Cargando…
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...
Autores principales: | , , , , , , , , , , |
---|---|
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 |
_version_ | 1783287190047948800 |
---|---|
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. |
format | Online Article Text |
id | pubmed-5735351 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT wangjiao biosystemsstudyofthemolecularnetworksunderlyinghippocampalagingprogressionandantiagingtreatmentinmice AT liqian biosystemsstudyofthemolecularnetworksunderlyinghippocampalagingprogressionandantiagingtreatmentinmice AT kongyanyan biosystemsstudyofthemolecularnetworksunderlyinghippocampalagingprogressionandantiagingtreatmentinmice AT zhoufangfang biosystemsstudyofthemolecularnetworksunderlyinghippocampalagingprogressionandantiagingtreatmentinmice AT lijie biosystemsstudyofthemolecularnetworksunderlyinghippocampalagingprogressionandantiagingtreatmentinmice AT liweihao biosystemsstudyofthemolecularnetworksunderlyinghippocampalagingprogressionandantiagingtreatmentinmice AT wangkai biosystemsstudyofthemolecularnetworksunderlyinghippocampalagingprogressionandantiagingtreatmentinmice AT wuting biosystemsstudyofthemolecularnetworksunderlyinghippocampalagingprogressionandantiagingtreatmentinmice AT guanyihui biosystemsstudyofthemolecularnetworksunderlyinghippocampalagingprogressionandantiagingtreatmentinmice AT xiejiang biosystemsstudyofthemolecularnetworksunderlyinghippocampalagingprogressionandantiagingtreatmentinmice AT wentieqiao biosystemsstudyofthemolecularnetworksunderlyinghippocampalagingprogressionandantiagingtreatmentinmice |