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
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.
Références
J Physiol. 1977 Apr;266(3):727-49
pubmed: 17003
J Gen Physiol. 1991 Feb;97(2):321-49
pubmed: 1849960
J Gen Physiol. 1982 May;79(5):791-819
pubmed: 7097244
J Am Soc Nephrol. 1992 Jun;2(12):1689-96
pubmed: 1498276
Biochem Cell Biol. 2011 Apr;89(2):200-15
pubmed: 21455271
J Physiol. 1972 Aug;224(3):583-610
pubmed: 5071931
J Physiol. 1983 Jun;339:339-54
pubmed: 6887027
Am J Physiol. 1991 Apr;260(4 Pt 1):C778-83
pubmed: 1902060
J Gen Physiol. 2023 Aug 7;155(8):
pubmed: 37389569
Blood. 1980 Dec;56(6):969-77
pubmed: 6777001
Methods Enzymol. 1989;173:160-75
pubmed: 2674610
J Gen Physiol. 1983 Feb;81(2):283-304
pubmed: 6842175
J Proteome Res. 2017 Aug 4;16(8):2752-2761
pubmed: 28689405
Biochim Biophys Acta. 1987 Jun 30;900(2):282-90
pubmed: 3297147
Pflugers Arch. 2019 Dec;471(11-12):1359-1368
pubmed: 31734718
J Exp Biol. 2013 Jun 15;216(Pt 12):2238-46
pubmed: 23470663
J Gen Physiol. 1983 Jul;82(1):1-23
pubmed: 6411854
J Biol Chem. 2002 Sep 13;277(37):34101-8
pubmed: 12093813
J Gen Physiol. 1977 Sep;70(3):283-306
pubmed: 19556
Blood Transfus. 2012 May;10 Suppl 2:s46-54
pubmed: 22890268
J Membr Biol. 1993 Apr;133(1):85-97
pubmed: 8391582
J Biol Chem. 2002 Sep 27;277(39):36782-6
pubmed: 12133842
Front Physiol. 2012 Jun 26;3:217
pubmed: 22745630
J Gen Physiol. 1973 Feb;61(2):185-206
pubmed: 4688320
J Gen Physiol. 2023 Oct 2;155(10):
pubmed: 37535830