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Blood transcriptome analysis revealing aging gene expression profiles in red panda

The red panda is an endangered forest species distributed on the edge of the Qinghai Tibet Plateau. The species has been conserved in ex-situ in many countries and its survival is threatened by many diseases. Its immune system is vulnerable to age-associated alterations, which accumulate and result...

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Autores principales: Luo, Jing, Zhang, Liang, Shen, Fujun, Luo, Li, Chen, Lei, Fan, Zhenxin, Hou, Rong, Yue, Bisong, Zhang, Xiuyue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9310792/
https://www.ncbi.nlm.nih.gov/pubmed/35898935
http://dx.doi.org/10.7717/peerj.13743
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author Luo, Jing
Zhang, Liang
Shen, Fujun
Luo, Li
Chen, Lei
Fan, Zhenxin
Hou, Rong
Yue, Bisong
Zhang, Xiuyue
author_facet Luo, Jing
Zhang, Liang
Shen, Fujun
Luo, Li
Chen, Lei
Fan, Zhenxin
Hou, Rong
Yue, Bisong
Zhang, Xiuyue
author_sort Luo, Jing
collection PubMed
description The red panda is an endangered forest species distributed on the edge of the Qinghai Tibet Plateau. The species has been conserved in ex-situ in many countries and its survival is threatened by many diseases. Its immune system is vulnerable to age-associated alterations, which accumulate and result in a progressive deterioration that leads to an increased incidence of diseases. We identified 2,219 differentially expressed genes (DEGs) between geriatric (11–16 years) and adult individuals (4–8 years), and 1690 DEGs between adults and juveniles (1 year). The gene expression and functional annotation results showed that the innate immunity of red pandas increases significantly in geriatric individuals, whereas its change remains unclear when comparing adults and juveniles. We found that the adaptive immunity of red pandas first increased and then decreased with age. We identified CXCR3, BLNK, and CCR4 as the hub genes in the age-related protein–protein interaction network, which showed their central role in age-related immune changes. Many DNA repair genes were down-regulated in geriatric red pandas, suggesting that the DNA repair ability of the blood tissue in geriatric red pandas is significantly reduced. The significantly up-regulated TLR5 in geriatric individuals also suggests the possibility of enhancing the vaccination immune response by incorporating flagellin, which could be used to address decreased vaccine responses caused by age-related declines in immune system function. This work provides an insight into gene expression changes associated with aging and paves the way for effective disease prevention and treatment strategies for red pandas in the future.
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spelling pubmed-93107922022-07-26 Blood transcriptome analysis revealing aging gene expression profiles in red panda Luo, Jing Zhang, Liang Shen, Fujun Luo, Li Chen, Lei Fan, Zhenxin Hou, Rong Yue, Bisong Zhang, Xiuyue PeerJ Bioinformatics The red panda is an endangered forest species distributed on the edge of the Qinghai Tibet Plateau. The species has been conserved in ex-situ in many countries and its survival is threatened by many diseases. Its immune system is vulnerable to age-associated alterations, which accumulate and result in a progressive deterioration that leads to an increased incidence of diseases. We identified 2,219 differentially expressed genes (DEGs) between geriatric (11–16 years) and adult individuals (4–8 years), and 1690 DEGs between adults and juveniles (1 year). The gene expression and functional annotation results showed that the innate immunity of red pandas increases significantly in geriatric individuals, whereas its change remains unclear when comparing adults and juveniles. We found that the adaptive immunity of red pandas first increased and then decreased with age. We identified CXCR3, BLNK, and CCR4 as the hub genes in the age-related protein–protein interaction network, which showed their central role in age-related immune changes. Many DNA repair genes were down-regulated in geriatric red pandas, suggesting that the DNA repair ability of the blood tissue in geriatric red pandas is significantly reduced. The significantly up-regulated TLR5 in geriatric individuals also suggests the possibility of enhancing the vaccination immune response by incorporating flagellin, which could be used to address decreased vaccine responses caused by age-related declines in immune system function. This work provides an insight into gene expression changes associated with aging and paves the way for effective disease prevention and treatment strategies for red pandas in the future. PeerJ Inc. 2022-07-22 /pmc/articles/PMC9310792/ /pubmed/35898935 http://dx.doi.org/10.7717/peerj.13743 Text en ©2022 Luo et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Bioinformatics
Luo, Jing
Zhang, Liang
Shen, Fujun
Luo, Li
Chen, Lei
Fan, Zhenxin
Hou, Rong
Yue, Bisong
Zhang, Xiuyue
Blood transcriptome analysis revealing aging gene expression profiles in red panda
title Blood transcriptome analysis revealing aging gene expression profiles in red panda
title_full Blood transcriptome analysis revealing aging gene expression profiles in red panda
title_fullStr Blood transcriptome analysis revealing aging gene expression profiles in red panda
title_full_unstemmed Blood transcriptome analysis revealing aging gene expression profiles in red panda
title_short Blood transcriptome analysis revealing aging gene expression profiles in red panda
title_sort blood transcriptome analysis revealing aging gene expression profiles in red panda
topic Bioinformatics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9310792/
https://www.ncbi.nlm.nih.gov/pubmed/35898935
http://dx.doi.org/10.7717/peerj.13743
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