1. Identification and Functional Characterization of Bilitranslocase in Sea-Bass ( Dicentrarchus labrax ) Hepatopancreas.
- Author
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Delneri, A., Franca, R., Terdoslavich, M., Montanič, S., Šerbec, V.Čurin, Tramer, F., Francese, M., and Passamonti, S.
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EUROPEAN seabass ,BILIRUBIN ,VASCULAR endothelium ,GOLD ,EPITHELIAL cells ,FISH physiology ,IMMUNOCHEMISTRY - Abstract
The mammalian bilirubin transporter bilitranslocase (BTL, T.C.#2.A.65.1.1) is found in both absorptive (intestine) and excretory epithelia (liver, kidney) and in the vascular endothelium. The aim of this work was to investigate whether a BTL homologue is expressed also in fish hepatopancreas. Immunochemistry based on an antisequence antibody specific for rat liver BTL demonstrated the presence of such homologue in sea-bass (Dicentrarchus labrax) hepatopancreas. Furthermore the transport activity of such a carrier, measured as electrogenic bromosulphophthalein (BSP) uptake, was assayed in sea-bass microsomes, where it was inhibited by the same antibody. Transport activity in fish showed numerous kinetic similarities with rat, such as BSP Km(about 5 µM in both), bilirubin Ki (about 0.1 µM), quercetin competitive Ki (about 20 µM), and noncompetitive Ki (about 85 µM). Biliverdin Ki was instead nearly 10-fold higher in fish than in rat (0.97 ± 0.06 µM and 0.11 ± 0.01 µM, respectively). Fish BTL was found to exist in two different allosteric forms with different affinities for the substrate, similarly to rat liver BTL. It was found that sea-bass BTL is very sensitive to inhibition by HgCl2, a major water pollutant, making it reasonable to exploit fish BTL activity as an ecotoxicological biosensor. [ABSTRACT FROM PUBLISHER]
- Published
- 2011
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