CD36在肝脏疾病中的作用

IF 5.6 2区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Hepatology Communications Pub Date : 2025-01-07 eCollection Date: 2025-01-01 DOI:10.1097/HC9.0000000000000623
Yi Liu, Wenwei Yin
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引用次数: 0

摘要

CD36是一种跨膜糖蛋白,能够结合多种配体并发挥多种功能。CD36通过识别长链脂肪酸、含有血栓spondin结构同源重复结构域的蛋白(如thrombospondin-1)以及分子结构与危险或病原体相关分子模式一致的分子,参与机体的各种生理和病理过程。CD36广泛表达于各种细胞类型,包括肝细胞和肝细胞,在脂质代谢、炎症和氧化应激中起关键作用。越来越多的证据表明,CD36在非酒精性单纯性脂肪性肝病和NASH的发展中起着复杂的作用,并参与炎症性肝损伤、乙型/丙型肝炎、肝纤维化和肝癌的发病机制。本文综述了目前在肝脏病理生理背景下对CD36的结构特性、表达模式和功能机制的理解。此外,CD36作为预防和治疗肝脏疾病的治疗靶点的潜力也得到了强调。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
CD36 in liver diseases.

Cluster of differentiation 36 (CD36) is a transmembrane glycoprotein with the ability to bind to multiple ligands and perform diverse functions. Through the recognition of long-chain fatty acids, proteins containing thrombospondin structural homology repeat domains such as thrombospondin-1, and molecules with molecular structures consistent with danger- or pathogen-associated molecular patterns, CD36 participates in various physiological and pathological processes of the body. CD36 is widely expressed in various cell types, including hepatocytes and KCs in the liver, where it plays a pivotal role in lipid metabolism, inflammation, and oxidative stress. Accumulating evidence suggests that CD36 plays a complex role in the development of nonalcoholic simple fatty liver disease and NASH and contributes to the pathogenesis of inflammatory liver injury, hepatitis B/hepatitis C, liver fibrosis, and liver cancer. This review summarizes the current understanding of the structural properties, expression patterns, and functional mechanisms of CD36 in the context of liver pathophysiology. Furthermore, the potential of CD36 as a therapeutic target for the prevention and treatment of liver diseases is highlighted.

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来源期刊
Hepatology Communications
Hepatology Communications GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
8.00
自引率
2.00%
发文量
248
审稿时长
8 weeks
期刊介绍: Hepatology Communications is a peer-reviewed, online-only, open access journal for fast dissemination of high quality basic, translational, and clinical research in hepatology. Hepatology Communications maintains high standard and rigorous peer review. Because of its open access nature, authors retain the copyright to their works, all articles are immediately available and free to read and share, and it is fully compliant with funder and institutional mandates. The journal is committed to fast publication and author satisfaction. ​
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