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A Plasma Protein Network Regulates PM20D1 and N-Acyl Amino Acid Bioactivity.血浆蛋白网络调节PM20D1和N-酰基氨基酸的生物活性。
Cell Chem Biol. 2020 Sep 17;27(9):1130-1139.e4. doi: 10.1016/j.chembiol.2020.04.009. Epub 2020 May 12.
2
Cooperative enzymatic control of N-acyl amino acids by PM20D1 and FAAH.PM20D1 和 FAAH 对 N-酰基氨基酸的协同酶控作用。
Elife. 2020 Apr 9;9:e55211. doi: 10.7554/eLife.55211.
3
AIG1 and ADTRP are endogenous hydrolases of fatty acid esters of hydroxy fatty acids (FAHFAs) in mice.AIG1 和 ADTRP 是小鼠中羟脂肪酸酯(FAHFAs)的脂肪酸酯的内源性水解酶。
J Biol Chem. 2020 May 1;295(18):5891-5905. doi: 10.1074/jbc.RA119.012145. Epub 2020 Mar 9.
4
Natural human genetic variation determines basal and inducible expression of , an obesity-associated gene.天然人类遗传变异决定了肥胖相关基因 的基础表达和诱导表达。
Proc Natl Acad Sci U S A. 2019 Nov 12;116(46):23232-23242. doi: 10.1073/pnas.1913199116. Epub 2019 Oct 28.
5
PAHSAs enhance hepatic and systemic insulin sensitivity through direct and indirect mechanisms.PAHSAs 通过直接和间接机制增强肝脏和全身胰岛素敏感性。
J Clin Invest. 2019 Oct 1;129(10):4138-4150. doi: 10.1172/JCI127092.
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PAHSAs attenuate immune responses and promote β cell survival in autoimmune diabetic mice.PAHSAs 可减弱自身免疫性糖尿病小鼠的免疫反应并促进β细胞存活。
J Clin Invest. 2019 Aug 5;129(9):3717-3731. doi: 10.1172/JCI122445.
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12-Lipoxygenase Regulates Cold Adaptation and Glucose Metabolism by Producing the Omega-3 Lipid 12-HEPE from Brown Fat.12-脂氧合酶通过棕色脂肪产生 omega-3 脂质 12-HEPE 来调节冷适应和葡萄糖代谢。
Cell Metab. 2019 Oct 1;30(4):768-783.e7. doi: 10.1016/j.cmet.2019.07.001. Epub 2019 Jul 25.
8
The endocrine function of adipose tissues in health and cardiometabolic disease.健康与心血管代谢疾病中的脂肪组织内分泌功能。
Nat Rev Endocrinol. 2019 Sep;15(9):507-524. doi: 10.1038/s41574-019-0230-6. Epub 2019 Jul 11.
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A PRDM16-Driven Metabolic Signal from Adipocytes Regulates Precursor Cell Fate.脂肪细胞中的 PRDM16 驱动代谢信号调节前体细胞命运。
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Adipose-derived autotaxin regulates inflammation and steatosis associated with diet-induced obesity.脂肪来源的自分泌运动因子调节与饮食诱导肥胖相关的炎症和脂肪变性。
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脂肪组织脂素:最新进展与未来方向。

Adipose Tissue Lipokines: Recent Progress and Future Directions.

机构信息

Department of Pathology, Stanford University School of Medicine, Stanford, CA.

Stanford ChEM-H, Stanford University, Stanford, CA.

出版信息

Diabetes. 2020 Dec;69(12):2541-2548. doi: 10.2337/dbi20-0012.

DOI:10.2337/dbi20-0012
PMID:33219098
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7679773/
Abstract

Beyond classical metabolic functions in energy storage and energy expenditure, adipose tissue is also a dynamic endocrine organ that secretes bioactive factors into blood plasma. Historically, studies of the adipose secretome have predominantly focused on polypeptide adipokines. Recently, adipose-derived blood-borne lipids ("lipokines") have emerged as a distinct class of endocrine factors. Lipokines are intimately connected to intracellular pathways of fatty acid metabolism and therefore uniquely poised to communicate the intracellular energy status of adipocytes to other nonadipose tissues including liver, muscle, and pancreas. Here, we discuss recent progress on our understanding of adipose-secreted lipokines as endocrine regulators of glucose and lipid metabolism. We also provide our perspective on future directions for adipose-secreted lipids, including limitations of the currently available experimental data as well as potential strategies for addressing the remaining open questions.

摘要

除了在能量储存和能量消耗方面的经典代谢功能外,脂肪组织还是一种具有分泌生物活性因子到血浆功能的动态内分泌器官。从历史上看,对脂肪分泌组的研究主要集中在多肽脂肪因子上。最近,脂肪衍生的血液源性脂质(“脂因子”)已成为一类独特的内分泌因子。脂因子与脂肪酸代谢的细胞内途径密切相关,因此能够将脂肪细胞的细胞内能量状态独特地传递给其他非脂肪组织,包括肝脏、肌肉和胰腺。在这里,我们讨论了我们对脂肪分泌的脂因子作为葡萄糖和脂质代谢的内分泌调节剂的最新理解。我们还提供了对未来脂肪分泌脂质的展望,包括当前可用实验数据的局限性以及解决剩余未解决问题的潜在策略。