Fenofibrate-promoted hepatomegaly and liver regeneration are PPARα-dependent and partially related to the YAP pathway

IF 14.7 1区 医学 Q1 PHARMACOLOGY & PHARMACY
Shicheng Fan , Yue Gao , Pengfei Zhao , Guomin Xie , Yanying Zhou , Xiao Yang , Xuan Li , Shuaishuai Zhang , Frank J. Gonzalez , Aijuan Qu , Min Huang , Huichang Bi
{"title":"Fenofibrate-promoted hepatomegaly and liver regeneration are PPARα-dependent and partially related to the YAP pathway","authors":"Shicheng Fan ,&nbsp;Yue Gao ,&nbsp;Pengfei Zhao ,&nbsp;Guomin Xie ,&nbsp;Yanying Zhou ,&nbsp;Xiao Yang ,&nbsp;Xuan Li ,&nbsp;Shuaishuai Zhang ,&nbsp;Frank J. Gonzalez ,&nbsp;Aijuan Qu ,&nbsp;Min Huang ,&nbsp;Huichang Bi","doi":"10.1016/j.apsb.2024.03.030","DOIUrl":null,"url":null,"abstract":"<div><p>Fenofibrate, a peroxisome proliferator-activated receptor <em>α</em> (PPAR<em>α</em>) agonist, is widely prescribed for hyperlipidemia management. Recent studies also showed that it has therapeutic potential in various liver diseases. However, its effects on hepatomegaly and liver regeneration and the involved mechanisms remain unclear. Here, the study showed that fenofibrate significantly promoted liver enlargement and regeneration post-partial hepatectomy in mice, which was dependent on hepatocyte-expressed PPAR<em>α</em>. Yes-associated protein (YAP) is pivotal in manipulating liver growth and regeneration. We further identified that fenofibrate activated YAP signaling by suppressing its K48-linked ubiquitination, promoting its K63-linked ubiquitination, and enhancing the interaction and transcriptional activity of the YAP–TEAD complex. Pharmacological inhibition of YAP–TEAD interaction using verteporfin or suppression of YAP using AAV <em>Yap</em> shRNA in mice significantly attenuated fenofibrate-induced hepatomegaly. Other factors, such as MYC, KRT23, RAS, and RHOA, might also participate in fenofibrate-promoted hepatomegaly and liver regeneration. These studies demonstrate that fenofibrate-promoted liver enlargement and regeneration are PPAR<em>α</em>-dependent and partially through activating the YAP signaling, with clinical implications of fenofibrate as a novel therapeutic agent for promoting liver regeneration.</p></div>","PeriodicalId":6906,"journal":{"name":"Acta Pharmaceutica Sinica. B","volume":null,"pages":null},"PeriodicalIF":14.7000,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2211383524001230/pdfft?md5=8545325dc4c312649e8b61f5a4085c9f&pid=1-s2.0-S2211383524001230-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta Pharmaceutica Sinica. B","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2211383524001230","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0

Abstract

Fenofibrate, a peroxisome proliferator-activated receptor α (PPARα) agonist, is widely prescribed for hyperlipidemia management. Recent studies also showed that it has therapeutic potential in various liver diseases. However, its effects on hepatomegaly and liver regeneration and the involved mechanisms remain unclear. Here, the study showed that fenofibrate significantly promoted liver enlargement and regeneration post-partial hepatectomy in mice, which was dependent on hepatocyte-expressed PPARα. Yes-associated protein (YAP) is pivotal in manipulating liver growth and regeneration. We further identified that fenofibrate activated YAP signaling by suppressing its K48-linked ubiquitination, promoting its K63-linked ubiquitination, and enhancing the interaction and transcriptional activity of the YAP–TEAD complex. Pharmacological inhibition of YAP–TEAD interaction using verteporfin or suppression of YAP using AAV Yap shRNA in mice significantly attenuated fenofibrate-induced hepatomegaly. Other factors, such as MYC, KRT23, RAS, and RHOA, might also participate in fenofibrate-promoted hepatomegaly and liver regeneration. These studies demonstrate that fenofibrate-promoted liver enlargement and regeneration are PPARα-dependent and partially through activating the YAP signaling, with clinical implications of fenofibrate as a novel therapeutic agent for promoting liver regeneration.

Abstract Image

Abstract Image

非诺贝特促进的肝肿大和肝再生是 PPARα 依赖性的,并与 YAP 通路部分相关
非诺贝特是一种过氧化物酶体增殖激活受体α(PPARα)激动剂,被广泛用于治疗高脂血症。最近的研究也表明,它对各种肝病也有治疗潜力。然而,它对肝肿大和肝脏再生的影响及其机制仍不清楚。本研究表明,非诺贝特能显著促进小鼠肝脏的增大和肝切除后的再生,而这取决于肝细胞表达的PPARα。是相关蛋白(YAP)在操纵肝脏生长和再生方面起着关键作用。我们进一步发现,非诺贝特通过抑制其与 K48 链接的泛素化、促进其与 K63 链接的泛素化以及增强 YAP-TEAD 复合物的相互作用和转录活性来激活 YAP 信号转导。使用维替泊芬(verteporfin)对YAP-TEAD相互作用进行药理抑制,或使用AAV Yap shRNA对小鼠的YAP进行抑制,可显著减轻非诺贝特诱导的肝肿大。其他因素,如 MYC、KRT23、RAS 和 RHOA,也可能参与非诺贝特促进的肝肿大和肝脏再生。这些研究表明,非诺贝特促进肝脏肿大和再生是PPARα依赖性的,部分是通过激活YAP信号转导实现的,非诺贝特作为促进肝脏再生的新型治疗药物具有临床意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Acta Pharmaceutica Sinica. B
Acta Pharmaceutica Sinica. B Pharmacology, Toxicology and Pharmaceutics-General Pharmacology, Toxicology and Pharmaceutics
CiteScore
22.40
自引率
5.50%
发文量
1051
审稿时长
19 weeks
期刊介绍: The Journal of the Institute of Materia Medica, Chinese Academy of Medical Sciences, and the Chinese Pharmaceutical Association oversees the peer review process for Acta Pharmaceutica Sinica. B (APSB). Published monthly in English, APSB is dedicated to disseminating significant original research articles, rapid communications, and high-quality reviews that highlight recent advances across various pharmaceutical sciences domains. These encompass pharmacology, pharmaceutics, medicinal chemistry, natural products, pharmacognosy, pharmaceutical analysis, and pharmacokinetics. A part of the Acta Pharmaceutica Sinica series, established in 1953 and indexed in prominent databases like Chemical Abstracts, Index Medicus, SciFinder Scholar, Biological Abstracts, International Pharmaceutical Abstracts, Cambridge Scientific Abstracts, and Current Bibliography on Science and Technology, APSB is sponsored by the Institute of Materia Medica, Chinese Academy of Medical Sciences, and the Chinese Pharmaceutical Association. Its production and hosting are facilitated by Elsevier B.V. This collaborative effort ensures APSB's commitment to delivering valuable contributions to the pharmaceutical sciences community.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信