NDUFA9 and its crotonylation modification promote browning of white adipocytes by activating mitochondrial function in mice

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Yuexia Liu, Zunhai Liu, Zeyu Ren, Qiannan Han, Xinhao Chen, Jialu Han, Guiping Qiu, Chao Sun
{"title":"NDUFA9 and its crotonylation modification promote browning of white adipocytes by activating mitochondrial function in mice","authors":"Yuexia Liu,&nbsp;Zunhai Liu,&nbsp;Zeyu Ren,&nbsp;Qiannan Han,&nbsp;Xinhao Chen,&nbsp;Jialu Han,&nbsp;Guiping Qiu,&nbsp;Chao Sun","doi":"10.1016/j.biocel.2024.106583","DOIUrl":null,"url":null,"abstract":"<div><p>Protein crotonylation plays a role in regulating cellular metabolism, gene expression, and other biological processes. NDUFA9 (NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 9) is closely associated with the activity and function of mitochondrial respiratory chain complex I. Mitochondrial function and respiratory chain are closely related to browning of white adipocytes, it’s speculated that NDUFA9 and its crotonylation are associated with browning of white adipocytes. Firstly, the effect of NDUFA9 on white adipose tissue was verified in white fat browning model mice, and it was found that NDUFA9 promoted mitochondrial respiration, thermogenesis, and browning of white adipose tissue. Secondly, in cellular studies, it was discovered that NDUFA9 facilitated browning of white adipocytes by enhancing mitochondrial function, mitochondrial complex I activity, ATP synthesis, and mitochondrial respiration. Again, the level of NDUFA9 crotonylation was increased by treating cells with vorinostat (SAHA)+sodium crotonate (NaCr) and overexpressing NDUFA9, it was found that NDUFA9 crotonylation promoted browning of white adipocytes. Meanwhile, the acetylation level of NDUFA9 was increased by treating cells with SAHA+sodium acetate (NaAc) and overexpressing NDUFA9, the assay revealed that NDUFA9 acetylation inhibited white adipocytes browning. Finally, combined with the competitive relationship between acetylation and crotonylation, it was also demonstrated that NDUFA9 crotonylation promoted browning of white adipocytes. Above results indicate that NDUFA9 and its crotonylation modification promote mitochondrial function, which in turn promotes browning of white adipocytes. This study establishes a theoretical foundation for the management and intervention of obesity, which is crucial in addressing obesity and related medical conditions in the future.</p></div>","PeriodicalId":3,"journal":{"name":"ACS Applied Electronic Materials","volume":null,"pages":null},"PeriodicalIF":4.3000,"publicationDate":"2024-04-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Electronic Materials","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1357272524000748","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, ELECTRICAL & ELECTRONIC","Score":null,"Total":0}
引用次数: 0

Abstract

Protein crotonylation plays a role in regulating cellular metabolism, gene expression, and other biological processes. NDUFA9 (NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 9) is closely associated with the activity and function of mitochondrial respiratory chain complex I. Mitochondrial function and respiratory chain are closely related to browning of white adipocytes, it’s speculated that NDUFA9 and its crotonylation are associated with browning of white adipocytes. Firstly, the effect of NDUFA9 on white adipose tissue was verified in white fat browning model mice, and it was found that NDUFA9 promoted mitochondrial respiration, thermogenesis, and browning of white adipose tissue. Secondly, in cellular studies, it was discovered that NDUFA9 facilitated browning of white adipocytes by enhancing mitochondrial function, mitochondrial complex I activity, ATP synthesis, and mitochondrial respiration. Again, the level of NDUFA9 crotonylation was increased by treating cells with vorinostat (SAHA)+sodium crotonate (NaCr) and overexpressing NDUFA9, it was found that NDUFA9 crotonylation promoted browning of white adipocytes. Meanwhile, the acetylation level of NDUFA9 was increased by treating cells with SAHA+sodium acetate (NaAc) and overexpressing NDUFA9, the assay revealed that NDUFA9 acetylation inhibited white adipocytes browning. Finally, combined with the competitive relationship between acetylation and crotonylation, it was also demonstrated that NDUFA9 crotonylation promoted browning of white adipocytes. Above results indicate that NDUFA9 and its crotonylation modification promote mitochondrial function, which in turn promotes browning of white adipocytes. This study establishes a theoretical foundation for the management and intervention of obesity, which is crucial in addressing obesity and related medical conditions in the future.

NDUFA9 及其巴豆酰化修饰通过激活线粒体功能促进小鼠白色脂肪细胞褐变
蛋白质巴豆酰化在调节细胞代谢、基因表达和其他生物过程中发挥作用。NDUFA9(NADH脱氢酶[泛醌]1α亚复合物亚基9)与线粒体呼吸链复合物I的活性和功能密切相关,线粒体功能和呼吸链与白色脂肪细胞的褐变密切相关,因此推测NDUFA9及其巴豆酰化与白色脂肪细胞的褐变有关。首先,在白色脂肪褐变模型小鼠中验证了 NDUFA9 对白色脂肪组织的影响,发现 NDUFA9 促进线粒体呼吸、产热和白色脂肪组织的褐变。其次,在细胞研究中发现,NDUFA9 通过增强线粒体功能、线粒体复合物 I 活性、ATP 合成和线粒体呼吸,促进了白色脂肪细胞的棕色化。同样,用伏立诺他(SAHA)+巴豆酸钠(NaCr)处理细胞并过表达NDUFA9,提高NDUFA9巴豆酰化水平,发现NDUFA9巴豆酰化促进了白色脂肪细胞的褐变。同时,用SAHA+醋酸钠(NaAc)处理细胞并过表达NDUFA9,提高了NDUFA9的乙酰化水平,结果发现NDUFA9乙酰化抑制了白色脂肪细胞的褐变。最后,结合乙酰化和巴豆酰化之间的竞争关系,还证明了 NDUFA9 巴豆酰化促进了白色脂肪细胞的褐变。以上结果表明,NDUFA9及其巴豆酰化修饰可促进线粒体功能,进而促进白色脂肪细胞的褐变。这项研究为肥胖症的管理和干预奠定了理论基础,对今后解决肥胖症及相关疾病至关重要。
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
CiteScore
7.20
自引率
4.30%
发文量
567
×
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