Jiang Xinru, Zhao Wei, Shen Botao, Han Yumeng, Chen Kexin
Department of Cardiology, The First Hospital of Jilin University, Changchun, China.
Core Facility of the First Hospital of Jilin University, Changchun, China.
Front Endocrinol (Lausanne). 2025 Jun 24;16:1535382. doi: 10.3389/fendo.2025.1535382. eCollection 2025.
Metabolic dysfunction-associated steatotic liver disease (MASLD), previously known as non-alcoholic fatty liver disease (NAFLD), has gradually become a leading cause of end-stage liver disease as a heterogeneous group of diseases. While the underlying mechanisms of MASLD remain incompletely understood, it is clear that glycolipid metabolism, coupled with subsequent disruptions in hepatic sinusoidal homeostasis and cellular senescence play significant roles in its onset and progression. In recent years, CD47 has been recognized not only as a critical target in cancer therapy but also as a participant in the development of metabolic diseases through complex signaling pathways. Increasing evidence suggests that CD47 is closely associated with the development of MASLD; however, its role in MASLD has not yet been widely explored. Therefore, this review aims to summarize current research on the potential role of CD47 in the pathogenesis of MASLD, particularly in relation to disturbances in glucose and lipid metabolism.
代谢功能障碍相关脂肪性肝病(MASLD),以前称为非酒精性脂肪性肝病(NAFLD),作为一组异质性疾病,已逐渐成为终末期肝病的主要原因。虽然MASLD的潜在机制仍未完全了解,但很明显,糖脂代谢以及随后肝窦稳态和细胞衰老的破坏在其发病和进展中起重要作用。近年来,CD47不仅被认为是癌症治疗的关键靶点,还通过复杂的信号通路参与代谢性疾病的发展。越来越多的证据表明,CD47与MASLD的发展密切相关;然而,其在MASLD中的作用尚未得到广泛研究。因此,本综述旨在总结目前关于CD47在MASLD发病机制中潜在作用的研究,特别是与糖脂代谢紊乱相关的研究。