科研成果详情

题名Investigation of Metabolic and Inflammatory Disorder in the Aging FGF21 Knockout Mouse
作者
发表日期2024-04-24
发表期刊INFLAMMATION   影响因子和分区
语种英语
原始文献类型Article ; Early Access
关键词aging fibroblast growth factor 21 inflammatory response fatty liver transcriptomics metabolomics and lipidomics
其他关键词LYSOPHOSPHATIDYLCHOLINE ; IDENTIFICATION ; ACID
摘要Aging is a physiological condition accomplished with persistent low-grade inflammation and metabolic disorders. FGF21 has been reported to act as a potent longevity determinant, involving inflammatory response and energy metabolism. In this study, we engineered aging FGF21 knockout mice of 36-40 weeks and observed that FGF21 deficiency manifests a spontaneous inflammatory response of lung and abnormal accumulation of lipids in liver. On one hand, inflamed state in lungs and increased circulating inflammatory cytokines were found in FGF21 knockout mice of 36-40 weeks. To evaluate the ability of FGF21 to suppress inflammation, a subsequent study found that FGF21 knockout aggravated LPS-induced pulmonary exudation and inflammatory infiltration in mice, while exogenous administration of FGF21 reversed these malignant phenotypes by enhancing microvascular endothelial junction. On the other hand, FGF21 knockout induces fatty liver in aging mice, characterized by excessive accumulation of triglycerides within hepatocytes. Further quantitative metabolomics and lipidomics analysis revealed perturbed metabolic profile in liver lacking FGF21, including disrupted glucose and lipids metabolism, glycerophospholipid metabolism, and amino acid metabolism. Taken together, this investigation reveals the protective role of FGF21 during aging by weakening the inflammatory response and balancing energy metabolism.
资助项目Key scientific research project of Wenzhou[2020ZY0036];Science and Technology Innovation Activity Plan for College Students of Zhejiang Province[2022R413A040];
出版者SPRINGER/PLENUM PUBLISHERS
ISSN0360-3997
EISSN1573-2576
DOI10.1007/s10753-024-02032-3
页数23
WOS类目Cell Biology ; Immunology
WOS研究方向Cell Biology ; Immunology
WOS记录号WOS:001207102100001
收录类别SCIE ; SCOPUS ; PUBMED
在线发表日期2024-04
URL查看原文
PubMed ID38653921
SCOPUSEID2-s2.0-85191091960
通讯作者地址[Huang, Xiao-Ying]Division of Pulmonary Medicine,the First Affiliated Hospital,Wenzhou Medical University,Wenzhou Key Laboratory of Interdiscipline and Translational Medicine,Wenzhou Key Laboratory of Heart and Lung,Zhejiang,Wenzhou,325000,China
Scopus学科分类Immunology and Allergy;Immunology
引用统计
文献类型期刊论文
条目标识符https://kms.wmu.edu.cn/handle/3ETUA0LF/212549
专题附属第一医院
药学院(分析测试中心)
第一临床医学院(信息与工程学院)、附属第一医院_硕士
通讯作者Huang, Xiao-Ying
作者单位
1.Division of Pulmonary Medicine,the First Affiliated Hospital,Wenzhou Medical University,Wenzhou Key Laboratory of Interdiscipline and Translational Medicine,Wenzhou Key Laboratory of Heart and Lung,Zhejiang,Wenzhou,325000,China;
2.School of Pharmacy,Wenzhou Medical University,Chashan University Park, Zhejiang,Wenzhou,325000,China
第一作者单位附属第一医院
通讯作者单位附属第一医院
第一作者的第一单位附属第一医院
推荐引用方式
GB/T 7714
Cai, Lu-Qiong,Li, Xiu-Chun,Wang, Yang-Yue,et al. Investigation of Metabolic and Inflammatory Disorder in the Aging FGF21 Knockout Mouse[J]. INFLAMMATION,2024.
APA Cai, Lu-Qiong., Li, Xiu-Chun., Wang, Yang-Yue., Chen, Yu-Xin., Zhu, Xia-Yan., ... & Huang, Xiao-Ying. (2024). Investigation of Metabolic and Inflammatory Disorder in the Aging FGF21 Knockout Mouse. INFLAMMATION.
MLA Cai, Lu-Qiong,et al."Investigation of Metabolic and Inflammatory Disorder in the Aging FGF21 Knockout Mouse".INFLAMMATION (2024).

条目包含的文件

条目无相关文件。
个性服务
查看访问统计
谷歌学术
谷歌学术中相似的文章
[Cai, Lu-Qiong]的文章
[Li, Xiu-Chun]的文章
[Wang, Yang-Yue]的文章
百度学术
百度学术中相似的文章
[Cai, Lu-Qiong]的文章
[Li, Xiu-Chun]的文章
[Wang, Yang-Yue]的文章
必应学术
必应学术中相似的文章
[Cai, Lu-Qiong]的文章
[Li, Xiu-Chun]的文章
[Wang, Yang-Yue]的文章
相关权益政策
暂无数据
收藏/分享
所有评论 (0)
暂无评论
 

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。