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Klonierung und funktionelle Charakterisierung des pOAT1 in ok-Zellen

dc.contributor.advisorHagos, Yohannes Prof. Dr.
dc.contributor.authorSendler, Mark Florian
dc.date.accessioned2015-11-25T09:49:52Z
dc.date.available2015-12-02T23:50:05Z
dc.date.issued2015-11-25
dc.identifier.urihttp://hdl.handle.net/11858/00-1735-0000-0028-8641-A
dc.identifier.urihttp://dx.doi.org/10.53846/goediss-5381
dc.identifier.urihttp://dx.doi.org/10.53846/goediss-5381
dc.language.isodeude
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject.ddc610de
dc.titleKlonierung und funktionelle Charakterisierung des pOAT1 in ok-Zellende
dc.typedoctoralThesisde
dc.title.translatedCloning and functional characterization of the pOAT1 in ok-cellsde
dc.contributor.refereeBohnsack, Markus Prof. Dr.
dc.date.examination2015-11-25
dc.description.abstractengWe created and screened a pig kidney cDNA library for the organic anionen transporter 1 (pOAT1) und could isolate two splice variants (pOAT1: EMBL Acc. AJ308234 and pOAT1A: AJ308235). The functional characterization by expression of pOAT1 in Xenopus laevis oocytes and ok-cells showed an [3H]PAH uptake only for pOAT1. The apparrent Km for [3H]PAH in oocytes is 3,75 ± 1,6 µM and in ok-cells it is 8,54 ± 1,2 µM. This uptake was inhibited by 1mM probenecid and 1mM glutarate. The functional characterization revealed an similar cis inhibition of the pOAT1 mediated uptake for [3H]PAH by pyrazionat, urate, glutarate and probenicid as in pig BLMV. We also could show that the chlorid dependent uptake of [3H]PAH in pig BLMV is mediated by the pOAT1 whereas the chlorid independent urate uptake is mediated by the pOAT3. Testing steroids as substrate for the pOAT1 demonstrated a strong inhibition of the [3H]PAH uptake (Ki for estrone sulfate 113± 4,9µM; Ki for DHEA sulfate 116,5± 3,5µM) whereas [3H]estrone sulfate was not transported by the pOAT1.de
dc.contributor.coRefereeSchön, Margarete Prof. Dr.
dc.subject.gerpOAT1de
dc.subject.gerorganische Anionen Transporterde
dc.subject.gerok-Zellende
dc.subject.gerslc22 Familiede
dc.subject.gerSchweinde
dc.subject.engpOAT1de
dc.subject.engorganic anion transporterde
dc.subject.engok cellsde
dc.subject.engslc22 familyde
dc.subject.engpigde
dc.identifier.urnurn:nbn:de:gbv:7-11858/00-1735-0000-0028-8641-A-6
dc.affiliation.instituteMedizinische Fakultätde
dc.subject.gokfullMedizin (PPN619874732)de
dc.description.embargoed2015-12-02
dc.identifier.ppn840882491


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