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pmid:31941443

Proteomics profiling and pathway analysis of hippocampal aging in rhesus monkeys.

Shu Meng · Wenchao Xia · Meng Pan · Yangjie Jia · Zhanlong He · Wei Ge

BMC neuroscience · 2020 doi:10.1186/s12868-020-0550-4

Paper

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Experiment

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Data

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Analysis

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Proteomics profiling and pathway analysis of hippocampal aging in rhesus monkeys.
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10.1186/s12868-020-0550-4
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Shu Meng
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Wenchao Xia
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Meng Pan
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Yangjie Jia
[4]
Zhanlong He
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Wei Ge
journal
BMC neuroscience
year
2020
abstract
BACKGROUND: Aged rhesus monkeys exhibit deficits in memory mediated by the hippocampus. Although extensive research has been carried out on the characteristics of human hippocampal aging, there is still very little scientific understanding of the changes associated with hippocampal aging in rhesus monkeys. To explore the proteomics profiling and pathway-related changes in the rhesus hippocampus during the aging process, we conducted a high throughput quantitative proteomics analysis of hippocampal samples from two groups of rhesus macaques aged 6 years and 20 years, using 2-plex tandem mass tag (TMT) labeling. In addition, we used a comprehensive bioinformatics analysis approach to investigate the enriched signaling pathways of differentially expressed proteins (the ratios of 20-years vs. 6-years, ≥ 1.20 or ≤ 0.83). RESULTS: In total, 3260 proteins were identified with a high level of confidence in rhesus hippocampus. We found 367 differentially expressed proteins related to rhesus hippocampus aging. Based on biological pathway analysis, we found these aging-related proteins were predominantly enriched in the electron transport chain, NRF2 pathway, focal adhesion-PI3K-AKT-mTOR signaling pathway and cytoplasmic ribosome proteins. Data are available via ProteomeXchange with identifier PXD011398. CONCLUSION: This study provides a detail description of the proteomics profile related to rhesus hippocampal aging. These findings should make an important contribution to further mechanistic studies, marker selection and drug development for the prevention and treatment of aging or age-related neurodegeneration.
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Focal adhesion and NRF2 pathway regulate left-right asymmetries of rhesus hippocampus aging: relevance to human hippocampus aging and Alzheimer’s disease
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