Molecular cloning and functional characterization of a rainbow trout liver Oatp

Steiner, Konstanze; Hagenbuch, Bruno; Dietrich, Daniel R.

Molecular cloning and functional characterization of a rainbow trout liver Oatp

Dateien

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Datum

2014

Autor:innen

Steiner, Konstanze

Hagenbuch, Bruno

Dietrich, Daniel R.

Open Access-Veröffentlichung

Open Access Green

Sammlungen

Biologie

Publikationstyp

Zeitschriftenartikel

Publikationsstatus

Published

Erschienen in

Toxicology and Applied Pharmacology. 2014, 280(3), pp. 534-542. ISSN 0041-008X. eISSN 1096-0333. Available under: doi: 10.1016/j.taap.2014.08.031

Zusammenfassung

Cyanobacterial blooms have an impact on the aquatic ecosystem due to the production of toxins (e.g. microcystins, MCs), which constrain fish health or even cause fish death. However the toxicokinetics of the most abundant toxin, microcystin-LR (MC-LR), are not yet fully understood. To investigate the uptake mechanism, the novel Oatp1d1 in rainbow trout (rtOatp1d1) was cloned, identified and characterized. The cDNA isolated from a clone library consisted of 2772 bp containing a 2115 bp open reading frame coding for a 705 aa protein with an approximate molecular mass of 80 kDa. This fish specific transporter belongs to the OATP1 family and has most likely evolved from a common ancestor of OATP1C1. Real time PCR analysis showed that rtOatp1d1 is predominantly expressed in the liver, followed by the brain while expression in other organs was not detectable. Transient transfection in HEK293 cells was used for further characterization. Like its human homologues OATP1A1, OATP1B1 and OATP1B3, rtOatp1d1 displayed multi-specific transport including endogenous and xenobiotic substrates. Kinetic analyses revealed a K_m value of 13.9 μM and 13.4 μM for estrone-3-sulfate and methotrexate, respectively and a rather low affinity for taurocholate with a K_m value of 103 μM. Furthermore, it was confirmed that rtOatp1d1 is a MC-LR transporter and therefore most likely plays a key role in the susceptibility of rainbow trout to MC intoxications.

Fachgebiet (DDC)

570 Biowissenschaften, Biologie

Schlagwörter

Microcystin, Oatp, Rainbow trout, Toxin transport

Zitieren

ISO 690

STEINER, Konstanze, Bruno HAGENBUCH, Daniel R. DIETRICH, 2014. Molecular cloning and functional characterization of a rainbow trout liver Oatp. In: Toxicology and Applied Pharmacology. 2014, 280(3), pp. 534-542. ISSN 0041-008X. eISSN 1096-0333. Available under: doi: 10.1016/j.taap.2014.08.031

BibTex

@article{Steiner2014Molec-29433,
  year={2014},
  doi={10.1016/j.taap.2014.08.031},
  title={Molecular cloning and functional characterization of a rainbow trout liver Oatp},
  number={3},
  volume={280},
  issn={0041-008X},
  journal={Toxicology and Applied Pharmacology},
  pages={534--542},
  author={Steiner, Konstanze and Hagenbuch, Bruno and Dietrich, Daniel R.}
}

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    <dcterms:abstract xml:lang="eng">Cyanobacterial blooms have an impact on the aquatic ecosystem due to the production of toxins (e.g. microcystins, MCs), which constrain fish health or even cause fish death. However the toxicokinetics of the most abundant toxin, microcystin-LR (MC-LR), are not yet fully understood. To investigate the uptake mechanism, the novel Oatp1d1 in rainbow trout (rtOatp1d1) was cloned, identified and characterized. The cDNA isolated from a clone library consisted of 2772 bp containing a 2115 bp open reading frame coding for a 705 aa protein with an approximate molecular mass of 80 kDa. This fish specific transporter belongs to the OATP1 family and has most likely evolved from a common ancestor of OATP1C1. Real time PCR analysis showed that rtOatp1d1 is predominantly expressed in the liver, followed by the brain while expression in other organs was not detectable. Transient transfection in HEK293 cells was used for further characterization. Like its human homologues OATP1A1, OATP1B1 and OATP1B3, rtOatp1d1 displayed multi-specific transport including endogenous and xenobiotic substrates. Kinetic analyses revealed a K&lt;sub&gt;m&lt;/sub&gt; value of 13.9 μM and 13.4 μM for estrone-3-sulfate and methotrexate, respectively and a rather low affinity for taurocholate with a K&lt;sub&gt;m&lt;/sub&gt; value of 103 μM. Furthermore, it was confirmed that rtOatp1d1 is a MC-LR transporter and therefore most likely plays a key role in the susceptibility of rainbow trout to MC intoxications.</dcterms:abstract>
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