• 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

相似文献

1
Regulation of lipid stores and metabolism by lipophagy.脂噬作用对脂库和脂代谢的调控。
Cell Death Differ. 2013 Jan;20(1):3-11. doi: 10.1038/cdd.2012.63. Epub 2012 May 18.
2
Lipophagy and liver disease: New perspectives to better understanding and therapy.脂噬作用与肝脏疾病:更好理解和治疗的新视角。
Biomed Pharmacother. 2018 Jan;97:339-348. doi: 10.1016/j.biopha.2017.07.168. Epub 2017 Nov 6.
3
The regulation, function, and role of lipophagy, a form of selective autophagy, in metabolic disorders.脂噬作用(一种选择性自噬形式)在代谢紊乱中的调节、功能和作用。
Cell Death Dis. 2022 Feb 8;13(2):132. doi: 10.1038/s41419-022-04593-3.
4
Regulation and Functions of Autophagic Lipolysis.自噬性脂肪分解的调节与功能
Trends Endocrinol Metab. 2016 Oct;27(10):696-705. doi: 10.1016/j.tem.2016.06.003. Epub 2016 Jun 27.
5
Lipophagy-derived fatty acids undergo extracellular efflux via lysosomal exocytosis.自噬衍生的脂肪酸通过溶酶体胞吐作用进行细胞外流出。
Autophagy. 2021 Mar;17(3):690-705. doi: 10.1080/15548627.2020.1728097. Epub 2020 Feb 19.
6
Autophagy and Lipid Metabolism.自噬与脂代谢。
Adv Exp Med Biol. 2019;1206:359-374. doi: 10.1007/978-981-15-0602-4_17.
7
Autophagy and Lipid Droplets in the Liver.肝脏中的自噬与脂滴
Annu Rev Nutr. 2015;35:215-37. doi: 10.1146/annurev-nutr-071813-105336. Epub 2015 May 6.
8
Telemetric control of peripheral lipophagy by hypothalamic autophagy.下丘脑自噬对外周脂肪吞噬的遥测控制
Autophagy. 2016 Aug 2;12(8):1404-5. doi: 10.1080/15548627.2016.1185578. Epub 2016 Jun 24.
9
SB2301-mediated perturbation of membrane composition in lipid droplets induces lipophagy and lipid droplets ubiquitination.SB2301 介导的脂滴膜成分扰动诱导脂噬和脂滴泛素化。
Commun Biol. 2023 Mar 21;6(1):300. doi: 10.1038/s42003-023-04682-9.
10
Hypothalamic lipophagy and energetic balance.下丘脑脂质自噬与能量平衡。
Aging (Albany NY). 2011 Oct;3(10):934-42. doi: 10.18632/aging.100393.

引用本文的文献

1
Targeting Lipophagy in Liver Diseases: Impact on Oxidative Stress and Steatohepatitis.靶向肝脏疾病中的脂质自噬:对氧化应激和脂肪性肝炎的影响
Antioxidants (Basel). 2025 Jul 24;14(8):908. doi: 10.3390/antiox14080908.
2
Metabolic regulation of key developmental events during mammalian embryogenesis.哺乳动物胚胎发生过程中关键发育事件的代谢调控。
Nat Cell Biol. 2025 Jul 22. doi: 10.1038/s41556-025-01720-y.
3
Loss of hepatic autophagy induces α-cell proliferation through impaired glutamine-dependent gluconeogenesis.肝脏自噬的丧失通过受损的谷氨酰胺依赖性糖异生诱导α细胞增殖。
Physiol Rep. 2025 May;13(10):e70381. doi: 10.14814/phy2.70381.
4
LARS1 Promotes Tubular Epithelial Cells Epithelial Mesenchymal Transition in Chronic Kidney Disease by Inhibiting Lipophagy.LARS1通过抑制脂质自噬促进慢性肾脏病中肾小管上皮细胞的上皮-间质转化
Inflammation. 2025 May 21. doi: 10.1007/s10753-025-02313-5.
5
Crosstalk Between Autophagy and Oxidative Stress in Hematological Malignancies: Mechanisms, Implications, and Therapeutic Potential.血液系统恶性肿瘤中自噬与氧化应激的相互作用:机制、影响及治疗潜力
Antioxidants (Basel). 2025 Feb 25;14(3):264. doi: 10.3390/antiox14030264.
6
Recombinant high-density lipoprotein targeted delivery of celastrol to promote foam cells lipophagy against early atherosclerosis.重组高密度脂蛋白靶向递送雷公藤红素以促进泡沫细胞自噬对抗早期动脉粥样硬化。
J Nanobiotechnology. 2025 Mar 22;23(1):237. doi: 10.1186/s12951-025-03327-9.
7
Wash-free fluorescent tools based on organic molecules: Design principles and biomedical applications.基于有机分子的免洗荧光工具:设计原理与生物医学应用
Exploration (Beijing). 2024 Jun 28;5(1):20230094. doi: 10.1002/EXP.20230094. eCollection 2025 Feb.
8
Deciphering the anti-obesity mechanisms of pharmabiotic probiotics through advanced multiomics analysis.通过先进的多组学分析解析药物益生菌的抗肥胖机制。
iScience. 2025 Jan 25;28(2):111890. doi: 10.1016/j.isci.2025.111890. eCollection 2025 Feb 21.
9
Melanocortin 3 receptor regulates hepatic autophagy and systemic adiposity.黑皮质素3受体调节肝脏自噬和全身肥胖。
Nat Commun. 2025 Feb 16;16(1):1690. doi: 10.1038/s41467-025-56936-1.
10
Reducing microglial lipid load enhances β amyloid phagocytosis in an Alzheimer's disease mouse model.在阿尔茨海默病小鼠模型中,降低小胶质细胞脂质负荷可增强β淀粉样蛋白的吞噬作用。
Sci Adv. 2025 Feb 7;11(6):eadq6038. doi: 10.1126/sciadv.adq6038. Epub 2025 Feb 5.

本文引用的文献

1
Autophagy releases lipid that promotes fibrogenesis by activated hepatic stellate cells in mice and in human tissues.自噬释放的脂质通过激活小鼠和人组织中的肝星状细胞促进纤维化发生。
Gastroenterology. 2012 Apr;142(4):938-46. doi: 10.1053/j.gastro.2011.12.044. Epub 2012 Jan 10.
2
Obesity is associated with hypothalamic injury in rodents and humans.肥胖与啮齿动物和人类的下丘脑损伤有关。
J Clin Invest. 2012 Jan;122(1):153-62. doi: 10.1172/JCI59660. Epub 2011 Dec 27.
3
Remodeling of the arcuate nucleus energy-balance circuit is inhibited in obese mice.肥胖小鼠弓状核能量平衡回路的重塑受到抑制。
J Clin Invest. 2012 Jan;122(1):142-52. doi: 10.1172/JCI43134. Epub 2011 Dec 27.
4
Autophagy in atherosclerosis: a potential drug target for plaque stabilization.自噬在动脉粥样硬化中的作用:斑块稳定的潜在药物靶点。
Arterioscler Thromb Vasc Biol. 2011 Dec;31(12):2787-91. doi: 10.1161/ATVBAHA.111.224899.
5
Atherosclerosis: current pathogenesis and therapeutic options.动脉粥样硬化:当前的发病机制和治疗选择。
Nat Med. 2011 Nov 7;17(11):1410-22. doi: 10.1038/nm.2538.
6
GLP-1 analogs reduce hepatocyte steatosis and improve survival by enhancing the unfolded protein response and promoting macroautophagy.GLP-1 类似物通过增强未折叠蛋白反应和促进巨自噬来减少肝细胞脂肪变性并提高存活率。
PLoS One. 2011;6(9):e25269. doi: 10.1371/journal.pone.0025269. Epub 2011 Sep 21.
7
Forming functional fat: a growing understanding of adipocyte differentiation.形成功能性脂肪:对脂肪细胞分化的日益深入了解。
Nat Rev Mol Cell Biol. 2011 Sep 28;12(11):722-34. doi: 10.1038/nrm3198.
8
Peroxisome proliferation-associated control of reactive oxygen species sets melanocortin tone and feeding in diet-induced obesity.过氧化物酶体增殖物激活受体相关的活性氧控制黑素皮质素的音调并影响饮食诱导肥胖的摄食。
Nat Med. 2011 Aug 28;17(9):1121-7. doi: 10.1038/nm.2421.
9
Fatty acids suppress autophagic turnover in β-cells.脂肪酸抑制β细胞中的自噬作用。
J Biol Chem. 2011 Dec 9;286(49):42534-42544. doi: 10.1074/jbc.M111.242412. Epub 2011 Aug 21.
10
Differential roles of unsaturated and saturated fatty acids on autophagy and apoptosis in hepatocytes.不饱和脂肪酸和饱和脂肪酸对肝细胞自噬和凋亡的差异作用。
J Pharmacol Exp Ther. 2011 Nov;339(2):487-98. doi: 10.1124/jpet.111.184341. Epub 2011 Aug 19.

脂噬作用对脂库和脂代谢的调控。

Regulation of lipid stores and metabolism by lipophagy.

机构信息

Department of Medicine, Marion Bessin Liver Research Center and Diabetes Research and Training Center, Albert Einstein College of Medicine, Bronx, NY 10461, USA.

出版信息

Cell Death Differ. 2013 Jan;20(1):3-11. doi: 10.1038/cdd.2012.63. Epub 2012 May 18.

DOI:10.1038/cdd.2012.63
PMID:22595754
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3524634/
Abstract

Intracellular lipids are stored in lipid droplets (LDs) and metabolized by cytoplasmic neutral hydrolases to supply lipids for cell use. Recently, an alternative pathway of lipid metabolism through the lysosomal degradative pathway of autophagy has been described and termed lipophagy. In this form of lipid metabolism, LD triglycerides (TGs) and cholesterol are taken up by autophagosomes and delivered to lysosomes for degradation by acidic hydrolases. Free fatty acids generated by lipophagy from the breakdown of TGs fuel cellular rates of mitochondrial β-oxidation. Lipophagy therefore functions to regulate intracellular lipid stores, cellular levels of free lipids such as fatty acids and energy homeostasis. The amount of lipid metabolized by lipophagy varies in response to the extracellular supply of nutrients. The ability of the cell to alter the amount of lipid targeted for autophagic degradation depending on nutritional status demonstrates that this process is selective. Intracellular lipids themselves regulate levels of autophagy by unclear mechanisms. Impaired lipophagy can lead to excessive tissue lipid accumulation such as hepatic steatosis, alter hypothalamic neuropeptide release to affect body mass, block cellular transdifferentiation and sensitize cells to death stimuli. Future studies will likely identify additional mechanisms by which lipophagy regulates cellular physiology, making this pathway a potential therapeutic target in a variety of diseases.

摘要

细胞内脂质储存在脂滴 (LDs) 中,并通过细胞质中性水解酶代谢,为细胞利用提供脂质。最近,已经描述了一种通过自噬溶酶体降解途径的替代脂质代谢途径,并将其命名为脂噬作用。在这种脂质代谢形式中,LD 甘油三酯 (TGs) 和胆固醇被自噬体摄取,并被运送到溶酶体中,被酸性水解酶降解。脂噬作用从 TGs 分解产生的游离脂肪酸为细胞线粒体 β-氧化提供燃料。因此,脂噬作用可调节细胞内脂质储存、细胞内游离脂质(如脂肪酸)水平和能量稳态。脂噬作用代谢的脂质量会根据外源性营养物质的供应而变化。细胞根据营养状况改变靶向自噬降解的脂质量的能力表明,该过程是有选择性的。细胞内脂质本身通过不明确的机制调节自噬水平。脂噬作用受损可导致组织内脂质过度积累,如肝脂肪变性,改变下丘脑神经肽的释放以影响体重,阻止细胞转分化,并使细胞对死亡刺激敏感。未来的研究可能会确定脂噬作用调节细胞生理学的其他机制,使该途径成为多种疾病的潜在治疗靶点。