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肠道上皮细胞来源的外泌体在肠-肝芯片模型中促进肝祖细胞的肝向分化。

Exosomes From Intestinal Epithelial Cells Promote Hepatic Differentiation of Liver Progenitor Cells in Gut-Liver-on-a-Chip Models.

作者信息

Ye Liang, Li Shi, Bi Guofang, Li Binghui, Cai Zhai, Jin Meixian, Zhang Ying, Yang Wanren, Li Yang, Li Shao, Hu Wei, Gao Yi, Pan Mingxin, Zhou Shuqin, Zhang Chao, Bi Huichang, Peng Qing

机构信息

Department of Hepatobiliary Surgery II, General Surgery Center, Zhujiang Hospital, Southern Medical University, Guangzhou, Guangdong, 510282, China.

Central Laboratory of the Second Affiliated Hospital, School of Medicine, The Chinese University of Hong Kong, Shenzhen & Longgang District People's Hospital of Shenzhen, Shenzhen, 510282, China.

出版信息

Adv Sci (Weinh). 2025 Aug;12(32):e17478. doi: 10.1002/advs.202417478. Epub 2025 Jul 6.

Abstract

Hepatic progenitor cells (HPCs) are frequently overactivated, and their differentiation into hepatocytes is impaired in advanced liver diseases. To explore the effects of intestinal epithelial cells and their exosomes on the hepatic differentiation of HPCs, co-culture systems of Caco-2/HepaRG cell lines and intestine/HPC organoids are established in a novel gut-liver-on-a-chip. Exosomes derived from intestinal organoids are administered to mice with carbon tetrachloride (CCL4)-induced liver fibrosis. The results showed that the co-culture of HPCs and intestinal epithelial cells promoted the hepatic differentiation of HPCs, mediated by exosomes derived from intestinal epithelial cells. Treatment with exosomes derived from intestinal organoids ameliorated liver fibrosis in a mouse model of CCL4-induced liver fibrosis. A cluster of miRNAs, miR-371-373, is identified within the exosomes of the intestinal epithelial cells, which target RPS6KA2 to modulate hepatic differentiation. This findings demonstrate that exosomes from intestinal epithelial cells promote the hepatic differentiation of HPCs. Exosomes from intestinal organoids may be a novel therapeutic strategy for the treatment of advanced liver diseases.

摘要

肝祖细胞(HPCs)常常过度激活,在晚期肝病中其向肝细胞的分化受损。为探究肠上皮细胞及其外泌体对HPCs肝分化的影响,在一种新型的肠道-肝脏芯片中建立了Caco-2/HepaRG细胞系和肠/HPC类器官的共培养体系。将源自肠类器官的外泌体给予四氯化碳(CCL4)诱导肝纤维化的小鼠。结果表明,HPCs与肠上皮细胞的共培养促进了HPCs的肝分化,这由源自肠上皮细胞的外泌体介导。用源自肠类器官的外泌体治疗可改善CCL4诱导的肝纤维化小鼠模型中的肝纤维化。在肠上皮细胞的外泌体内鉴定出一簇微小RNA,即miR-371-373,其靶向RPS6KA2以调节肝分化。这些发现表明,来自肠上皮细胞的外泌体促进了HPCs的肝分化。来自肠类器官的外泌体可能是治疗晚期肝病的一种新型治疗策略。

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