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人类肝脏中基因表达的决定因素:衰老和性别对外源物质代谢的影响。

Determinants of gene expression in the human liver: Impact of aging and sex on xenobiotic metabolism.

机构信息

Center for Computational Toxicology and Exposure, US EPA, Research Triangle Park, NC 27711, United States of America.

Center for Public Health and Environmental Assessment, US EPA, Research Triangle Park, NC 27711, United States of America.

出版信息

Exp Gerontol. 2022 Nov;169:111976. doi: 10.1016/j.exger.2022.111976. Epub 2022 Oct 13.

Abstract

There is a need to characterize the potential susceptibility of older adults to toxicity from environmental chemical exposures. Liver xenobiotic metabolizing enzymes (XMEs) play important roles in detoxifying and eliminating xenobiotics. We examined global gene expression in the livers of young (21-45 years) and old (69+ years) men and women. Differentially expressed genes (DEG) were identified using two-way ANOVA (p ≤ 0.05). We identified 1437 and 1670 DEGs between young and old groups in men and women, respectively. Only a minor number of the total number of genes overlapped (146 genes). Aging increased or decreased pathways involved in inflammation and intermediary metabolism, respectively. Aging led to numerous changes in the expression of XME genes or genes known to control their expression (~90 genes). Out of 10 cytochrome P450s activities examined, there were increased activities of CYP1A2 and CYP2C9 enzymes in the old groups. We also identified sex-dependent genes that were more numerous in the young group (1065) than in the old group (202) and included changes in XMEs. These studies indicate that the livers from aging humans when compared to younger adults exhibit changes in XMEs that may lead to differences in the metabolism of xenobiotics.

摘要

需要描述老年人对环境化学暴露毒性的潜在易感性。肝脏外源生物代谢酶 (XMEs) 在解毒和消除外源生物方面发挥着重要作用。我们研究了年轻(21-45 岁)和老年(69 岁以上)男性和女性肝脏中的全局基因表达。使用双因素方差分析 (p≤0.05) 鉴定差异表达基因 (DEG)。我们分别在男性和女性中鉴定出 1437 和 1670 个 DEG。总基因数量中只有一小部分重叠(146 个基因)。衰老分别增加或减少了炎症和中间代谢途径。衰老导致 XME 基因或控制其表达的基因(约 90 个基因)的表达发生了许多变化。在检查的 10 种细胞色素 P450 活性中,老年组 CYP1A2 和 CYP2C9 酶的活性增加。我们还鉴定了性别依赖性基因,这些基因在年轻组(1065 个)中比老年组(202 个)更多,包括 XME 的变化。这些研究表明,与年轻人相比,衰老个体的肝脏在外源生物代谢酶方面发生了变化,这可能导致外源生物代谢的差异。

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