CL- AND K+ TRANSPORT IN HUMAN BILIARY CELL-LINES
CL- AND K+ TRANSPORT IN HUMAN BILIARY CELL-LINES
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DOI:
10.1016/0016-5085(93)90661-u
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发表时间:
1993-06-01
期刊:
影响因子:
29.4
通讯作者:
FITZ, JG
中科院分区:
文献类型:
--
作者:
BASAVAPPA, S;MIDDLETON, J;FITZ, JG
Background:The cellular mechanisms which contribute to billing secretion and absorption are not fully defined. The purpose of these studies was to evaluate the membrane ion transport properties of Mz-ChA-1 and Sk-ChA-1 cell lines derived from human biliary tumors.Methods:In cultured cells,125I and36Cl efflux rates were used to assess membrane anion permeability, and86Rb efflux rates were used to assess K+permeability.Results:Sections of tumors grown on BALB/ Urd mice were used for morphological evaluation and for detection of cystic fibrosis transmembrane conductance regulator (CFTR), the protein product of the cystic fibrosis gene. There was organized development of ductular structures and cells stained for γ-glutamyl transpeptidase and CK-19. Immunoperoxidase staining for CFTR, which is likely a Cl−channel, was also present. Increases in intracellular Ca2+stimulated by exposure to ionomycin or thapsigargin increased efflux of125I,36Cl, and86Rb. Efflux of125I was greater than36Cl, and anion efflux was inhibited by the Cl−channel blocker 4,4′-diisothiocyanatostilbene-2,2′-disulfonic acid. Increases in 5′-cyclic adenosine monophosphate increased efflux of36Cl greater than125I but had no effect on86Rb efflux. Both cell lines possess bumetanide-sensitive86Rb uptake consistent with possible Na+/K+/2Cl−cotransport.Conclusions:These human cell lines retain certain phenotypic features of differentiated biliary cells and may be useful for further investigation of biliary fluid and electrolyte transport.