Cargando…

The Neuronal and Peripheral Expressed Membrane-Bound UNC93A Respond to Nutrient Availability in Mice

Many transporters such as the solute carriers belonging to the Major facilitator superfamily Pfam clan are orphans in that their tissue and cellular localization as well as substrate profile and function are still unknown. Here we have characterized the putative solute carrier UNC93A. We aimed to in...

Descripción completa

Detalles Bibliográficos
Autores principales: Ceder, Mikaela M., Lekholm, Emilia, Hellsten, Sofie V., Perland, Emelie, Fredriksson, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5671512/
https://www.ncbi.nlm.nih.gov/pubmed/29163028
http://dx.doi.org/10.3389/fnmol.2017.00351
_version_ 1783276247581720576
author Ceder, Mikaela M.
Lekholm, Emilia
Hellsten, Sofie V.
Perland, Emelie
Fredriksson, Robert
author_facet Ceder, Mikaela M.
Lekholm, Emilia
Hellsten, Sofie V.
Perland, Emelie
Fredriksson, Robert
author_sort Ceder, Mikaela M.
collection PubMed
description Many transporters such as the solute carriers belonging to the Major facilitator superfamily Pfam clan are orphans in that their tissue and cellular localization as well as substrate profile and function are still unknown. Here we have characterized the putative solute carrier UNC93A. We aimed to investigate the expression profile on both protein and mRNA level of UNC93A in mouse since it has not been clarified. UNC93A staining was found in cortex, hippocampus and cerebellum. It was found to be expressed in many neurons, but not all, with staining located in close proximity to the plasma membrane. Furthermore, we aimed to extend the starvation data available for Unc93a in hypothalamic cell cultures from mouse. We investigated the Unc93a alterations with focus on amino acid deprivation in embryonic cortex cells from mice as well as 24 h starvation in adult male mice and compared it to recently studied putative and known solute carriers. Unc93a expression was found both in the brain and peripheral organs, in low to moderate levels in the adult mice and was affected by amino acid deprivation in embryonic cortex cultures and starvation in in vivo samples. In conclusion, the membrane-bound UNC93A is expressed in both the brain and peripheral tissues and responds to nutrient availability in mice.
format Online
Article
Text
id pubmed-5671512
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-56715122017-11-21 The Neuronal and Peripheral Expressed Membrane-Bound UNC93A Respond to Nutrient Availability in Mice Ceder, Mikaela M. Lekholm, Emilia Hellsten, Sofie V. Perland, Emelie Fredriksson, Robert Front Mol Neurosci Neuroscience Many transporters such as the solute carriers belonging to the Major facilitator superfamily Pfam clan are orphans in that their tissue and cellular localization as well as substrate profile and function are still unknown. Here we have characterized the putative solute carrier UNC93A. We aimed to investigate the expression profile on both protein and mRNA level of UNC93A in mouse since it has not been clarified. UNC93A staining was found in cortex, hippocampus and cerebellum. It was found to be expressed in many neurons, but not all, with staining located in close proximity to the plasma membrane. Furthermore, we aimed to extend the starvation data available for Unc93a in hypothalamic cell cultures from mouse. We investigated the Unc93a alterations with focus on amino acid deprivation in embryonic cortex cells from mice as well as 24 h starvation in adult male mice and compared it to recently studied putative and known solute carriers. Unc93a expression was found both in the brain and peripheral organs, in low to moderate levels in the adult mice and was affected by amino acid deprivation in embryonic cortex cultures and starvation in in vivo samples. In conclusion, the membrane-bound UNC93A is expressed in both the brain and peripheral tissues and responds to nutrient availability in mice. Frontiers Media S.A. 2017-10-31 /pmc/articles/PMC5671512/ /pubmed/29163028 http://dx.doi.org/10.3389/fnmol.2017.00351 Text en Copyright © 2017 Ceder, Lekholm, Hellsten, Perland and Fredriksson. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Ceder, Mikaela M.
Lekholm, Emilia
Hellsten, Sofie V.
Perland, Emelie
Fredriksson, Robert
The Neuronal and Peripheral Expressed Membrane-Bound UNC93A Respond to Nutrient Availability in Mice
title The Neuronal and Peripheral Expressed Membrane-Bound UNC93A Respond to Nutrient Availability in Mice
title_full The Neuronal and Peripheral Expressed Membrane-Bound UNC93A Respond to Nutrient Availability in Mice
title_fullStr The Neuronal and Peripheral Expressed Membrane-Bound UNC93A Respond to Nutrient Availability in Mice
title_full_unstemmed The Neuronal and Peripheral Expressed Membrane-Bound UNC93A Respond to Nutrient Availability in Mice
title_short The Neuronal and Peripheral Expressed Membrane-Bound UNC93A Respond to Nutrient Availability in Mice
title_sort neuronal and peripheral expressed membrane-bound unc93a respond to nutrient availability in mice
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5671512/
https://www.ncbi.nlm.nih.gov/pubmed/29163028
http://dx.doi.org/10.3389/fnmol.2017.00351
work_keys_str_mv AT cedermikaelam theneuronalandperipheralexpressedmembraneboundunc93arespondtonutrientavailabilityinmice
AT lekholmemilia theneuronalandperipheralexpressedmembraneboundunc93arespondtonutrientavailabilityinmice
AT hellstensofiev theneuronalandperipheralexpressedmembraneboundunc93arespondtonutrientavailabilityinmice
AT perlandemelie theneuronalandperipheralexpressedmembraneboundunc93arespondtonutrientavailabilityinmice
AT fredrikssonrobert theneuronalandperipheralexpressedmembraneboundunc93arespondtonutrientavailabilityinmice
AT cedermikaelam neuronalandperipheralexpressedmembraneboundunc93arespondtonutrientavailabilityinmice
AT lekholmemilia neuronalandperipheralexpressedmembraneboundunc93arespondtonutrientavailabilityinmice
AT hellstensofiev neuronalandperipheralexpressedmembraneboundunc93arespondtonutrientavailabilityinmice
AT perlandemelie neuronalandperipheralexpressedmembraneboundunc93arespondtonutrientavailabilityinmice
AT fredrikssonrobert neuronalandperipheralexpressedmembraneboundunc93arespondtonutrientavailabilityinmice