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Striatal Transcriptome Reveals Differences Between Cognitively Impaired and Unimpaired Aged Male Rats

Cognitive processes require striatal activity. The underlying molecular mechanisms are widely unknown. For this reason the striatal transcriptome of young (YM), aged cognitively impaired (OMB), and unimpaired (OMG) male rats was analyzed. The global comparison of transcripts reveal a higher number o...

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Autores principales: Korz, Volker, Kremslehner, Christopher, Maliković, Jovana, Hussein, Ahmed, Feyissa, Daniel Daba, Nagelreiter, Ionela-Mariana, Smidak, Roman, Plasenzotti, Roberto, Gruber, Florian, Lubec, Gert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7820756/
https://www.ncbi.nlm.nih.gov/pubmed/33488384
http://dx.doi.org/10.3389/fnagi.2020.611572
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author Korz, Volker
Kremslehner, Christopher
Maliković, Jovana
Hussein, Ahmed
Feyissa, Daniel Daba
Nagelreiter, Ionela-Mariana
Smidak, Roman
Plasenzotti, Roberto
Gruber, Florian
Lubec, Gert
author_facet Korz, Volker
Kremslehner, Christopher
Maliković, Jovana
Hussein, Ahmed
Feyissa, Daniel Daba
Nagelreiter, Ionela-Mariana
Smidak, Roman
Plasenzotti, Roberto
Gruber, Florian
Lubec, Gert
author_sort Korz, Volker
collection PubMed
description Cognitive processes require striatal activity. The underlying molecular mechanisms are widely unknown. For this reason the striatal transcriptome of young (YM), aged cognitively impaired (OMB), and unimpaired (OMG) male rats was analyzed. The global comparison of transcripts reveal a higher number of differences between OMG and YM as compared to OMB and YM. Hierarchical clustering detects differences in up- and down-regulated gene clusters in OMG and OMB when compared to YM. In OMG we found more single genes to be specifically regulated in this group than in OMB when compared to young. These genes were considered as cognition specific, whereas genes shared in OMG and OMB were considered as age specific. OMB specific up-regulated genes are related to negative control of cell differentiation and transcription (Hopx), to phagocytosis (Cd202) and cell adhesion (Pcdhb21), whereas down-regulated genes are related to associative learning, behavioral fear response and synaptic transmission (Gabra5). OMG specific up-regulated genes are in the context of maintenance of transcription and estrogen receptor signaling (Padi2, Anxa3), signal transduction [Rassf4, Dock8)], sterol regulation (Srebf1), and complement activity (C4a, C4b). Down-regulated genes are related to lipid oxidation reduction processes (Far2) and positive regulation of axon extension (Islr2). These relations were supported by pathway analysis, which reveals cholesterol metabolism processes in both aged group and cholesterol biosynthesis specifically in OMG; adipogenesis and focal adhesion in OMB. In OMG glucuronidation, estrogen metabolism, inflammatory responses and TGF beta signaling where detected as specific for this group. Signal transduction of the sphingosine-1-phospate-receptor (S1P) receptor was the main pathway difference in the comparison of OMB and OMG with downregulated genes in the first group. This difference could also be observed in the OMB vs. YM comparison but not in the OMG vs. YM analysis. Thus, an up-regulation of cognition related genes could be observed in OMG compared to OMB rats. The S1P pathway discriminated between OMB and OMG as well as between OMB and OMG. Since this pathway has been described as essential for cognitive processes in the striatum of mice, it may, among steroid hormone signaling, significantly contribute to the maintenance of cognitive processes in OMG.
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spelling pubmed-78207562021-01-23 Striatal Transcriptome Reveals Differences Between Cognitively Impaired and Unimpaired Aged Male Rats Korz, Volker Kremslehner, Christopher Maliković, Jovana Hussein, Ahmed Feyissa, Daniel Daba Nagelreiter, Ionela-Mariana Smidak, Roman Plasenzotti, Roberto Gruber, Florian Lubec, Gert Front Aging Neurosci Neuroscience Cognitive processes require striatal activity. The underlying molecular mechanisms are widely unknown. For this reason the striatal transcriptome of young (YM), aged cognitively impaired (OMB), and unimpaired (OMG) male rats was analyzed. The global comparison of transcripts reveal a higher number of differences between OMG and YM as compared to OMB and YM. Hierarchical clustering detects differences in up- and down-regulated gene clusters in OMG and OMB when compared to YM. In OMG we found more single genes to be specifically regulated in this group than in OMB when compared to young. These genes were considered as cognition specific, whereas genes shared in OMG and OMB were considered as age specific. OMB specific up-regulated genes are related to negative control of cell differentiation and transcription (Hopx), to phagocytosis (Cd202) and cell adhesion (Pcdhb21), whereas down-regulated genes are related to associative learning, behavioral fear response and synaptic transmission (Gabra5). OMG specific up-regulated genes are in the context of maintenance of transcription and estrogen receptor signaling (Padi2, Anxa3), signal transduction [Rassf4, Dock8)], sterol regulation (Srebf1), and complement activity (C4a, C4b). Down-regulated genes are related to lipid oxidation reduction processes (Far2) and positive regulation of axon extension (Islr2). These relations were supported by pathway analysis, which reveals cholesterol metabolism processes in both aged group and cholesterol biosynthesis specifically in OMG; adipogenesis and focal adhesion in OMB. In OMG glucuronidation, estrogen metabolism, inflammatory responses and TGF beta signaling where detected as specific for this group. Signal transduction of the sphingosine-1-phospate-receptor (S1P) receptor was the main pathway difference in the comparison of OMB and OMG with downregulated genes in the first group. This difference could also be observed in the OMB vs. YM comparison but not in the OMG vs. YM analysis. Thus, an up-regulation of cognition related genes could be observed in OMG compared to OMB rats. The S1P pathway discriminated between OMB and OMG as well as between OMB and OMG. Since this pathway has been described as essential for cognitive processes in the striatum of mice, it may, among steroid hormone signaling, significantly contribute to the maintenance of cognitive processes in OMG. Frontiers Media S.A. 2021-01-08 /pmc/articles/PMC7820756/ /pubmed/33488384 http://dx.doi.org/10.3389/fnagi.2020.611572 Text en Copyright © 2021 Korz, Kremslehner, Maliković, Hussein, Feyissa, Nagelreiter, Smidak, Plasenzotti, Gruber and Lubec. 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) and the copyright owner(s) 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
Korz, Volker
Kremslehner, Christopher
Maliković, Jovana
Hussein, Ahmed
Feyissa, Daniel Daba
Nagelreiter, Ionela-Mariana
Smidak, Roman
Plasenzotti, Roberto
Gruber, Florian
Lubec, Gert
Striatal Transcriptome Reveals Differences Between Cognitively Impaired and Unimpaired Aged Male Rats
title Striatal Transcriptome Reveals Differences Between Cognitively Impaired and Unimpaired Aged Male Rats
title_full Striatal Transcriptome Reveals Differences Between Cognitively Impaired and Unimpaired Aged Male Rats
title_fullStr Striatal Transcriptome Reveals Differences Between Cognitively Impaired and Unimpaired Aged Male Rats
title_full_unstemmed Striatal Transcriptome Reveals Differences Between Cognitively Impaired and Unimpaired Aged Male Rats
title_short Striatal Transcriptome Reveals Differences Between Cognitively Impaired and Unimpaired Aged Male Rats
title_sort striatal transcriptome reveals differences between cognitively impaired and unimpaired aged male rats
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7820756/
https://www.ncbi.nlm.nih.gov/pubmed/33488384
http://dx.doi.org/10.3389/fnagi.2020.611572
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