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代谢组学在胰岛营养感应机制中的应用。

Metabolomics applied to islet nutrient sensing mechanisms.

机构信息

Sarah W. Stedman Nutrition and Metabolism Center, Duke Molecular Physiology Institute, Duke University Medical Center, Durham, North Carolina.

Department of Pharmacology and Alberta Diabetes Institute, University of Alberta, Edmonton, Canada.

出版信息

Diabetes Obes Metab. 2017 Sep;19 Suppl 1(Suppl 1):90-94. doi: 10.1111/dom.13010.

DOI:10.1111/dom.13010
PMID:28880482
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5929146/
Abstract

After multiple decades of investigation, the precise mechanisms involved in fuel-stimulated insulin secretion are still being revealed. One avenue for gaining deeper knowledge is to apply emergent tools of "metabolomics," involving mass spectrometry and nuclear magnetic resonance-based profiling of islet cells in their fuel-stimulated compared with basal states. The current article summarizes recent insights gained from application of metabolomics tools to the specific process of glucose-stimulated insulin secretion, revealing 2 new mechanisms that may provide targets for improving insulin secretion in diabetes.

摘要

经过几十年的研究,燃料刺激胰岛素分泌的确切机制仍在不断揭示。深入了解这一过程的一个途径是应用新兴的“代谢组学”工具,这些工具涉及对受燃料刺激和基础状态下的胰岛细胞进行质谱和基于核磁共振的分析。本文总结了代谢组学工具在葡萄糖刺激胰岛素分泌这一特定过程中的最新应用所获得的新见解,揭示了 2 种新的机制,这些机制可能为改善糖尿病中的胰岛素分泌提供靶点。

相似文献

1
Metabolomics applied to islet nutrient sensing mechanisms.代谢组学在胰岛营养感应机制中的应用。
Diabetes Obes Metab. 2017 Sep;19 Suppl 1(Suppl 1):90-94. doi: 10.1111/dom.13010.
2
Time-resolved metabolomics analysis of β-cells implicates the pentose phosphate pathway in the control of insulin release.时间分辨代谢组学分析β细胞表明戊糖磷酸途径在胰岛素分泌控制中的作用。
Biochem J. 2013 Mar 15;450(3):595-605. doi: 10.1042/BJ20121349.
3
Metabolomics Analysis of Nutrient Metabolism in β-Cells.β 细胞中营养代谢的代谢组学分析。
J Mol Biol. 2020 Mar 6;432(5):1429-1445. doi: 10.1016/j.jmb.2019.07.020. Epub 2019 Jul 17.
4
Human islet preparations distributed for research exhibit a variety of insulin-secretory profiles.用于研究的人胰岛制剂呈现出多种胰岛素分泌模式。
Am J Physiol Endocrinol Metab. 2015 Apr 1;308(7):E592-602. doi: 10.1152/ajpendo.00437.2014. Epub 2015 Feb 3.
5
Adenylosuccinate Is an Insulin Secretagogue Derived from Glucose-Induced Purine Metabolism.腺苷酸琥珀酸是一种由葡萄糖诱导的嘌呤代谢产生的胰岛素分泌促进剂。
Cell Rep. 2015 Oct 6;13(1):157-167. doi: 10.1016/j.celrep.2015.08.072. Epub 2015 Sep 24.
6
Islet acid glucan-1,4-alpha-glucosidase: a putative key enzyme in nutrient-stimulated insulin secretion.胰岛酸性葡聚糖-1,4-α-葡萄糖苷酶:营养物质刺激胰岛素分泌中的一种假定关键酶。
Endocrinology. 1996 Apr;137(4):1219-25. doi: 10.1210/endo.137.4.8625892.
7
Defective Amplifying Pathway of β-Cell Secretory Response to Glucose in Type 2 Diabetes: Integrated Modeling of In Vitro and In Vivo Evidence.2 型糖尿病β细胞分泌反应对葡萄糖的放大途径缺陷:体外和体内证据的综合建模。
Diabetes. 2018 Mar;67(3):496-506. doi: 10.2337/db17-1039. Epub 2017 Dec 11.
8
Overexpression of mitochondrial FAD-linked glycerol-3-phosphate dehydrogenase does not correct glucose-stimulated insulin secretion from diabetic GK rat pancreatic islets.线粒体黄素腺嘌呤二核苷酸(FAD)连接的甘油-3-磷酸脱氢酶的过表达并不能纠正糖尿病GK大鼠胰岛中葡萄糖刺激的胰岛素分泌。
Diabetologia. 1998 Jun;41(6):649-53. doi: 10.1007/s001250050963.
9
Quantitative Phosphoproteomics Revealed Glucose-Stimulated Responses of Islet Associated with Insulin Secretion.定量磷酸化蛋白质组学揭示了与胰岛素分泌相关的胰岛的葡萄糖刺激反应。
J Proteome Res. 2015 Nov 6;14(11):4635-46. doi: 10.1021/acs.jproteome.5b00507. Epub 2015 Oct 15.
10
Tacrolimus impairment of insulin secretion in isolated rat islets occurs at multiple distal sites in stimulus-secretion coupling.他克莫司对分离的大鼠胰岛胰岛素分泌的损害发生在刺激-分泌偶联的多个远端位点。
Endocrinology. 2004 May;145(5):2264-72. doi: 10.1210/en.2003-1152. Epub 2004 Feb 12.

引用本文的文献

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Metabolic and Molecular Amplification of Insulin Secretion.胰岛素分泌的代谢和分子放大。
Adv Anat Embryol Cell Biol. 2024;239:117-139. doi: 10.1007/978-3-031-62232-8_5.
2
Checkpoint kinase 2 controls insulin secretion and glucose homeostasis.细胞周期检测点激酶 2 控制胰岛素分泌和葡萄糖内稳定。
Nat Chem Biol. 2024 May;20(5):566-576. doi: 10.1038/s41589-023-01466-4. Epub 2023 Nov 9.
3
Investigation of the Exometabolomic Profiles of Rat Islets of Langerhans Cultured in Microfluidic Biochip.微流控生物芯片中培养的大鼠胰岛外代谢组学特征研究。

本文引用的文献

1
SUMOylation and calcium control syntaxin-1A and secretagogin sequestration by tomosyn to regulate insulin exocytosis in human ß cells.SUMOylation 和钙控制突触融合蛋白 1A 和分泌颗粒相关蛋白通过 tomosyn 隔离来调节人β细胞胰岛素的胞吐作用。
Sci Rep. 2017 Mar 21;7(1):248. doi: 10.1038/s41598-017-00344-z.
2
Metabolomics and Metabolic Diseases: Where Do We Stand?代谢组学与代谢性疾病:我们目前的状况如何?
Cell Metab. 2017 Jan 10;25(1):43-56. doi: 10.1016/j.cmet.2016.09.018. Epub 2016 Oct 27.
3
Adenylosuccinate Is an Insulin Secretagogue Derived from Glucose-Induced Purine Metabolism.
Metabolites. 2022 Dec 15;12(12):1270. doi: 10.3390/metabo12121270.
4
The Human Islet: Mini-Organ With Mega-Impact.人类胰岛:迷你器官,巨大影响。
Endocr Rev. 2021 Sep 28;42(5):605-657. doi: 10.1210/endrev/bnab010.
5
GPCRs, G Proteins, and Their Impact on β-cell Function.G 蛋白偶联受体(GPCRs)、G 蛋白及其对β细胞功能的影响。
Compr Physiol. 2020 Mar 12;10(2):453-490. doi: 10.1002/cphy.c190028.
6
Intact pancreatic islets and dispersed beta-cells both generate intracellular calcium oscillations but differ in their responsiveness to glucose.完整胰岛和分散的β细胞都能产生细胞内钙振荡,但对葡萄糖的反应性不同。
Cell Calcium. 2019 Nov;83:102081. doi: 10.1016/j.ceca.2019.102081. Epub 2019 Sep 16.
7
Lipid-associated metabolic signalling networks in pancreatic beta cell function.脂相关代谢信号网络在胰腺β细胞功能中的作用。
Diabetologia. 2020 Jan;63(1):10-20. doi: 10.1007/s00125-019-04976-w. Epub 2019 Aug 19.
8
The Metabolomic Signatures of Weight Change.体重变化的代谢组学特征
Metabolites. 2019 Apr 4;9(4):67. doi: 10.3390/metabo9040067.
9
Glucose-dependent trans-plasma membrane electron transport and p70 phosphorylation in skeletal muscle cells.葡萄糖依赖的跨浆膜电子传递和骨骼肌细胞中的 p70 磷酸化。
Redox Biol. 2019 Oct;27:101075. doi: 10.1016/j.redox.2018.101075. Epub 2018 Dec 12.
10
Remodeling of the Acetylproteome by SIRT3 Manipulation Fails to Affect Insulin Secretion or β Cell Metabolism in the Absence of Overnutrition.SIRT3 操作引起的乙酰化蛋白质组重塑在不过度营养的情况下无法影响胰岛素分泌或β细胞代谢。
Cell Rep. 2018 Jul 3;24(1):209-223.e6. doi: 10.1016/j.celrep.2018.05.088.
腺苷酸琥珀酸是一种由葡萄糖诱导的嘌呤代谢产生的胰岛素分泌促进剂。
Cell Rep. 2015 Oct 6;13(1):157-167. doi: 10.1016/j.celrep.2015.08.072. Epub 2015 Sep 24.
4
Integrated, Step-Wise, Mass-Isotopomeric Flux Analysis of the TCA Cycle.三羧酸循环的整合、逐步、质量同位素异构体通量分析
Cell Metab. 2015 Nov 3;22(5):936-47. doi: 10.1016/j.cmet.2015.08.021. Epub 2015 Sep 24.
5
Isocitrate-to-SENP1 signaling amplifies insulin secretion and rescues dysfunctional β cells.异柠檬酸至SENP1信号传导增强胰岛素分泌并挽救功能失调的β细胞。
J Clin Invest. 2015 Oct 1;125(10):3847-60. doi: 10.1172/JCI82498. Epub 2015 Sep 21.
6
Metabolomics applied to the pancreatic islet.代谢组学在胰岛中的应用。
Arch Biochem Biophys. 2016 Jan 1;589:120-30. doi: 10.1016/j.abb.2015.06.013. Epub 2015 Jun 25.
7
Defining the metabolome: size, flux, and regulation.定义代谢组:规模、通量与调控
Mol Cell. 2015 May 21;58(4):699-706. doi: 10.1016/j.molcel.2015.04.021.
8
Generation of functional human pancreatic β cells in vitro.体外生成功能性人胰腺β细胞。
Cell. 2014 Oct 9;159(2):428-39. doi: 10.1016/j.cell.2014.09.040.
9
Reversal of diabetes with insulin-producing cells derived in vitro from human pluripotent stem cells.体外诱导人多能干细胞分化为胰岛素分泌细胞逆转糖尿病。
Nat Biotechnol. 2014 Nov;32(11):1121-33. doi: 10.1038/nbt.3033. Epub 2014 Sep 11.
10
Quantitative flux analysis reveals folate-dependent NADPH production.定量通量分析揭示了叶酸依赖性 NADPH 的产生。
Nature. 2014 Jun 12;510(7504):298-302. doi: 10.1038/nature13236. Epub 2014 May 4.