Transport of tetraethylammonium by a kidney epithelial cell line (LLC-PK1)

Détails

ID Serval
serval:BIB_65767F8D7940
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Transport of tetraethylammonium by a kidney epithelial cell line (LLC-PK1)
Périodique
American Journal of Physiology
Auteur⸱e⸱s
Fauth  C., Rossier  B., Roch-Ramel  F.
ISSN
0363-6127
Statut éditorial
Publié
Date de publication
03/1988
Volume
254
Numéro
3 Pt 2
Pages
F351-7
Notes
Journal Article
Research Support, Non-U.S. Gov't --- Old month value: Mar
Résumé
We investigated whether the LLC-PK1 epithelial cell line (which shows many characteristics of proximal tubular cells) also is capable of transporting an organic ion. Suspended LLC-PK1 cells accumulated tetraethylammonium (TEA). The uptake showed characteristics of a facilitated mechanism; TEA uptake was saturable and temperature-dependent and was inhibited by other organic cations. Quinine and mepiperphenidol were the most potent inhibitors, whereas N1-methylnicotinamide and morphine inhibited the transport system only slightly at doses of 10(-3) M. Basolateral-to-apical TEA flux through LLC-PK1 monolayers was five to six times larger than that of mannitol, a nontransported compound, whereas apical-to-basolateral TEA and mannitol fluxes were equal. Only the basolateral-to-apical TEA flux was inhibited by quinine. Under similar experimental conditions, no transport of p-aminohippuric acid was observed. It is concluded that LLC-PK1 cells are able to transport TEA, as do cells of the proximal tubule.
Mots-clé
Animals Biological Transport Cations/pharmacology Cell Line Culture Media Cytological Techniques Epithelial Cells Epithelium/metabolism Kidney/cytology/*metabolism Osmolar Concentration Ouabain/pharmacology Temperature Tetraethylammonium Tetraethylammonium Compounds/antagonists & inhibitors/*pharmacokinetics Time Factors
Pubmed
Web of science
Création de la notice
24/01/2008 14:00
Dernière modification de la notice
20/08/2019 15:21
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