Adenosine triphosphate activates ion permeabilities in biliary epithelial cells.
Adenosine triphosphate activates ion permeabilities in biliary epithelial cells.
复制标题
三磷酸腺苷激活胆管上皮细胞的离子渗透性。
DOI:
10.1016/0016-5085(94)90082-5
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发表时间:
1994
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:
McGill,JM;Basavappa,S;Mangel,AW;Shimokura,GH;Middleton,JP;Fitz,JG
Background/Aims:The biliary epithelium contributes to bile formation through absorption and secretion of fluid and electrolytes. The effects of extracellular nucleotides on membrane ion transport were assessed in isolated bile duct cells from rats and Mz-ChA-1 cells from a human cholangiocarcinoma.Methods:The rates of efflux of125I and86Rb were used to assess membrane CI−and K+permeabilities, respectively. Patch clamp recordings of whole cell currents were used to evaluate the properties of adenosine triphosphate (ATP)-activated currents.Results:Purinergic receptor agonists ATP and uridine triphosphate stimulated125I and86Rb efflux about twofold above basal levels. The effects were reproduced by a nonhydrolyzable analogue of ATP (adenosine 5′-O-[3-thiophosphate]) and were unaffected by an adenosine receptor blocker xanthine amine congener.125I efflux was also stimulated by adenosine and its receptor agonists 5′-N-ethylcar-boxamidoadenosine,N6-(2-phenylisopropyl)adenosine; these effects were inhibited by xanthine amine congener, suggesting a separate adenosine receptor. ATP, adenosine 5′-O-(3-thiophosphate), and uridine triphosphate each stimulated release of Ca2+from intracellular stores, whereas adenosine had no effect. In whole cell recordings of Mz-ChA-1 cells, ATP activated an early transient outward current consistent with a K+conductance and a later, sustained inward current consistent with a CI−conductance.Conclusions:Biliary cells possess at least two classes of nucleotide receptors that modulate membrane ion permeability through Ca2+-dependent and -independent pathways, and ATP may be involved in the regulation of biliary secretion.
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影响因子:
3.7
作者:
Boynton,AL;Cooney,RV;Hill,TD;Nilsson,T;Arkhammar,P;Berggren,PO
通讯作者:
Berggren,PO
影响因子:
29.4
作者:
BASAVAPPA, S;MIDDLETON, J;FITZ, JG
通讯作者:
FITZ, JG
影响因子:
5.2
作者:
G. Burnstock
通讯作者:
G. Burnstock
DOI:
--
发表时间:
1992
期刊:
The Journal of biological chemistry
影响因子:
--
作者:
Kato,A;Gores,GJ;LaRusso,NF
通讯作者:
LaRusso,NF
DOI:
10.1152/ajpgi.1992.263.1.g69
发表时间:
1992
期刊:
The American journal of physiology
影响因子:
--
作者:
Igimi,H;Yamamoto,F;Lee,SP
通讯作者:
Lee,SP