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Biosystems Study of the Molecular Networks Underlying Hippocampal Aging Progression and Anti-aging Treatment in Mice

Aging progression is a process that an individual encounters as they become older, and usually results from a series of normal physiological changes over time. The hippocampus, which contributes to the loss of spatial and episodic memory and learning in older people, is closely related to the detrim...

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Autores principales: Wang, Jiao, Li, Qian, Kong, Yanyan, Zhou, Fangfang, Li, Jie, Li, Weihao, Wang, Kai, Wu, Ting, Guan, Yihui, Xie, Jiang, Wen, Tieqiao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5735351/
https://www.ncbi.nlm.nih.gov/pubmed/29311893
http://dx.doi.org/10.3389/fnagi.2017.00393
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author Wang, Jiao
Li, Qian
Kong, Yanyan
Zhou, Fangfang
Li, Jie
Li, Weihao
Wang, Kai
Wu, Ting
Guan, Yihui
Xie, Jiang
Wen, Tieqiao
author_facet Wang, Jiao
Li, Qian
Kong, Yanyan
Zhou, Fangfang
Li, Jie
Li, Weihao
Wang, Kai
Wu, Ting
Guan, Yihui
Xie, Jiang
Wen, Tieqiao
author_sort Wang, Jiao
collection PubMed
description Aging progression is a process that an individual encounters as they become older, and usually results from a series of normal physiological changes over time. The hippocampus, which contributes to the loss of spatial and episodic memory and learning in older people, is closely related to the detrimental effects of aging at the morphological and molecular levels. However, age-related genetic changes in hippocampal molecular mechanisms are not yet well-established. To provide additional insight into the aging process, differentially-expressed genes of 3- versus 24- and 29-month old mice were re-analyzed. The results revealed that a large number of immune and inflammatory response-related genes were up-regulated in the aged hippocampus, and membrane receptor-associated genes were down-regulated. The down-regulation of transmembrane receptors may indicate the weaker perception of environmental exposure in older people, since many transmembrane proteins participate in signal transduction. In addition, molecular interaction analysis of the up-regulated immune genes indicated that the hub gene, Ywhae, may play essential roles in immune and inflammatory responses during aging progression, as well as during hippocampal development. Our biological experiments confirmed the conserved roles of Ywhae and its partners between human and mouse. Furthermore, comparison of microarray data between advanced-age mice treated with human umbilical cord blood plasma protein and the phosphate-buffered saline control showed that the genes that contribute to the revitalization of advanced-age mice are different from the genes induced by aging. These results implied that the revitalization of advanced-age mice is not a simple reverse process of normal aging progression. Our data assigned novel roles of genes during aging progression and provided further theoretic evidence for future studies exploring the underlying mechanisms of aging and anti-aging-related disease therapy.
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spelling pubmed-57353512018-01-08 Biosystems Study of the Molecular Networks Underlying Hippocampal Aging Progression and Anti-aging Treatment in Mice Wang, Jiao Li, Qian Kong, Yanyan Zhou, Fangfang Li, Jie Li, Weihao Wang, Kai Wu, Ting Guan, Yihui Xie, Jiang Wen, Tieqiao Front Aging Neurosci Neuroscience Aging progression is a process that an individual encounters as they become older, and usually results from a series of normal physiological changes over time. The hippocampus, which contributes to the loss of spatial and episodic memory and learning in older people, is closely related to the detrimental effects of aging at the morphological and molecular levels. However, age-related genetic changes in hippocampal molecular mechanisms are not yet well-established. To provide additional insight into the aging process, differentially-expressed genes of 3- versus 24- and 29-month old mice were re-analyzed. The results revealed that a large number of immune and inflammatory response-related genes were up-regulated in the aged hippocampus, and membrane receptor-associated genes were down-regulated. The down-regulation of transmembrane receptors may indicate the weaker perception of environmental exposure in older people, since many transmembrane proteins participate in signal transduction. In addition, molecular interaction analysis of the up-regulated immune genes indicated that the hub gene, Ywhae, may play essential roles in immune and inflammatory responses during aging progression, as well as during hippocampal development. Our biological experiments confirmed the conserved roles of Ywhae and its partners between human and mouse. Furthermore, comparison of microarray data between advanced-age mice treated with human umbilical cord blood plasma protein and the phosphate-buffered saline control showed that the genes that contribute to the revitalization of advanced-age mice are different from the genes induced by aging. These results implied that the revitalization of advanced-age mice is not a simple reverse process of normal aging progression. Our data assigned novel roles of genes during aging progression and provided further theoretic evidence for future studies exploring the underlying mechanisms of aging and anti-aging-related disease therapy. Frontiers Media S.A. 2017-12-06 /pmc/articles/PMC5735351/ /pubmed/29311893 http://dx.doi.org/10.3389/fnagi.2017.00393 Text en Copyright © 2017 Wang, Li, Kong, Zhou, Li, Li, Wang, Wu, Guan, Xie and Wen. 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
Wang, Jiao
Li, Qian
Kong, Yanyan
Zhou, Fangfang
Li, Jie
Li, Weihao
Wang, Kai
Wu, Ting
Guan, Yihui
Xie, Jiang
Wen, Tieqiao
Biosystems Study of the Molecular Networks Underlying Hippocampal Aging Progression and Anti-aging Treatment in Mice
title Biosystems Study of the Molecular Networks Underlying Hippocampal Aging Progression and Anti-aging Treatment in Mice
title_full Biosystems Study of the Molecular Networks Underlying Hippocampal Aging Progression and Anti-aging Treatment in Mice
title_fullStr Biosystems Study of the Molecular Networks Underlying Hippocampal Aging Progression and Anti-aging Treatment in Mice
title_full_unstemmed Biosystems Study of the Molecular Networks Underlying Hippocampal Aging Progression and Anti-aging Treatment in Mice
title_short Biosystems Study of the Molecular Networks Underlying Hippocampal Aging Progression and Anti-aging Treatment in Mice
title_sort biosystems study of the molecular networks underlying hippocampal aging progression and anti-aging treatment in mice
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5735351/
https://www.ncbi.nlm.nih.gov/pubmed/29311893
http://dx.doi.org/10.3389/fnagi.2017.00393
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