Cargando…

Data for mitochondrial proteomic alterations in the aging mouse brain

Mitochondria are dynamic organelles critical for many cellular processes, including energy generation. Thus, mitochondrial dysfunction likely plays a role in the observed alterations in brain glucose metabolism during aging. Despite implications of mitochondrial alterations during brain aging, compr...

Descripción completa

Detalles Bibliográficos
Autores principales: Stauch, Kelly L., Purnell, Phillip R., Villeneuve, Lance M., Fox, Howard S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4510433/
https://www.ncbi.nlm.nih.gov/pubmed/26217775
http://dx.doi.org/10.1016/j.dib.2015.05.004
_version_ 1782382167677992960
author Stauch, Kelly L.
Purnell, Phillip R.
Villeneuve, Lance M.
Fox, Howard S.
author_facet Stauch, Kelly L.
Purnell, Phillip R.
Villeneuve, Lance M.
Fox, Howard S.
author_sort Stauch, Kelly L.
collection PubMed
description Mitochondria are dynamic organelles critical for many cellular processes, including energy generation. Thus, mitochondrial dysfunction likely plays a role in the observed alterations in brain glucose metabolism during aging. Despite implications of mitochondrial alterations during brain aging, comprehensive quantitative proteomic studies remain limited. Therefore, to characterize the global age-associated mitochondrial proteomic changes in the brain, we analyzed mitochondria isolated from the brain of 5-, 12-, and 24-month old mice using quantitative mass spectrometry. We identified changes in the expression of proteins important for biological processes involved in the generation of precursor metabolites and energy through the breakdown of carbohydrates, lipids, and proteins. These results are significant because we identified age-associated proteomic changes suggestive of altered mitochondrial catabolic reactions during brain aging. The proteomic data described here can be found in the PRIDE Archive using the reference number PXD001370. A more comprehensive analysis of this data may be obtained from the article “Proteomic analysis and functional characterization of mouse brain mitochondria during aging reveal alterations in energy metabolism” in PROTEOMICS.
format Online
Article
Text
id pubmed-4510433
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-45104332015-07-27 Data for mitochondrial proteomic alterations in the aging mouse brain Stauch, Kelly L. Purnell, Phillip R. Villeneuve, Lance M. Fox, Howard S. Data Brief Data Article Mitochondria are dynamic organelles critical for many cellular processes, including energy generation. Thus, mitochondrial dysfunction likely plays a role in the observed alterations in brain glucose metabolism during aging. Despite implications of mitochondrial alterations during brain aging, comprehensive quantitative proteomic studies remain limited. Therefore, to characterize the global age-associated mitochondrial proteomic changes in the brain, we analyzed mitochondria isolated from the brain of 5-, 12-, and 24-month old mice using quantitative mass spectrometry. We identified changes in the expression of proteins important for biological processes involved in the generation of precursor metabolites and energy through the breakdown of carbohydrates, lipids, and proteins. These results are significant because we identified age-associated proteomic changes suggestive of altered mitochondrial catabolic reactions during brain aging. The proteomic data described here can be found in the PRIDE Archive using the reference number PXD001370. A more comprehensive analysis of this data may be obtained from the article “Proteomic analysis and functional characterization of mouse brain mitochondria during aging reveal alterations in energy metabolism” in PROTEOMICS. Elsevier 2015-05-21 /pmc/articles/PMC4510433/ /pubmed/26217775 http://dx.doi.org/10.1016/j.dib.2015.05.004 Text en © 2015 Published by Elsevier Inc. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Data Article
Stauch, Kelly L.
Purnell, Phillip R.
Villeneuve, Lance M.
Fox, Howard S.
Data for mitochondrial proteomic alterations in the aging mouse brain
title Data for mitochondrial proteomic alterations in the aging mouse brain
title_full Data for mitochondrial proteomic alterations in the aging mouse brain
title_fullStr Data for mitochondrial proteomic alterations in the aging mouse brain
title_full_unstemmed Data for mitochondrial proteomic alterations in the aging mouse brain
title_short Data for mitochondrial proteomic alterations in the aging mouse brain
title_sort data for mitochondrial proteomic alterations in the aging mouse brain
topic Data Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4510433/
https://www.ncbi.nlm.nih.gov/pubmed/26217775
http://dx.doi.org/10.1016/j.dib.2015.05.004
work_keys_str_mv AT stauchkellyl dataformitochondrialproteomicalterationsintheagingmousebrain
AT purnellphillipr dataformitochondrialproteomicalterationsintheagingmousebrain
AT villeneuvelancem dataformitochondrialproteomicalterationsintheagingmousebrain
AT foxhowards dataformitochondrialproteomicalterationsintheagingmousebrain