• 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

Nur77 基因敲除导致斑马鱼发生氨基酸、脂类和葡萄糖代谢紊乱

Knockout of Nur77 Leads to Amino Acid, Lipid, and Glucose Metabolism Disorders in Zebrafish.

机构信息

Fujian Provincial Key Laboratory of Innovative Drug Target Research, School of Pharmaceutical Sciences, Xiamen University, Xiamen, China.

State Key Laboratory of Cellular Stress Biology, School of Life Sciences, Xiamen University, Xiamen, China.

出版信息

Front Endocrinol (Lausanne). 2022 Apr 25;13:864631. doi: 10.3389/fendo.2022.864631. eCollection 2022.

DOI:10.3389/fendo.2022.864631
PMID:35547009
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9084189/
Abstract

Orphan nuclear receptor Nur77 has been reported to be implicated in a diverse range of metabolic processes, including carbohydrate metabolism and lipid metabolism. However, the detailed mechanism of Nur77 in the regulation of metabolic pathway still needs to be further investigated. In this study, we created a global knockout zebrafish model by CRISPR/Cas9 technique, and then performed whole-organism RNA sequencing analysis in wildtype and -deficient zebrafish to dissect the genetic changes in metabolic-related pathways. We found that many genes involved in amino acid, lipid, and carbohydrate metabolism changed by more than twofold. Furthermore, we revealed that mutant displayed increased total cholesterol (TC) and triglyceride (TG), alteration in total amino acids, as well as elevated glucose. We also demonstrated that the elevated glucose was not due to the change of glucose uptake but was likely caused by the disorder of glycolysis/gluconeogenesis and the impaired β-cell function, including downregulated expression, reduced β-cell mass, and suppressed insulin secretion. Importantly, we also verified that targeted expression of Nur77 in the β cells is sufficient to rescue the β-cell defects in global larvae zebrafish. These results provide new information about the global metabolic network that Nur77 signaling regulates, as well as the role of Nur77 in β-cell function.

摘要

孤儿核受体 Nur77 被报道参与多种代谢过程,包括碳水化合物代谢和脂质代谢。然而,Nur77 在调节代谢途径中的详细机制仍需要进一步研究。在这项研究中,我们使用 CRISPR/Cas9 技术创建了一个全局缺失的斑马鱼模型,然后对野生型和 -/- 斑马鱼进行全器官 RNA 测序分析,以剖析代谢相关途径中的遗传变化。我们发现许多参与氨基酸、脂质和碳水化合物代谢的基因发生了两倍以上的变化。此外,我们揭示了 -/- 突变体显示总胆固醇 (TC) 和甘油三酯 (TG) 升高、总氨基酸改变以及葡萄糖升高。我们还表明,葡萄糖升高不是由于葡萄糖摄取的变化,而是可能由于糖酵解/糖异生的紊乱和β细胞功能受损引起的,包括下调的表达、β细胞质量减少和胰岛素分泌抑制。重要的是,我们还验证了 Nur77 在β细胞中的靶向表达足以挽救全局缺失的斑马鱼幼虫中的β细胞缺陷。这些结果提供了关于 Nur77 信号调节的全局代谢网络以及 Nur77 在β细胞功能中的作用的新信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b74/9084189/654e1cafe98b/fendo-13-864631-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b74/9084189/802655e7581d/fendo-13-864631-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b74/9084189/980658c27c9b/fendo-13-864631-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b74/9084189/f1447135d77b/fendo-13-864631-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b74/9084189/665f35914a25/fendo-13-864631-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b74/9084189/5720f5fac9d1/fendo-13-864631-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b74/9084189/cb38093f3ea8/fendo-13-864631-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b74/9084189/654e1cafe98b/fendo-13-864631-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b74/9084189/802655e7581d/fendo-13-864631-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b74/9084189/980658c27c9b/fendo-13-864631-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b74/9084189/f1447135d77b/fendo-13-864631-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b74/9084189/665f35914a25/fendo-13-864631-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b74/9084189/5720f5fac9d1/fendo-13-864631-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b74/9084189/cb38093f3ea8/fendo-13-864631-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b74/9084189/654e1cafe98b/fendo-13-864631-g007.jpg

相似文献

1
Knockout of Nur77 Leads to Amino Acid, Lipid, and Glucose Metabolism Disorders in Zebrafish.Nur77 基因敲除导致斑马鱼发生氨基酸、脂类和葡萄糖代谢紊乱
Front Endocrinol (Lausanne). 2022 Apr 25;13:864631. doi: 10.3389/fendo.2022.864631. eCollection 2022.
2
Insulin resistance and altered systemic glucose metabolism in mice lacking Nur77.缺乏Nur77的小鼠中的胰岛素抵抗和全身性葡萄糖代谢改变。
Diabetes. 2009 Dec;58(12):2788-96. doi: 10.2337/db09-0763. Epub 2009 Sep 9.
3
Nur77 regulates lipolysis in skeletal muscle cells. Evidence for cross-talk between the beta-adrenergic and an orphan nuclear hormone receptor pathway.Nur77调节骨骼肌细胞中的脂肪分解。β-肾上腺素能和孤儿核激素受体途径之间存在相互作用的证据。
J Biol Chem. 2005 Apr 1;280(13):12573-84. doi: 10.1074/jbc.M409580200. Epub 2005 Jan 6.
4
Role of phosphoenolpyruvate carboxykinase 1 (pck1) in mediating nutrient metabolism in zebrafish.磷酸烯醇式丙酮酸羧激酶1(pck1)在介导斑马鱼营养代谢中的作用。
Funct Integr Genomics. 2023 Feb 25;23(1):67. doi: 10.1007/s10142-023-00993-6.
5
Global Transcriptomic Analysis of Zebrafish Glucagon Receptor Mutant Reveals Its Regulated Metabolic Network.斑马鱼胰高血糖素受体突变体的全转录组分析揭示了其调控的代谢网络。
Int J Mol Sci. 2020 Jan 22;21(3):724. doi: 10.3390/ijms21030724.
6
Overexpression of the orphan receptor Nur77 alters glucose metabolism in rat muscle cells and rat muscle in vivo.孤儿受体 Nur77 的过表达改变了大鼠肌肉细胞和体内大鼠肌肉的糖代谢。
Diabetologia. 2010 Jun;53(6):1174-83. doi: 10.1007/s00125-010-1703-2. Epub 2010 Mar 9.
7
The nuclear orphan receptor Nur77 is a lipotoxicity sensor regulating glucose-induced insulin secretion in pancreatic β-cells.核孤儿受体Nur77是一种脂毒性传感器,可调节胰腺β细胞中葡萄糖诱导的胰岛素分泌。
Mol Endocrinol. 2012 Mar;26(3):399-413. doi: 10.1210/me.2011-1317. Epub 2012 Feb 2.
8
Quantitative Phosphoproteomic Analysis Reveals the Regulatory Networks of on Lipid and Glucose Metabolism in Zebrafish.定量磷酸化蛋白质组学分析揭示了在斑马鱼脂质和糖代谢中的调控网络。
Int J Mol Sci. 2020 Apr 19;21(8):2860. doi: 10.3390/ijms21082860.
9
Integrated Metabolomics and Lipidomics Analysis Reveal Remodeling of Lipid Metabolism and Amino Acid Metabolism in Glucagon Receptor-Deficient Zebrafish.整合代谢组学和脂质组学分析揭示胰高血糖素受体缺陷型斑马鱼脂质代谢和氨基酸代谢的重塑
Front Cell Dev Biol. 2021 Jan 14;8:605979. doi: 10.3389/fcell.2020.605979. eCollection 2020.
10
Nur77 suppresses hepatocellular carcinoma via switching glucose metabolism toward gluconeogenesis through attenuating phosphoenolpyruvate carboxykinase sumoylation.Nur77 通过抑制磷酸烯醇式丙酮酸羧激酶的 sumoylation 来将葡萄糖代谢转向糖异生,从而抑制肝癌。
Nat Commun. 2017 Feb 27;8:14420. doi: 10.1038/ncomms14420.

引用本文的文献

1
From Nuclear Receptor Regulation to Spleen Activating and Accumulation Resolving Therapy: A Review of Traditional Chinese Medicine Against Diabetes and Inflammation.从核受体调节到健脾消积疗法:中医药治疗糖尿病与炎症的综述
Int J Mol Sci. 2025 Jun 30;26(13):6345. doi: 10.3390/ijms26136345.
2
High glucose levels promote glycolysis and cholesterol synthesis via ERRα and suppress the autophagy-lysosomal pathway in endometrial cancer.高血糖水平通过雌激素相关受体α促进子宫内膜癌中的糖酵解和胆固醇合成,并抑制自噬-溶酶体途径。
Cell Death Dis. 2025 Mar 17;16(1):182. doi: 10.1038/s41419-025-07499-y.
3
Potential Role of NUR77 in the Aging Retinal Pigment Epithelium and Age-Related Macular Degeneration.

本文引用的文献

1
Homeostatic Regulation of Glucose Metabolism by the Central Nervous System.中枢神经系统对葡萄糖代谢的稳态调节。
Endocrinol Metab (Seoul). 2022 Feb;37(1):9-25. doi: 10.3803/EnM.2021.1364. Epub 2022 Feb 28.
2
SIRT1 selectively exerts the metabolic protective effects of hepatocyte nicotinamide phosphoribosyltransferase.SIRT1 选择性地发挥肝细胞烟酰胺磷酸核糖基转移酶的代谢保护作用。
Nat Commun. 2022 Feb 28;13(1):1074. doi: 10.1038/s41467-022-28717-7.
3
Pan-cancer analysis reveals the oncogenic role of 3-hydroxy-3-methylglutaryl-CoA synthase 1.
NUR77在衰老视网膜色素上皮及年龄相关性黄斑变性中的潜在作用
Adv Exp Med Biol. 2025;1468:165-169. doi: 10.1007/978-3-031-76550-6_27.
4
In Search of a Target Gene for a Desirable Phenotype in Aquaculture: Genome Editing of Cyprinidae and Salmonidae Species.在水产养殖中寻找理想表型的目标基因:鲤鱼科和鲑科鱼类的基因组编辑。
Genes (Basel). 2024 Jun 1;15(6):726. doi: 10.3390/genes15060726.
5
Regulation of the Nur77-P2X7r Signaling Pathway by Nodakenin: A Potential Protective Function against Alcoholic Liver Disease.Nodakenin 通过调控 Nur77-P2X7r 信号通路对酒精性肝病发挥潜在的保护作用。
Molecules. 2024 Feb 29;29(5):1078. doi: 10.3390/molecules29051078.
6
Neutrophils facilitate the epicardial regenerative response after zebrafish heart injury.中性粒细胞促进斑马鱼心脏损伤后的心外膜再生反应。
Dev Biol. 2024 Apr;508:93-106. doi: 10.1016/j.ydbio.2024.01.011. Epub 2024 Jan 28.
7
Novel Loss-of-Function Variant in HNF1a Induces β-Cell Dysfunction through Endoplasmic Reticulum Stress.新型 HNF1a 功能丧失性变异通过内质网应激诱导β细胞功能障碍。
Int J Mol Sci. 2022 Oct 27;23(21):13022. doi: 10.3390/ijms232113022.
8
Therapeutic potential of NR4A1 in cancer: Focus on metabolism.NR4A1在癌症治疗中的潜力:聚焦于代谢。
Front Oncol. 2022 Aug 16;12:972984. doi: 10.3389/fonc.2022.972984. eCollection 2022.
泛癌症分析揭示 3-羟基-3-甲基戊二酰辅酶 A 合酶 1 的致癌作用。
Cancer Rep (Hoboken). 2022 Sep;5(9):e1562. doi: 10.1002/cnr2.1562. Epub 2021 Sep 22.
4
MEF2D-NR4A1-FAM134B2-mediated reticulophagy contributes to amino acid homeostasis.MEF2D-NR4A1-FAM134B2介导的网织红细胞自噬有助于氨基酸稳态。
Autophagy. 2022 May;18(5):1049-1061. doi: 10.1080/15548627.2021.1968228. Epub 2021 Sep 14.
5
Synthesis and discovery of ω-3 polyunsaturated fatty acid- alkanolamine (PUFA-AA) derivatives as anti-inflammatory agents targeting Nur77.ω-3 多不饱和脂肪酸-烷醇胺(PUFA-AA)衍生物的合成与发现作为靶向 Nur77 的抗炎剂。
Bioorg Chem. 2020 Dec;105:104456. doi: 10.1016/j.bioorg.2020.104456. Epub 2020 Nov 8.
6
The Paradoxical Roles of Orphan Nuclear Receptor 4A (NR4A) in Cancer.孤儿核受体 4A(NR4A)在癌症中的矛盾作用。
Mol Cancer Res. 2021 Feb;19(2):180-191. doi: 10.1158/1541-7786.MCR-20-0707. Epub 2020 Oct 26.
7
Reducing Glucokinase Activity to Enhance Insulin Secretion: A Counterintuitive Theory to Preserve Cellular Function and Glucose Homeostasis.降低葡萄糖激酶活性以增强胰岛素分泌:一种维持细胞功能和葡萄糖内稳态的反直觉理论。
Front Endocrinol (Lausanne). 2020 Jun 9;11:378. doi: 10.3389/fendo.2020.00378. eCollection 2020.
8
Zebrafish models of skeletal dysplasia induced by cholesterol biosynthesis deficiency.由胆固醇生物合成缺陷引起的骨骼发育不良的斑马鱼模型。
Dis Model Mech. 2020 Jun 24;13(6):dmm042549. doi: 10.1242/dmm.042549.
9
Interaction of Nuclear Receptor Subfamily 4 Group A Member 1 (Nr4a1) and Liver Linase B1 (LKB1) Mitigates Type 2 Diabetes Mellitus by Activating Monophosphate-Activated Protein Kinase (AMPK)/Sirtuin 1 (SIRT1) Axis and Inhibiting Nuclear Factor-kappa B (NF-κB) Activation.核受体亚家族 4 组 A 成员 1(Nr4a1)与肝脂肪酶 B1(LKB1)相互作用通过激活单磷酸激活蛋白激酶(AMPK)/沉默调节蛋白 1(SIRT1)轴和抑制核因子-κB(NF-κB)激活来减轻 2 型糖尿病。
Med Sci Monit. 2020 Jan 15;26:e920278. doi: 10.12659/MSM.920278.
10
Validation of Human Sterol 14α-Demethylase (CYP51) Druggability: Structure-Guided Design, Synthesis, and Evaluation of Stoichiometric, Functionally Irreversible Inhibitors.验证人固醇 14α-脱甲基酶(CYP51)的成药性:基于结构的设计、合成及化学计量比、功能不可逆抑制剂的评价。
J Med Chem. 2019 Nov 27;62(22):10391-10401. doi: 10.1021/acs.jmedchem.9b01485. Epub 2019 Nov 11.