• 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

mTOR 信号通路与各种疾病中的肠道微生物群:药物治疗中的机制和潜在药物。

mTOR Signaling Pathway and Gut Microbiota in Various Disorders: Mechanisms and Potential Drugs in Pharmacotherapy.

机构信息

College of Life Science and Bioengineering, Beijing Jiaotong University, Beijing 100044, China.

出版信息

Int J Mol Sci. 2023 Jul 22;24(14):11811. doi: 10.3390/ijms241411811.

DOI:10.3390/ijms241411811
PMID:37511569
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10380532/
Abstract

The mammalian or mechanistic target of rapamycin (mTOR) integrates multiple intracellular and extracellular upstream signals involved in the regulation of anabolic and catabolic processes in cells and plays a key regulatory role in cell growth and metabolism. The activation of the mTOR signaling pathway has been reported to be associated with a wide range of human diseases. A growing number of in vivo and in vitro studies have demonstrated that gut microbes and their complex metabolites can regulate host metabolic and immune responses through the mTOR pathway and result in disorders of host physiological functions. In this review, we summarize the regulatory mechanisms of gut microbes and mTOR in different diseases and discuss the crosstalk between gut microbes and their metabolites and mTOR in disorders in the gastrointestinal tract, liver, heart, and other organs. We also discuss the promising application of multiple potential drugs that can adjust the gut microbiota and mTOR signaling pathways. Despite the limited findings between gut microbes and mTOR, elucidating their relationship may provide new clues for the prevention and treatment of various diseases.

摘要

哺乳动物雷帕霉素靶蛋白(mTOR)整合了参与细胞中合成代谢和分解代谢过程调节的多种细胞内和细胞外上游信号,并在细胞生长和代谢中发挥关键调节作用。据报道,mTOR 信号通路的激活与广泛的人类疾病有关。越来越多的体内和体外研究表明,肠道微生物及其复杂代谢产物可以通过 mTOR 途径调节宿主代谢和免疫反应,并导致宿主生理功能障碍。在这篇综述中,我们总结了肠道微生物和 mTOR 在不同疾病中的调节机制,并讨论了肠道微生物及其代谢物与 mTOR 之间在胃肠道、肝脏、心脏和其他器官紊乱中的相互作用。我们还讨论了多种可能的药物的有前途的应用,这些药物可以调节肠道微生物群和 mTOR 信号通路。尽管肠道微生物和 mTOR 之间的发现有限,但阐明它们之间的关系可能为预防和治疗各种疾病提供新的线索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b409/10380532/62d8657d4463/ijms-24-11811-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b409/10380532/dcfeee932562/ijms-24-11811-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b409/10380532/dadc88ce2a17/ijms-24-11811-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b409/10380532/62d8657d4463/ijms-24-11811-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b409/10380532/dcfeee932562/ijms-24-11811-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b409/10380532/dadc88ce2a17/ijms-24-11811-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b409/10380532/62d8657d4463/ijms-24-11811-g003.jpg

相似文献

1
mTOR Signaling Pathway and Gut Microbiota in Various Disorders: Mechanisms and Potential Drugs in Pharmacotherapy.mTOR 信号通路与各种疾病中的肠道微生物群:药物治疗中的机制和潜在药物。
Int J Mol Sci. 2023 Jul 22;24(14):11811. doi: 10.3390/ijms241411811.
2
Gut microbiota and mTOR signaling: Insight on a new pathophysiological interaction.肠道微生物群和 mTOR 信号:对新的病理生理相互作用的洞察。
Microb Pathog. 2018 May;118:98-104. doi: 10.1016/j.micpath.2018.03.021. Epub 2018 Mar 13.
3
Mammalian target of rapamycin: a central node of complex signaling cascades.雷帕霉素的哺乳动物靶点:复杂信号级联反应的核心节点。
Int J Clin Exp Pathol. 2011 Jun 20;4(5):476-95. Epub 2011 Jun 14.
4
Nutrient regulation of mTORC1 at a glance.mTORC1 的营养素调控一览
J Cell Sci. 2019 Nov 13;132(21):jcs222570. doi: 10.1242/jcs.222570.
5
Sensing of nutrients and microbes in the gut.肠道对营养物质和微生物的感知。
Curr Opin Gastroenterol. 2016 Mar;32(2):86-95. doi: 10.1097/MOG.0000000000000246.
6
mTOR Pathway is Involved in Energy Homeostasis Regulation as a Part of the Gut-Brain Axis.mTOR 通路作为肠脑轴的一部分参与能量稳态调节。
Int J Mol Sci. 2020 Aug 10;21(16):5715. doi: 10.3390/ijms21165715.
7
Regulatory effect of orexin system on various diseases through mTOR signaling pathway.食欲素系统通过mTOR信号通路对多种疾病的调节作用。
Trends Endocrinol Metab. 2023 May;34(5):292-302. doi: 10.1016/j.tem.2023.02.008. Epub 2023 Mar 16.
8
mTOR signaling for biological control and cancer.mTOR 信号通路在生物调控和癌症中的作用
J Cell Physiol. 2013 Aug;228(8):1658-64. doi: 10.1002/jcp.24351.
9
Mammalian target of rapamycin (mTOR) pathways in neurological diseases.哺乳动物雷帕霉素靶蛋白(mTOR)通路与神经退行性疾病。
Biomed J. 2013 Mar-Apr;36(2):40-50. doi: 10.4103/2319-4170.110365.
10
Mechanistic target of rapamycin (mTOR): a potential new therapeutic target for rheumatoid arthritis.雷帕霉素靶蛋白(mTOR):类风湿关节炎潜在的新治疗靶点。
Arthritis Res Ther. 2023 Oct 2;25(1):187. doi: 10.1186/s13075-023-03181-w.

引用本文的文献

1
Eukaryotic initiation factors: central factor associating mRNA translational plasticity during neuropathic pain progression.真核生物起始因子:在神经性疼痛进展过程中与mRNA翻译可塑性相关的核心因子。
Front Neurol. 2025 Jul 30;16:1566205. doi: 10.3389/fneur.2025.1566205. eCollection 2025.
2
Immunosuppressants Rewire the Gut Microbiome-Alloimmune Axis Through Time-Dependent and Tissue-Specific Mechanisms.免疫抑制剂通过时间依赖性和组织特异性机制重塑肠道微生物群-同种免疫轴。
bioRxiv. 2025 Jul 11:2025.01.02.631100. doi: 10.1101/2025.01.02.631100.
3
Multi-omics profile of exceptional long-term survivors of AJCC stage III triple-negative breast cancer.

本文引用的文献

1
Maltol attenuates polystyrene nanoplastic-induced enterotoxicity by promoting AMPK/mTOR/TFEB-mediated autophagy and modulating gut microbiota.麦芽酚通过促进AMPK/mTOR/TFEB介导的自噬和调节肠道微生物群来减轻聚苯乙烯纳米塑料诱导的肠毒性。
Environ Pollut. 2023 Apr 1;322:121202. doi: 10.1016/j.envpol.2023.121202. Epub 2023 Feb 7.
2
Integrated analysis of the gut microbiome and metabolome in a mouse model of inflammation-induced colorectal tumors.炎症诱导的结直肠癌小鼠模型中肠道微生物组和代谢组的综合分析
Front Microbiol. 2023 Jan 13;13:1082835. doi: 10.3389/fmicb.2022.1082835. eCollection 2022.
3
Structure of the lysosomal mTORC1-TFEB-Rag-Ragulator megacomplex.
美国癌症联合委员会(AJCC)III期三阴性乳腺癌长期生存者的多组学特征
Chin J Cancer Res. 2025 Jun 30;37(3):316-336. doi: 10.21147/j.issn.1000-9604.2025.03.03.
4
Gut microbiome and host TOR pathway interact to regulate predator-induced aversive memory in .肠道微生物群与宿主的TOR通路相互作用,以调节(某种生物中)捕食者诱导的厌恶记忆。
Proc Natl Acad Sci U S A. 2025 Jun 24;122(25):e2422928122. doi: 10.1073/pnas.2422928122. Epub 2025 Jun 20.
5
Targeting the programmed cell death signaling mechanism with natural products for the treatment of acute pancreatitis: a review.以天然产物靶向程序性细胞死亡信号机制治疗急性胰腺炎:综述
Front Pharmacol. 2025 May 30;16:1567552. doi: 10.3389/fphar.2025.1567552. eCollection 2025.
6
Structure-Based Modeling of the Gut Bacteria-Host Interactome Through Statistical Analysis of Domain-Domain Associations Using Machine Learning.通过机器学习对结构域-结构域关联进行统计分析,基于结构的肠道细菌-宿主相互作用组建模。
BioTech (Basel). 2025 Feb 25;14(1):13. doi: 10.3390/biotech14010013.
7
Exploring Protein Functions of Gut Bacteriome and Mycobiome in Thai Infants Associated with Atopic Dermatitis Through Metaproteomic and Host Interaction Analysis.通过元蛋白质组学和宿主相互作用分析探索泰国特应性皮炎婴儿肠道细菌群落和真菌群落的蛋白质功能
Int J Mol Sci. 2024 Dec 18;25(24):13533. doi: 10.3390/ijms252413533.
8
Significance of host antimicrobial peptides in the pathogenesis and treatment of acne vulgaris.宿主抗菌肽在寻常痤疮发病机制及治疗中的意义
Front Immunol. 2024 Dec 18;15:1502242. doi: 10.3389/fimmu.2024.1502242. eCollection 2024.
9
Gut-brain axis and brain health: modulating neuroinflammation, cognitive decline, and neurodegeneration.肠-脑轴与脑健康:调节神经炎症、认知衰退和神经退行性变。
3 Biotech. 2025 Jan;15(1):25. doi: 10.1007/s13205-024-04187-0. Epub 2024 Dec 27.
10
mTOR and SGLT-2 Inhibitors: Their Synergistic Effect on Age-Related Processes.mTOR 和 SGLT-2 抑制剂:它们在与年龄相关的过程中的协同作用。
Int J Mol Sci. 2024 Aug 8;25(16):8676. doi: 10.3390/ijms25168676.
溶酶体 mTORC1-TFEB-Rag-Ragulator 巨型复合物的结构。
Nature. 2023 Feb;614(7948):572-579. doi: 10.1038/s41586-022-05652-7. Epub 2023 Jan 25.
4
Regulation of gut microbiome by ketogenic diet in neurodegenerative diseases: A molecular crosstalk.生酮饮食对神经退行性疾病肠道微生物群的调节作用:分子间的相互作用
Front Aging Neurosci. 2022 Oct 14;14:1015837. doi: 10.3389/fnagi.2022.1015837. eCollection 2022.
5
Theabrownin Alleviates Colorectal Tumorigenesis in Murine AOM/DSS Model via PI3K/Akt/mTOR Pathway Suppression and Gut Microbiota Modulation.茶褐素通过抑制PI3K/Akt/mTOR信号通路和调节肠道微生物群减轻小鼠AOM/DSS模型中的结直肠癌发生。
Antioxidants (Basel). 2022 Aug 30;11(9):1716. doi: 10.3390/antiox11091716.
6
Low-dose radiation exaggerates HFD-induced metabolic dysfunction by gut microbiota through PA-PYCR1 axis.低剂量辐射通过 PA-PYCR1 轴通过肠道微生物群夸大 HFD 诱导的代谢功能障碍。
Commun Biol. 2022 Sep 10;5(1):945. doi: 10.1038/s42003-022-03929-1.
7
Structure of the nutrient-sensing hub GATOR2.营养感应枢纽 GATOR2 的结构。
Nature. 2022 Jul;607(7919):610-616. doi: 10.1038/s41586-022-04939-z. Epub 2022 Jul 13.
8
Interaction effect between NAFLD severity and high carbohydrate diet on gut microbiome alteration and hepatic lipogenesis.非酒精性脂肪性肝病严重程度和高碳水化合物饮食对肠道微生物组改变和肝内脂质生成的交互作用。
Gut Microbes. 2022 Jan-Dec;14(1):2078612. doi: 10.1080/19490976.2022.2078612.
9
Huangqin decoction ameliorates DSS-induced ulcerative colitis: Role of gut microbiota and amino acid metabolism, mTOR pathway and intestinal epithelial barrier.黄芩汤改善右旋糖酐硫酸酯钠诱导的溃疡性结肠炎:肠道微生物群和氨基酸代谢、mTOR 通路及肠上皮屏障的作用
Phytomedicine. 2022 Jun;100:154052. doi: 10.1016/j.phymed.2022.154052. Epub 2022 Mar 14.
10
Changes of gut microbiota in diabetic nephropathy and its effect on the progression of kidney injury.糖尿病肾病中肠道微生物群的变化及其对肾损伤进展的影响。
Endocrine. 2022 May;76(2):294-303. doi: 10.1007/s12020-022-03002-1. Epub 2022 Mar 4.