• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

YAP和TAZ:代谢与细胞重编程交叉路口的介质

YAP and TAZ Mediators at the Crossroad between Metabolic and Cellular Reprogramming.

作者信息

Di Benedetto Giorgia, Parisi Silvia, Russo Tommaso, Passaro Fabiana

机构信息

Department of Molecular Medicine and Medical Biotechnology, University of Naples Federico II, 40, 80138 Napoli, Italy.

出版信息

Metabolites. 2021 Mar 8;11(3):154. doi: 10.3390/metabo11030154.

DOI:10.3390/metabo11030154
PMID:33800464
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7999074/
Abstract

Cell reprogramming can either refer to a direct conversion of a specialized cell into another or to a reversal of a somatic cell into an induced pluripotent stem cell (iPSC). It implies a peculiar modification of the epigenetic asset and gene regulatory networks needed for a new cell, to better fit the new phenotype of the incoming cell type. Cellular reprogramming also implies a metabolic rearrangement, similar to that observed upon tumorigenesis, with a transition from oxidative phosphorylation to aerobic glycolysis. The induction of a reprogramming process requires a nexus of signaling pathways, mixing a range of local and systemic information, and accumulating evidence points to the crucial role exerted by the Hippo pathway components Yes-Associated Protein (YAP) and Transcriptional Co-activator with PDZ-binding Motif (TAZ). In this review, we will first provide a synopsis of the Hippo pathway and its function during reprogramming and tissue regeneration, then we introduce the latest knowledge on the interplay between YAP/TAZ and metabolism and, finally, we discuss the possible role of YAP/TAZ in the orchestration of the metabolic switch upon cellular reprogramming.

摘要

细胞重编程既可以指将一种特化细胞直接转化为另一种细胞,也可以指将体细胞逆转为诱导多能干细胞(iPSC)。这意味着对新细胞所需的表观遗传特征和基因调控网络进行特殊修饰,以更好地适应新进入细胞类型的新表型。细胞重编程还意味着代谢重排,类似于在肿瘤发生过程中观察到的情况,即从氧化磷酸化转变为有氧糖酵解。重编程过程的诱导需要一系列信号通路的关联,整合一系列局部和全身信息,并且越来越多的证据表明,Hippo信号通路的组成部分Yes相关蛋白(YAP)和含PDZ结合基序的转录共激活因子(TAZ)发挥着关键作用。在这篇综述中,我们首先将概述Hippo信号通路及其在重编程和组织再生过程中的功能,然后介绍关于YAP/TAZ与代谢之间相互作用的最新知识,最后讨论YAP/TAZ在细胞重编程过程中协调代谢转换的可能作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/941f/7999074/a506d28af1b2/metabolites-11-00154-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/941f/7999074/130c39fb3310/metabolites-11-00154-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/941f/7999074/902f5e7d18bf/metabolites-11-00154-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/941f/7999074/a506d28af1b2/metabolites-11-00154-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/941f/7999074/130c39fb3310/metabolites-11-00154-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/941f/7999074/902f5e7d18bf/metabolites-11-00154-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/941f/7999074/a506d28af1b2/metabolites-11-00154-g003.jpg

相似文献

1
YAP and TAZ Mediators at the Crossroad between Metabolic and Cellular Reprogramming.YAP和TAZ:代谢与细胞重编程交叉路口的介质
Metabolites. 2021 Mar 8;11(3):154. doi: 10.3390/metabo11030154.
2
A Potential Role of YAP/TAZ in the Interplay Between Metastasis and Metabolic Alterations.YAP/TAZ在转移与代谢改变相互作用中的潜在作用
Front Oncol. 2020 Jun 11;10:928. doi: 10.3389/fonc.2020.00928. eCollection 2020.
3
Targeting the Hippo Signaling Pathway for Tissue Regeneration and Cancer Therapy.靶向 Hippo 信号通路进行组织再生和癌症治疗。
Genes (Basel). 2016 Aug 30;7(9):55. doi: 10.3390/genes7090055.
4
The Hippo-YAP/TAZ Signaling Pathway in Intestinal Self-Renewal and Regeneration After Injury.损伤后肠道自我更新与再生中的 Hippo-YAP/TAZ 信号通路
Front Cell Dev Biol. 2022 Jul 19;10:894737. doi: 10.3389/fcell.2022.894737. eCollection 2022.
5
The role of YAP/TAZ activity in cancer metabolic reprogramming.YAP/TAZ 活性在癌症代谢重编程中的作用。
Mol Cancer. 2018 Sep 3;17(1):134. doi: 10.1186/s12943-018-0882-1.
6
Cysteine S-Glutathionylation Promotes Stability and Activation of the Hippo Downstream Effector Transcriptional Co-activator with PDZ-binding Motif (TAZ).半胱氨酸S-谷胱甘肽化促进具有PDZ结合基序的Hippo下游效应转录共激活因子(TAZ)的稳定性和激活。
J Biol Chem. 2016 May 27;291(22):11596-607. doi: 10.1074/jbc.M115.712539. Epub 2016 Apr 5.
7
Yes-associated protein (YAP) and transcriptional coactivator with a PDZ-binding motif (TAZ): a nexus between hypoxia and cancer.Yes相关蛋白(YAP)和含PDZ结合基序的转录共激活因子(TAZ):缺氧与癌症之间的联系
Acta Pharm Sin B. 2020 Jun;10(6):947-960. doi: 10.1016/j.apsb.2019.12.010. Epub 2019 Dec 19.
8
miR-582-5p Is a Tumor Suppressor microRNA Targeting the Hippo-YAP/TAZ Signaling Pathway in Non-Small Cell Lung Cancer.miR-582-5p是一种靶向非小细胞肺癌中Hippo-YAP/TAZ信号通路的肿瘤抑制性微小RNA。
Cancers (Basel). 2021 Feb 11;13(4):756. doi: 10.3390/cancers13040756.
9
Suppression of YAP/TAZ-Notch1-NICD axis by bromodomain and extraterminal protein inhibition impairs liver regeneration.通过抑制溴结构域和额外末端蛋白来抑制YAP/TAZ-Notch1-NICD轴会损害肝脏再生。
Theranostics. 2019 May 31;9(13):3840-3852. doi: 10.7150/thno.33370. eCollection 2019.
10
WW Domain-Containing Proteins YAP and TAZ in the Hippo Pathway as Key Regulators in Stemness Maintenance, Tissue Homeostasis, and Tumorigenesis.河马通路中含WW结构域的蛋白质YAP和TAZ作为干细胞干性维持、组织稳态和肿瘤发生的关键调节因子
Front Oncol. 2019 Feb 11;9:60. doi: 10.3389/fonc.2019.00060. eCollection 2019.

引用本文的文献

1
WIPF1 regulates stemness in small cell lung cancer.WIPF1调节小细胞肺癌中的干性。
Sci Prog. 2025 Apr-Jun;108(2):368504251345012. doi: 10.1177/00368504251345012. Epub 2025 May 25.
2
Targeting the Hippo/YAP1 signaling pathway in hepatocellular carcinoma: From mechanisms to therapeutic drugs (Review).靶向肝细胞癌中的 Hippo/YAP1 信号通路:从机制到治疗药物(综述)。
Int J Oncol. 2024 Sep;65(3). doi: 10.3892/ijo.2024.5676. Epub 2024 Aug 2.
3
Acoustic vibration promotes in vitro expansion of human embryonic stem cells.声学振动促进人胚胎干细胞的体外扩增。

本文引用的文献

1
Nuclear organization and regulation of the differentiated state.核组织与分化状态的调控。
Cell Mol Life Sci. 2021 Apr;78(7):3141-3158. doi: 10.1007/s00018-020-03731-4. Epub 2021 Jan 28.
2
Identification of RNA-binding proteins that partner with Lin28a to regulate Dnmt3a expression.鉴定与 Lin28a 相互作用的 RNA 结合蛋白,以调节 Dnmt3a 的表达。
Sci Rep. 2021 Jan 27;11(1):2345. doi: 10.1038/s41598-021-81429-8.
3
YAP contributes to DNA methylation remodeling upon mouse embryonic stem cell differentiation.YAP 有助于小鼠胚胎干细胞分化时的 DNA 甲基化重塑。
Am J Stem Cells. 2024 Jun 15;13(3):143-151. doi: 10.62347/PJFC2708. eCollection 2024.
4
Lung injury-induced activated endothelial cell states persist in aging-associated progressive fibrosis.肺损伤诱导的激活的内皮细胞状态在与年龄相关的进行性纤维化中持续存在。
Nat Commun. 2024 Jun 27;15(1):5449. doi: 10.1038/s41467-024-49545-x.
5
Avian iPSC Derivation to Recover Threatened Wild Species: A Comprehensive Review in Light of Well-Established Protocols.利用鸟类诱导多能干细胞衍生技术拯救濒危野生物种:基于成熟方案的综合综述
Animals (Basel). 2024 Jan 10;14(2):220. doi: 10.3390/ani14020220.
6
Yap/Taz activity is associated with increased expression of phosphoglycerate dehydrogenase that supports myoblast proliferation.Yap/Taz 的活性与磷酸甘油酸脱氢酶的表达增加有关,后者支持成肌细胞的增殖。
Cell Tissue Res. 2024 Mar;395(3):271-283. doi: 10.1007/s00441-023-03851-w. Epub 2024 Jan 6.
7
Hippo/YAP signaling pathway: a new therapeutic target for diabetes mellitus and vascular complications.河马/Yes相关蛋白信号通路:糖尿病及血管并发症的新治疗靶点。
Ther Adv Endocrinol Metab. 2023 Dec 25;14:20420188231220134. doi: 10.1177/20420188231220134. eCollection 2023.
8
FN1 mediated activation of aspartate metabolism promotes the progression of triple-negative and luminal a breast cancer.FN1 介导的天冬氨酸代谢激活促进三阴性和腔 A 型乳腺癌的进展。
Breast Cancer Res Treat. 2023 Oct;201(3):515-533. doi: 10.1007/s10549-023-07032-9. Epub 2023 Jul 17.
9
Cross-lineage potential of Ascl1 uncovered by comparing diverse reprogramming regulatomes.通过比较不同的重编程调控组,揭示了 Ascl1 的跨谱系潜力。
Cell Stem Cell. 2022 Oct 6;29(10):1491-1504.e9. doi: 10.1016/j.stem.2022.09.006.
10
YAP: The nexus between metabolism and cardiac remodeling.YAP:代谢与心脏重构之间的联系。
J Clin Invest. 2022 Mar 15;132(6). doi: 10.1172/JCI157664.
J Biol Chem. 2021 Jan-Jun;296:100138. doi: 10.1074/jbc.RA120.015896. Epub 2020 Dec 6.
4
The Key Role of MicroRNAs in Self-Renewal and Differentiation of Embryonic Stem Cells.微小 RNA 在胚胎干细胞自我更新和分化中的关键作用。
Int J Mol Sci. 2020 Aug 31;21(17):6285. doi: 10.3390/ijms21176285.
5
Soft Matrix Promotes Cardiac Reprogramming via Inhibition of YAP/TAZ and Suppression of Fibroblast Signatures.软基质通过抑制YAP/TAZ和抑制成纤维细胞特征促进心脏重编程。
Stem Cell Reports. 2020 Sep 8;15(3):612-628. doi: 10.1016/j.stemcr.2020.07.022. Epub 2020 Aug 27.
6
Epithelial-Mesenchymal Transition and Metabolic Switching in Cancer: Lessons From Somatic Cell Reprogramming.癌症中的上皮-间质转化与代谢转换:来自体细胞重编程的启示
Front Cell Dev Biol. 2020 Aug 6;8:760. doi: 10.3389/fcell.2020.00760. eCollection 2020.
7
Role of YAP/TAZ in Cell Lineage Fate Determination and Related Signaling Pathways.YAP/TAZ在细胞谱系命运决定及相关信号通路中的作用
Front Cell Dev Biol. 2020 Jul 30;8:735. doi: 10.3389/fcell.2020.00735. eCollection 2020.
8
A Potential Role of YAP/TAZ in the Interplay Between Metastasis and Metabolic Alterations.YAP/TAZ在转移与代谢改变相互作用中的潜在作用
Front Oncol. 2020 Jun 11;10:928. doi: 10.3389/fonc.2020.00928. eCollection 2020.
9
Bmi1 inhibitor PTC-209 promotes Chemically-induced Direct Cardiac Reprogramming of cardiac fibroblasts into cardiomyocytes.Bmi1 抑制剂 PTC-209 促进化学诱导的心脏成纤维细胞向心肌细胞的直接重编程。
Sci Rep. 2020 Apr 28;10(1):7129. doi: 10.1038/s41598-020-63992-8.
10
YAP Non-cell-autonomously Promotes Pluripotency Induction in Mouse Cells.YAP 非细胞自主促进小鼠细胞的多能性诱导。
Stem Cell Reports. 2020 Apr 14;14(4):730-743. doi: 10.1016/j.stemcr.2020.03.006. Epub 2020 Apr 2.