CO-EXPRESSION OF GCDH AND OAT1 IN NEURONS AND PROXIMAL TUBULE CELLS

Details

Serval ID
serval:BIB_689ED77047BD
Type
Inproceedings: an article in a conference proceedings.
Publication sub-type
Poster: Summary – with images – on one page of the results of a researche project. The summaries of the poster must be entered in "Abstract" and not "Poster".
Collection
Publications
Institution
Title
CO-EXPRESSION OF GCDH AND OAT1 IN NEURONS AND PROXIMAL TUBULE CELLS
Title of the conference
Annual Symposium of the Society for the Study of Inborn Errors of Metabolism
Author(s)
Ballhausen D., Jafari P., Bonafe L., Braissant O.
Address
Geneva, Switzerland, August 30-September 2, 2011
ISBN
0141-8955
Publication state
Published
Issued date
2011
Volume
34
Series
Journal of Inherited Metabolic Diseases
Pages
S141
Language
english
Notes
Document Type:Meeting Abstract
Abstract
Tissue-specific expression studies of Glutaryl-CoA dehydrogenase (Gcdh)
in adult rats revealed expression in the whole rat brain, almost exclusively
in neurons, and surprisingly high expression in the juxtamedullar cortex of
the kidney. The organic anion transporter 1 (OAT1) mediates basolateral
uptake of glutarate derivatives from proximal tubule cells and contributes
to their renal clearance. In brain, OAT1 is expressed at the choroid plexus,
in neurons of cortex and hippocampus. We hypothesized that Gcdh and
Oat1 are co-expressed in the same cells in kidney and brain and analyzed
their mRNA expression by in situ hybridization on cryosections of adult rat
brain, kidney and liver. In brain, Gcdh and Oat1 were found co-expressed
in most neurons. Only the Purkinje neurons of the cerebellum were found
to be Oat1 negative. In the kidney Gcdh and Oat1 are widely co-expressed
with a specific high expression in proximal tubule cells. In conclusion
there seems to be a functional coupling of Gcdh and Oat1 on a renal and
neuronal level. Further studies are ongoing to confirm these findings in
human tissues.
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Create date
14/02/2014 17:27
Last modification date
20/08/2019 14:23
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