[1]王佳蓓 陈风 刘莹 王涤非.Nur77与物质能量代谢的关系[J].国际内分泌代谢杂志,2019,39(01):49-52.[doi:10.3760/cma.j.issn.1673-4157.2019.01.012]
 Wang Jiabei,Chen Feng,Liu Ying,et al.Relationship between Nur77 and meterial, energy metabolism[J].International Journal of Endocrinology and Metabolism,2019,39(01):49-52.[doi:10.3760/cma.j.issn.1673-4157.2019.01.012]
点击复制

Nur77与物质能量代谢的关系()
分享到:

《国际内分泌代谢杂志》[ISSN:1673-4157/CN:12-1383/R]

卷:
39
期数:
2019年01期
页码:
49-52
栏目:
综述
出版日期:
2019-01-20

文章信息/Info

Title:
Relationship between Nur77 and meterial, energy metabolism
作者:
王佳蓓1 陈风1 刘莹2 王涤非1
1中国医科大学附属第一医院老年医学内分泌科,沈阳 110001; 2中国医科大学,沈阳 110013
Author(s):
Wang Jiabei1 Chen Feng1 Liu Ying2 Wang Difei1
1Department of Geriatrics, The First Hospital of Shenyang, Shengyang 110001, China; 2China Medical University, Shenyang 110013, China
关键词:
Nur77 葡萄糖代谢 脂代谢 能量代谢 代谢性疾病
Keywords:
Nur77 Glucose metabolism Lipid metabolism Energy metabolism Metabolic diseases
DOI:
10.3760/cma.j.issn.1673-4157.2019.01.012
摘要:
Nur77是孤儿核受体,也是由配体激活的转录因子,其表达可激活或者抑制下游基因转录。Nur77能够调控糖原合成,是激素调控下游代谢基因途径中不可或缺的中间环节; 也可能与脂肪细胞分化中一些相关基因存在交叉反应,从而在脂肪细胞分化中产生重要作用; 还是机体维持能量平衡的重要调控因子。Nur77可调节糖代谢、脂代谢、能量代谢甚至与代谢性疾病密切相关。因此,许多可激动Nur77的合成或天然化学物质可能是未来治疗代谢性疾病的潜在药物。
Abstract:
Nur77 is an orphan nuclear receptor and a ligand-activated transcription factor whose expression activates or inhibits downstream gene transcription. Nur77, which can regulate glycogen synthesis, is an indispensable intermediate link in hormone regulation of downstream metabolic gene pathway. There may also be cross-reactions with some genes related to adipocyte differentiation, which may play important roles in adipocyte differentiation, and are also important regulatory factors for maintaining energy balance in the body. Nur77 regulates glucose metabolism,lipid metabolism, energy metabolism and even metabolic diseases. Therefore, many exciting synthetic or natural chemicals of Nur77 may be potential drugs for the treatment of metabolic diseases in the future.

参考文献/References:

[1] Li XX,Wang ZJ,Zheng Y,et al.Nuclear receptor Nur77 facilitates melanoma cell survival under metabolic stress by protecting fatty acid oxidation[J].Mol Cell,2018,69(3):480-492.e7.DOI:10.1016/j.molcel.2018.01.001.
[2] Liu J,Wang GH,Duan YH,et al.Modulation of the Nur77-Bcl-2 apoptotic pathway by p38α MAPK[J].Oncotarget,2017,8(41):69731-69745.DOI:10.18632/oncotarget.19227.
[3] Bian XL,Chen HZ,Yang PB,et al. Nur77 suppresses hepatocellular carcinoma via switching glucose metabolism toward gluconeogenesis through attenuating phosphoenolpyruvate carboxykinase sumoylation[J].Nat Commun,2017,8:14420.DOI:10.1038/ncomms14420.
[4] Cortez-Toledo O,Schnair C,Sangngern P,et al.Nur77 deletion impairs muscle growth during developmental myogenesis and muscleregeneration in mice[J].PLoS One,2017,12(2):e0171268.DOI:10.1371/journal.pone.0171268.
[5] Tontonoz P,Cortez-Toledo O,Wroblewski K,et al.The orphan nuclear receptor Nur77 is a determinant of myofiber size and muscle mass in mice[J].Mol Cell Biol,2015,35(7):1125-1138.DOI:10.1128/MCB.00715-14.
[6] Constantinescu S,Turcotte LP.Amelioration of palmitate-induced metabolic dysfunction in L6 muscle cells expressing low levels of receptor-interacting protein 140[J].Can J Physiol Pharmacol,2015,93(11):913-922.DOI:10.1139/cjpp-2015-0020.
[7] Yarimizu D,Doi M,Ota T,et al.Stimulus-selective induction of the orphan nuclear receptor NGFIB underlies different influences of angiotensin Ⅱ and potassium on the human adrenal gland zona glomerulosa-specific 3β-HSD isoform gene expression in adrenocortical H295R cells[J].Endocr J,2015,62(9):765-776.DOI:10.1507/endocrj.EJ15-0211.
[8] Lee BH,Indran IR,Tan HM,et al.A dietary medium-chain fatty acid, decanoic acid, inhibits recruitment of Nur77 to the HSD3B2 promoter in vitro and reverses endocrine and metabolic abnormalities in a rat model of polycystic ovary syndrome[J].Endocrinology,2016,157(1):382-394.DOI:10.1210/en.2015-1733.
[9] Yu C,Cui S,Zong C,et al.The orphan nuclear receptor NR4A1 protects pancreatic β-cells from Endoplasmic Reticulum(ER)stress-mediated apoptosis[J].J Biol Chem,2015,290(34):20687-20699.DOI:10.1074/jbc.M115.654863.
[10] Reynolds MS,Hancock CR,Ray JD,et al.β-Cell deletion of Nr4a1 and Nr4a3 nuclear receptors impedes mitochondrial respiration and insulin secretion[J].Am J Physiol Endocrinol Metab,2016,311(1):E186-E201.DOI:10.1152/ajpendo.00022.2016.
[11] Ray JD,Kener KB,Bitner BF,et al.Nkx6.1-mediated insulin secretion and β-cell proliferation is dependent on upregulation of c-Fos[J].FEBS Lett,2016,590(12):1791-1803.DOI:10.1002/1873-3468.12208.
[12] Hu Y,Zhan Q,Liu HX,et al.Accelerated partial hepatectomy-induced liver cell proliferation is associated with liver injury in Nur77 knockout mice[J].Am J Pathol,2014,184(12):3272-3283.DOI:10.1016/j.ajpath.2014.08.002.
[13] Fleuren WW,Linssen MM,Toonen EJ,et al.Prednisolone induces the Wnt signalling pathway in 3T3-L1 adipocytes[J].Arch Physiol Biochem,2013,119(2):52-64.DOI:10.3109/13813455.2013.774022.
[14] Tsai YC,Yang BC,Peng WH,et al.Heme oxygenase-1 mediates anti-adipogenesis effect of raspberry ketone in 3T3-L1 cells[J].Phytomedicine,2017,31:11-17.DOI:10.1016/j.phymed.2017.05.005.
[15] Perez-Sieira S,Martinez G,Porteiro B,et al.Female Nur77-deficient mice show increased susceptibility to diet-induced obesity[J].PLoS One,2013,8(1):e53836.DOI:10.1371/journal.pone.0053836.
[16] Lee BH,Indran IR,Tan HM,et al.A dietary medium-chain fatty acid, decanoic acid, inhibits recruitment of Nur77 to the HSD3B2 promoter in vitro and reverses endocrine and metabolic abnormalities in a rat model of polycystic ovary syndrome[J].Endocrinology,2016,157(1):382-394.DOI:10.1210/en.2015-1733.
[17] Zhou F,Bai M,Zhang Y,et al.Berberine-induced activation of AMPK increases hepatic FGF21 expression via NUR77[J].Biochem Biophys Res Commun,2018,495(2):1936-1941.DOI:10.1016/j.bbrc.2017.12.070.
[18] Chen Y,Wu R,Chen HZ,et al.Enhancement of hypothalamic STAT3 acetylation by nuclear receptor Nur77 dictates leptin sensitivity[J].Diabetes,2015,64(6):2069-2081.DOI:10.2337/db14-1206.
[19] Rodríguez-Calvo R,Tajes M,Vázquez-Carrera M.The NR4A subfamily of nuclear receptors: potential new therapeutic targets for the treatment of inflammatory diseases[J].Expert Opin Ther Targets,2017,21(3):291-304.DOI:10.1080/14728222.2017.1279146.
[20] Chen YT,Liao JW,Tsai YC,et al.Inhibition of DNA methyltransferase 1 increases nuclear receptor subfamily 4 group A member 1 expression and decreases blood glucose in type 2 diabetes[J].Oncotarget,2016,7(26):39162-39170.DOI:10.18632/oncotarget.10043.
[21] Zhao N,Li X,Feng Y,et al.The nuclear orphan receptor Nur77 alleviates palmitate-induced fat accumulation by down-regulating G0S2 in HepG2 cells[J].Sci Rep,2018,8(1):4809.DOI:10.1038/s41598-018-23141-8.
[22] Chen Y,Wu R,Chen HZ,et al.Enhancement of hypothalamic STAT3 acetylation by nuclear receptor Nur77 dictates leptin sensitivity[J].Diabetes,2015,64(6):2069-2081.DOI:10.2337/db14-1206.
[23] Shao Q,Han F,Peng S,et al.Nur77 inhibits oxLDL induced apoptosis of macrophages via the p38 MAPK signaling pathway[J].Biochem Biophys Res Commun,2016,471(4):633-638.DOI:10.1016/j.bbrc.2016.01.004.
[24] Hamers AA,Argmann C,Moerland PD,et al.Nur77-deficiency in bone marrow-derived macrophages modulates inflammatory responses, extracellular matrix homeostasis, phagocytosis and tolerance[J].BMC Genomics,2016,17:162.DOI:10.1186/s12864-016-2469-9.

相似文献/References:

[1]项芬芬,张学梅,高英慧,等.p53与物质能量代谢的关系[J].国际内分泌代谢杂志,2017,37(04):262.
 Xiang Fenfen*,Zhang Xuemei,Gao Yinghui,et al.Relationship between p53 and material, energy metabolism[J].International Journal of Endocrinology and Metabolism,2017,37(01):262.

备注/Memo

备注/Memo:
通信作者:王涤非,Email:wdf8lm@qq.com
基金项目:国家自然科学基金(31570819); 辽宁省科技计划项目(2015225024); 中央支持地方科技引导项目(2016007024)
Corresponding author: Wang Difei, Email:wdf8lm@qq.com
Fund program:National Natural Science Foundation of China(31570819); Liaoning Science and Technology Plan Project(2015225024); The Central Government Supports Local Science and Technology Guidance Projects(2016007024)
更新日期/Last Update: 2019-01-20