肝脏再生对衰老相关基因表达和代谢功能变化的差异影响。

IF 7.1 1区 医学 Q1 CELL BIOLOGY
Aging Cell Pub Date : 2025-08-12 DOI:10.1111/acel.70197
Ryo Murayama, Kenichi Horisawa, Shizuka Miura, Sumiaki Taniguchi, Jinghao Shu, Masatomo Takahashi, Yoshihiro Izumi, Takeshi Bamba, Kousei Ishigami, Atsushi Suzuki
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引用次数: 0

摘要

衰老导致各器官细胞的基因表达和代谢功能发生显著变化。虽然已知衰老会延缓肝脏再生,但衰老对肝脏再生中基因表达和代谢功能变化的影响有待进一步研究。在本研究中,我们综合分析了年轻和老年小鼠肝脏再生过程中基因表达和代谢功能的变化,以探讨衰老对这些变化的影响。在肝再生过程中,幼鼠和老龄鼠肝细胞的基因表达谱在保持相近的情况下呈逐步变化。肝脏再生完成后,老年小鼠肝细胞中具有衰老特异性表达模式的基因的表达水平改变为接近年轻小鼠肝细胞的表达水平。与这些转录组分析的结果相反,在老年小鼠肝脏中检测到的代谢状态的衰老特异性变化在肝脏再生完成后基本保持不变。这些结果表明,老年小鼠肝脏的基因表达状态在肝脏再生的影响下是灵活的,而它们的代谢状态是稳健的。这一发现有助于阐明衰老与肝脏再生之间的关系,并确定肝脏疾病发病率随年龄增长的基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Differential Effects of Liver Regeneration on Aging-Related Changes in Gene Expression and Metabolic Function.

Aging causes significant changes in gene expression and metabolic function of cells in various organs. Although it is known that liver regeneration is delayed by aging, the effects of aging on changes in gene expression and metabolic functions in liver regeneration need further investigation. In this study, we comprehensively analyzed changes in gene expression and metabolic function by liver regeneration in young and old mice to examine the effects of aging on these changes. During the process of liver regeneration, the gene expression profiles of hepatocytes from young and old mice changed significantly in a stepwise manner while each remained close together. After the completion of liver regeneration, the genes with aging-specific expression patterns in old mouse hepatocytes changed to expression levels close to those in young mouse hepatocytes. In contrast to the results of these transcriptome analyses, the aging-specific changes in metabolic state detected in old mouse livers were found to be largely maintained after the completion of liver regeneration. These results demonstrated that the gene expression state in the liver of old mice is flexibly altered by liver regeneration, whereas their metabolic state is robust. This finding helps to elucidate the relationship between aging and liver regeneration and to determine the basis of the increased incidence of liver disease with aging.

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来源期刊
Aging Cell
Aging Cell Biochemistry, Genetics and Molecular Biology-Cell Biology
自引率
2.60%
发文量
212
期刊介绍: Aging Cell is an Open Access journal that focuses on the core aspects of the biology of aging, encompassing the entire spectrum of geroscience. The journal's content is dedicated to publishing research that uncovers the mechanisms behind the aging process and explores the connections between aging and various age-related diseases. This journal aims to provide a comprehensive understanding of the biological underpinnings of aging and its implications for human health. The journal is widely recognized and its content is abstracted and indexed by numerous databases and services, which facilitates its accessibility and impact in the scientific community. These include: Academic Search (EBSCO Publishing) Academic Search Alumni Edition (EBSCO Publishing) Academic Search Premier (EBSCO Publishing) Biological Science Database (ProQuest) CAS: Chemical Abstracts Service (ACS) Embase (Elsevier) InfoTrac (GALE Cengage) Ingenta Select ISI Alerting Services Journal Citation Reports/Science Edition (Clarivate Analytics) MEDLINE/PubMed (NLM) Natural Science Collection (ProQuest) PubMed Dietary Supplement Subset (NLM) Science Citation Index Expanded (Clarivate Analytics) SciTech Premium Collection (ProQuest) Web of Science (Clarivate Analytics) Being indexed in these databases ensures that the research published in Aging Cell is discoverable by researchers, clinicians, and other professionals interested in the field of aging and its associated health issues. This broad coverage helps to disseminate the journal's findings and contributes to the advancement of knowledge in geroscience.
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