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


Journal

The Journal of general physiology
ISSN: 1540-7748
Titre abrégé: J Gen Physiol
Pays: United States
ID NLM: 2985110R

Informations de publication

Date de publication:
02 10 2023
Historique:
received: 21 12 2022
revised: 12 05 2023
revised: 18 06 2023
accepted: 12 07 2023
pmc-release: 02 02 2024
medline: 7 8 2023
pubmed: 3 8 2023
entrez: 3 8 2023
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 37535830
pii: 276146
doi: 10.1085/jgp.202213321
pmc: PMC10397051
pii:
doi:

Substances chimiques

Chlorides 0
Glucose IY9XDZ35W2

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2023 Leifelt et al.

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Auteurs

Jonas Leifelt (J)

Department of Cellular and Molecular Medicine, The Faculty of Health, University of Copenhagen, Copenhagen, Denmark.

Morten Hanefeld Dziegiel (MH)

Department of Clinical Medicine, Copenhagen University of Copenhagen, Copenhagen, Denmark.
Department of Clinical Immunology, Copenhagen University Hospital (Rigshospitalet), Copenhagen, Denmark.

Jesper Brahm (J)

Department of Cellular and Molecular Medicine, The Faculty of Health, University of Copenhagen, Copenhagen, Denmark.

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Classifications MeSH