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pubmed:abstractText |
The mechanism(s) of [35S]sulphate transport was investigated in basolateral liver plasma-membrane vesicles of the little skate elasmobranch, Raja erinacea. Imposition of an intravesicular alkaline pH gradient (pH 8.0 in/pH 6.0 out) stimulated sulphate uptake 5-10-fold compared with pH-equilibrated (pH 8.0 in = out) conditions and 2-3-fold over equilibrium sulphate uptake (overshoot). This pH-gradient-stimulated sulphate uptake was temperature-dependent, saturable with increasing concentrations of sulphate and could be inhibited by the protonophore carbonyl cyanide m-chlorophenylhydrazone and the anion-transport inhibitors 4,4'-di-isothiocyanostilbene-2,2'-disulphonic acid (DIDS) and probenecid, cis-Inhibition of pH-gradient-driven sulphate uptake was observed with sulphate, oxalate, cholate and bromosulphophthalein, but not with chloride and taurocholate. In addition, sulphate and oxalate trans-stimulated [35S]sulphate uptake under pH-equilibrated conditions. Although also stimulated by an inside-alkaline pH gradient, transmembrane transport of [3H]cholate was not inhibited by DIDS, suggesting that its pH-gradient-driven uptake is not mediated by an anion-transport 'carrier'. In conclusion, these studies indicate that a basolateral plasma-membrane sulphate-transport system has evolved in skate hepatocytes and is similar to that in mammalian liver cells. This archaic anion-exchange system co-transports certain organic anions such as oxalate and has developed early in vertebrate evolution.
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pubmed:publicationType |
Journal Article,
In Vitro,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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