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

Details

Serval ID
serval:BIB_65767F8D7940
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Transport of tetraethylammonium by a kidney epithelial cell line (LLC-PK1)
Journal
American Journal of Physiology
Author(s)
Fauth  C., Rossier  B., Roch-Ramel  F.
ISSN
0363-6127
Publication state
Published
Issued date
03/1988
Volume
254
Number
3 Pt 2
Pages
F351-7
Notes
Journal Article
Research Support, Non-U.S. Gov't --- Old month value: Mar
Abstract
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.
Keywords
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
Create date
24/01/2008 14:00
Last modification date
20/08/2019 15:21
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