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血管生成素样蛋白4——脂质代谢与炎症的联系纽带

ANGPTL4-the Link Binding Lipid Metabolism and Inflammation.

作者信息

Zhang Yueqi, Liang Jingwen, Li Zhi, Zuo Yuyue, Dai Lei

机构信息

Division of Cardiology, Department of Internal Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, Hubei, China.

Hubei Provincial Engineering Research Center of Vascular Interventional Therapy, Wuhan, 430030, Hubei, China.

出版信息

Curr Med Chem. 2025;32(15):2931-2949. doi: 10.2174/0109298673320024240829070906.

Abstract

BACKGROUND

Angiopoietin-like 4 (ANGPTL4) belongs to the family of angiopoietin- like proteins. The involvement of ANGPTL4 in various aspects of lipid metabolism and inflammation has become an important area of research.

METHODS

A thorough search on PubMed related to ANGPTL4, lipid metabolism, and inflammation was performed.

RESULTS

Over the past two decades, the recognition of ANGPTL4 as a potent regulator of lipid metabolism has substantially increased. As part of the senescence-associated secretory phenotype, ANGPTL4 also serves as an inflammatory mediator. Considering the advancements in ANGPTL4 research, we have highlighted that ANGPTL4 acts as a key node linking lipid metabolism and inflammation. ANGPTL4 impacts inflammation by regulating lipid metabolism. It affects critical enzymes (lipoprotein lipase, hepatic lipase, endothelial lipase, and acetyl-CoA carboxylase), regulatory factors (AMPK, cAMP, SLC7A11, GPX4, and mTOR), and receptors (LepR, CD36, and PPARγ) of lipid oxidation, synthesis, and peroxidation, thereby affecting immune cells and inflammatory pathways.

CONCLUSION

Understanding the potential association and the therapeutic value of ANGPTL4 for regulating lipid metabolism and inflammation could contribute to drug discovery and therapeutic development.

摘要

背景

血管生成素样4(ANGPTL4)属于血管生成素样蛋白家族。ANGPTL4参与脂质代谢和炎症的各个方面已成为一个重要的研究领域。

方法

对PubMed上与ANGPTL4、脂质代谢和炎症相关的文献进行了全面检索。

结果

在过去二十年中,ANGPTL4作为脂质代谢有效调节因子的认知大幅增加。作为衰老相关分泌表型的一部分,ANGPTL4还作为一种炎症介质。考虑到ANGPTL4研究的进展,我们强调ANGPTL4是连接脂质代谢和炎症的关键节点。ANGPTL4通过调节脂质代谢影响炎症。它影响脂质氧化、合成和过氧化的关键酶(脂蛋白脂肪酶、肝脂肪酶、内皮脂肪酶和乙酰辅酶A羧化酶)、调节因子(AMPK、cAMP、SLC7A11、GPX4和mTOR)以及受体(LepR、CD36和PPARγ),从而影响免疫细胞和炎症途径。

结论

了解ANGPTL4在调节脂质代谢和炎症方面的潜在关联及治疗价值,可能有助于药物发现和治疗开发。

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