Urea transport in human red blood cells: Donor variation compared to chloride, glucose, and water transport

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Urea transport in human red blood cells : Donor variation compared to chloride, glucose, and water transport. / Leifelt, Jonas; Dziegiel, Morten Hanefeld; Brahm, Jesper.

I: The Journal of general physiology, Bind 155, Nr. 10, e202213321, 2023.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Leifelt, J, Dziegiel, MH & Brahm, J 2023, 'Urea transport in human red blood cells: Donor variation compared to chloride, glucose, and water transport', The Journal of general physiology, bind 155, nr. 10, e202213321. https://doi.org/10.1085/jgp.202213321

APA

Leifelt, J., Dziegiel, M. H., & Brahm, J. (2023). Urea transport in human red blood cells: Donor variation compared to chloride, glucose, and water transport. The Journal of general physiology, 155(10), [e202213321]. https://doi.org/10.1085/jgp.202213321

Vancouver

Leifelt J, Dziegiel MH, Brahm J. Urea transport in human red blood cells: Donor variation compared to chloride, glucose, and water transport. The Journal of general physiology. 2023;155(10). e202213321. https://doi.org/10.1085/jgp.202213321

Author

Leifelt, Jonas ; Dziegiel, Morten Hanefeld ; Brahm, Jesper. / Urea transport in human red blood cells : Donor variation compared to chloride, glucose, and water transport. I: The Journal of general physiology. 2023 ; Bind 155, Nr. 10.

Bibtex

@article{3454c64a2ae346d3babbe3e2690bd3b1,
title = "Urea transport in human red blood cells: Donor variation compared to chloride, glucose, and water transport",
abstract = "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.",
author = "Jonas Leifelt and Dziegiel, {Morten Hanefeld} and Jesper Brahm",
note = "Publisher Copyright: {\textcopyright} 2023 Leifelt et al.",
year = "2023",
doi = "10.1085/jgp.202213321",
language = "English",
volume = "155",
journal = "Journal of General Physiology",
issn = "0022-1295",
publisher = "Rockefeller University Press",
number = "10",

}

RIS

TY - JOUR

T1 - Urea transport in human red blood cells

T2 - Donor variation compared to chloride, glucose, and water transport

AU - Leifelt, Jonas

AU - Dziegiel, Morten Hanefeld

AU - Brahm, Jesper

N1 - Publisher Copyright: © 2023 Leifelt et al.

PY - 2023

Y1 - 2023

N2 - 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.

AB - 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.

U2 - 10.1085/jgp.202213321

DO - 10.1085/jgp.202213321

M3 - Journal article

C2 - 37535830

AN - SCOPUS:85166548405

VL - 155

JO - Journal of General Physiology

JF - Journal of General Physiology

SN - 0022-1295

IS - 10

M1 - e202213321

ER -

ID: 362331348