The browning and mobilization of subcutaneous white adipose tissue supports efficient skin repair

IF 27.7 1区 生物学 Q1 CELL BIOLOGY Cell metabolism Pub Date : 2024-06-04 DOI:10.1016/j.cmet.2024.05.005
Junrong Cai, Yuping Quan, Shaowei Zhu, , Qian Zhang, Juzi Liu, Zhuokai Liang, Yunjun Liao, Wenqing Jiang, Yufei He, Ting Su, Feng Lu
{"title":"The browning and mobilization of subcutaneous white adipose tissue supports efficient skin repair","authors":"Junrong Cai, Yuping Quan, Shaowei Zhu, , Qian Zhang, Juzi Liu, Zhuokai Liang, Yunjun Liao, Wenqing Jiang, Yufei He, Ting Su, Feng Lu","doi":"10.1016/j.cmet.2024.05.005","DOIUrl":null,"url":null,"abstract":"<p>Adipocytes in dermis are considered to be important participants in skin repair and regeneration, but the role of subcutaneous white adipose tissue (sWAT) in skin repair is poorly understood. Here, we revealed the dynamic changes of sWAT during wound healing process. Lineage-tracing mouse studies revealed that sWAT would enter into the large wound bed and participate in the formation of granulation tissue. Moreover, sWAT undergoes beiging after skin injury. Inhibition of sWAT beiging by genetically silencing PRDM16, a key regulator to beiging, hindered wound healing process. The transcriptomics results suggested that beige adipocytes in sWAT abundantly express neuregulin 4 (NRG4), which regulated macrophage polarization and the function of myofibroblasts. In diabetic wounds, the beiging of sWAT was significantly suppressed. Thus, adipocytes from sWAT regulate multiple aspects of repair and may be therapeutic for inflammatory diseases and defective wound healing associated with aging and diabetes.</p>","PeriodicalId":9840,"journal":{"name":"Cell metabolism","volume":"100 1","pages":""},"PeriodicalIF":27.7000,"publicationDate":"2024-06-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cell metabolism","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/j.cmet.2024.05.005","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Adipocytes in dermis are considered to be important participants in skin repair and regeneration, but the role of subcutaneous white adipose tissue (sWAT) in skin repair is poorly understood. Here, we revealed the dynamic changes of sWAT during wound healing process. Lineage-tracing mouse studies revealed that sWAT would enter into the large wound bed and participate in the formation of granulation tissue. Moreover, sWAT undergoes beiging after skin injury. Inhibition of sWAT beiging by genetically silencing PRDM16, a key regulator to beiging, hindered wound healing process. The transcriptomics results suggested that beige adipocytes in sWAT abundantly express neuregulin 4 (NRG4), which regulated macrophage polarization and the function of myofibroblasts. In diabetic wounds, the beiging of sWAT was significantly suppressed. Thus, adipocytes from sWAT regulate multiple aspects of repair and may be therapeutic for inflammatory diseases and defective wound healing associated with aging and diabetes.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
皮下白色脂肪组织的褐变和动员有助于有效修复皮肤
真皮中的脂肪细胞被认为是皮肤修复和再生的重要参与者,但人们对皮下白色脂肪组织(sWAT)在皮肤修复中的作用却知之甚少。在这里,我们揭示了皮下白色脂肪组织在伤口愈合过程中的动态变化。线性追踪小鼠研究发现,sWAT 会进入大面积伤口床并参与肉芽组织的形成。此外,皮肤损伤后,sWAT 会发生豆状化。通过基因沉默PRDM16来抑制sWAT豆状化,PRDM16是豆状化的关键调节因子,它阻碍了伤口愈合过程。转录组学结果表明,sWAT中的米色脂肪细胞大量表达神经胶质蛋白4(NRG4),而NRG4能调节巨噬细胞的极化和肌成纤维细胞的功能。在糖尿病伤口中,sWAT 的米色化明显受到抑制。因此,sWAT 的脂肪细胞可调控修复的多个方面,可治疗与衰老和糖尿病相关的炎症性疾病和伤口愈合缺陷。
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 去求助
来源期刊
Cell metabolism
Cell metabolism 生物-内分泌学与代谢
CiteScore
48.60
自引率
1.40%
发文量
173
审稿时长
2.5 months
期刊介绍: Cell Metabolism is a top research journal established in 2005 that focuses on publishing original and impactful papers in the field of metabolic research.It covers a wide range of topics including diabetes, obesity, cardiovascular biology, aging and stress responses, circadian biology, and many others. Cell Metabolism aims to contribute to the advancement of metabolic research by providing a platform for the publication and dissemination of high-quality research and thought-provoking articles.
期刊最新文献
Acute and circadian feedforward regulation of agouti-related peptide hunger neurons A famsin-glucagon axis mediates glucose homeostasis Early downmodulation of tumor glycolysis predicts response to fasting-mimicking diet in triple-negative breast cancer patients Unveiling adipose populations linked to metabolic health in obesity FcRn-dependent IgG accumulation in adipose tissue unmasks obesity pathophysiology
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1