祖细胞
类有机物
微泡
肠上皮
肝星状细胞
细胞分化
细胞生物学
癌症研究
生物
干细胞
上皮
医学
病理
生物化学
内分泌学
小RNA
基因
作者
Liang Ye,Li Shi,Guofang Bi,Binghui Li,Zhai Cai,Meixian Jin,Ying Zhang,Wanren Yang,Yang Li,Shao Li,Wei Hu,Yi Gao,Mingxin Pan,Shuqin Zhou,Chao Zhang,Guofang Bi,Qing Peng
标识
DOI:10.1002/advs.202417478
摘要
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.
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