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Histological characterization of orphan transporter MCT14 (SLC16A14) shows abundant expression in mouse CNS and kidney

BACKGROUND: MCT14 (SLC16A14) is an orphan member of the monocarboxylate transporter (MCT) family, also known as the SLC16 family of secondary active transmembrane transporters. Available expression data for this transporter is limited, and in this paper we aim to characterize MCT14 with respect to t...

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Autores principales: Roshanbin, Sahar, Lindberg, Frida A., Lekholm, Emilia, Eriksson, Mikaela M., Perland, Emelie, Åhlund, Johan, Raine, Amanda, Fredriksson, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4929735/
https://www.ncbi.nlm.nih.gov/pubmed/27364523
http://dx.doi.org/10.1186/s12868-016-0274-7
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author Roshanbin, Sahar
Lindberg, Frida A.
Lekholm, Emilia
Eriksson, Mikaela M.
Perland, Emelie
Åhlund, Johan
Raine, Amanda
Fredriksson, Robert
author_facet Roshanbin, Sahar
Lindberg, Frida A.
Lekholm, Emilia
Eriksson, Mikaela M.
Perland, Emelie
Åhlund, Johan
Raine, Amanda
Fredriksson, Robert
author_sort Roshanbin, Sahar
collection PubMed
description BACKGROUND: MCT14 (SLC16A14) is an orphan member of the monocarboxylate transporter (MCT) family, also known as the SLC16 family of secondary active transmembrane transporters. Available expression data for this transporter is limited, and in this paper we aim to characterize MCT14 with respect to tissue distribution and cellular localization in mouse brain. RESULTS: Using qPCR, we found that Slc16a14 mRNA was highly abundant in mouse kidney and moderately in central nervous system, testis, uterus and liver. Using immunohistochemistry and in situ hybridization, we determined that MCT14 was highly expressed in excitatory and inhibitory neurons as well as epithelial cells in the mouse brain. The expression was exclusively localized to the soma of neurons. Furthermore, we showed with our phylogenetic analysis that MCT14 most closely relate to the aromatic amino acid- and thyroid-hormone transporters MCT8 (SLC16A2) and MCT10 (SLC16A10), in addition to the carnitine transporter MCT9 (SLC16A9). CONCLUSIONS: We provide here the first histological mapping of MCT14 in the brain and our data are consistent with the hypothesis that MCT14 is a neuronal aromatic-amino-acid transporter. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12868-016-0274-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-49297352016-07-02 Histological characterization of orphan transporter MCT14 (SLC16A14) shows abundant expression in mouse CNS and kidney Roshanbin, Sahar Lindberg, Frida A. Lekholm, Emilia Eriksson, Mikaela M. Perland, Emelie Åhlund, Johan Raine, Amanda Fredriksson, Robert BMC Neurosci Research Article BACKGROUND: MCT14 (SLC16A14) is an orphan member of the monocarboxylate transporter (MCT) family, also known as the SLC16 family of secondary active transmembrane transporters. Available expression data for this transporter is limited, and in this paper we aim to characterize MCT14 with respect to tissue distribution and cellular localization in mouse brain. RESULTS: Using qPCR, we found that Slc16a14 mRNA was highly abundant in mouse kidney and moderately in central nervous system, testis, uterus and liver. Using immunohistochemistry and in situ hybridization, we determined that MCT14 was highly expressed in excitatory and inhibitory neurons as well as epithelial cells in the mouse brain. The expression was exclusively localized to the soma of neurons. Furthermore, we showed with our phylogenetic analysis that MCT14 most closely relate to the aromatic amino acid- and thyroid-hormone transporters MCT8 (SLC16A2) and MCT10 (SLC16A10), in addition to the carnitine transporter MCT9 (SLC16A9). CONCLUSIONS: We provide here the first histological mapping of MCT14 in the brain and our data are consistent with the hypothesis that MCT14 is a neuronal aromatic-amino-acid transporter. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12868-016-0274-7) contains supplementary material, which is available to authorized users. BioMed Central 2016-07-01 /pmc/articles/PMC4929735/ /pubmed/27364523 http://dx.doi.org/10.1186/s12868-016-0274-7 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Roshanbin, Sahar
Lindberg, Frida A.
Lekholm, Emilia
Eriksson, Mikaela M.
Perland, Emelie
Åhlund, Johan
Raine, Amanda
Fredriksson, Robert
Histological characterization of orphan transporter MCT14 (SLC16A14) shows abundant expression in mouse CNS and kidney
title Histological characterization of orphan transporter MCT14 (SLC16A14) shows abundant expression in mouse CNS and kidney
title_full Histological characterization of orphan transporter MCT14 (SLC16A14) shows abundant expression in mouse CNS and kidney
title_fullStr Histological characterization of orphan transporter MCT14 (SLC16A14) shows abundant expression in mouse CNS and kidney
title_full_unstemmed Histological characterization of orphan transporter MCT14 (SLC16A14) shows abundant expression in mouse CNS and kidney
title_short Histological characterization of orphan transporter MCT14 (SLC16A14) shows abundant expression in mouse CNS and kidney
title_sort histological characterization of orphan transporter mct14 (slc16a14) shows abundant expression in mouse cns and kidney
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4929735/
https://www.ncbi.nlm.nih.gov/pubmed/27364523
http://dx.doi.org/10.1186/s12868-016-0274-7
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