (SE) with the continuous flow tube method at pH 7.2, 25°C. Among 24 donors, Pu at 1 mM varied >100%. Two of the donors were also tested in 1983. Their Pu had decreased by 77 and 90%. High age in males and Kidd genotype Jk(a+,b+), but not blood types AB0, appear related to low Pu. For one of the two donors, PCl (150 mM, 38°C, pH 7.2), Pglu (1 mM, 38°C, pH 7.2), and Pd (55.5 M, 25°C, pH 7.2) were determined then and now and showed no significant changes with age. The results from six more donors show donor PCl, Pglu, and Pd in the range of ≈1%. PCl and Pglu are vital for the metabolism of cells and tissues, and we see but little donor variation, and so far, no phenotypes without glucose (GLUT1) and anion (AE1) transporters in HRBC. Phenotypes with no urea transporter (UT-B) or no water transporters (aquaporin, AQP1) are registered and are compatible with life. Our results are in line with the concept that the solutes do not share pathways in common. The great donor variation in Pu must be considered in comparative transport physiological studies.
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August 02 2023
Urea transport in human red blood cells: Donor variation compared to chloride, glucose, and water transport
Jonas Leifelt
,
Jonas Leifelt
(Data curation, Formal analysis, Investigation, Methodology)
1Department of Cellular and Molecular Medicine, The Faculty of Health,
University of Copenhagen
, Copenhagen, Denmark
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Morten Hanefeld Dziegiel
,
Morten Hanefeld Dziegiel
(Resources, Writing - review & editing)
2Department of Clinical Medicine,
Copenhagen University of Copenhagen
, Copenhagen, Denmark
3Department of Clinical Immunology,
Copenhagen University Hospital (Rigshospitalet)
, Copenhagen, Denmark
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Jesper Brahm
(Conceptualization, Data curation, Formal analysis, Investigation, Methodology, Project administration, Resources, Software, Supervision, Validation, Visualization, Writing - original draft, Writing - review & editing)
1Department of Cellular and Molecular Medicine, The Faculty of Health,
University of Copenhagen
, Copenhagen, Denmark
Correspondence to Jesper Brahm: jbrahm@sund.ku.dk
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Jonas Leifelt
Data curation, Formal analysis, Investigation, Methodology
1Department of Cellular and Molecular Medicine, The Faculty of Health,
University of Copenhagen
, Copenhagen, Denmark
Morten Hanefeld Dziegiel
Resources, Writing - review & editing
2Department of Clinical Medicine,
Copenhagen University of Copenhagen
, Copenhagen, Denmark
3Department of Clinical Immunology,
Copenhagen University Hospital (Rigshospitalet)
, Copenhagen, Denmark
Jesper Brahm
Conceptualization, Data curation, Formal analysis, Investigation, Methodology, Project administration, Resources, Software, Supervision, Validation, Visualization, Writing - original draft, Writing - review & editing
1Department of Cellular and Molecular Medicine, The Faculty of Health,
University of Copenhagen
, Copenhagen, Denmark
Correspondence to Jesper Brahm: jbrahm@sund.ku.dk
Disclosures: The authors declare no competing interests exist.
Received:
December 21 2022
Revision Received:
May 12 2023
Revision Received:
June 18 2023
Accepted:
July 12 2023
Online ISSN: 1540-7748
Print ISSN: 0022-1295
© 2023 Leifelt et al.
2023
Leifelt et al.
This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).
J Gen Physiol (2023) 155 (10): e202213321.
Article history
Received:
December 21 2022
Revision Received:
May 12 2023
Revision Received:
June 18 2023
Accepted:
July 12 2023
Citation
Jonas Leifelt, Morten Hanefeld Dziegiel, Jesper Brahm; Urea transport in human red blood cells: Donor variation compared to chloride, glucose, and water transport. J Gen Physiol 2 October 2023; 155 (10): e202213321. doi: https://doi.org/10.1085/jgp.202213321
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