贾纳斯激酶
特发性肺纤维化
肺纤维化
STAT蛋白
成纤维细胞
自噬
车站3
医学
纤维化
Janus激酶2
信号转导
癌症研究
激活剂(遗传学)
药理学
肺
化学
生物
细胞生物学
病理
内科学
受体
细胞凋亡
体外
生物化学
作者
Xing Zhang,Jie Su,Jiacheng Lin,linling liu,Jiamin Wu,Wenli Yuan,Yibao Zhang,Qi Chen,Zi-jian Su,Guihua Xu,Mingna Sun,Yile Zhang,Xuan Chen,Wei Zhang
标识
DOI:10.1016/j.jep.2023.116633
摘要
Fu-Zheng-Tong-Luo (FZTL) formula is a Chinese herbal prescription which is used to treat idiopathic pulmonary fibrosis (IPF). We previously reported that the FZTL formula could improve IPF injury in rats; however, the mechanism remains unelucidated.To elucidate the effects and mechanisms of the FZTL formula on IPF.The bleomycin-induced pulmonary fibrosis rat model and transforming growth factor-β-induced lung fibroblast model were used. Histological changes and fibrosis formation were detected in the rat model after treatment with the FZTL formula. Furthermore, the effects of the FZTL formula on autophagy and lung fibroblast activation were determined. Moreover, the mechanism of FZTL was explored using transcriptomics analysis.We observed that FZTL alleviated IPF injury in rats and inhibited inflammatory responses and fibrosis formation in rats. Moreover, it promoted autophagy and inhibited lung fibroblast activation in vitro. Transcriptomics analysis revealed that FZTL regulates the Janus kinase 2 (JAK)/signal transducer and activator of the transcription 3 (STAT) signaling pathway. The JAK2/STAT3 signaling activator interleukin 6 inhibited the anti-fibroblast activation effect of the FZTL formula. Combined treatment with the JAK2 inhibitor (AZD1480) and autophagy inhibitor (3-methyladenine) did not enhance the antifibrotic effect of FZTL.The FZTL formula can inhibit IPF injury and lung fibroblast activation. Its effects are mediated via the JAK2/STAT3 signaling pathway. The FZTL formula may be a potential complementary therapy for pulmonary fibrosis.
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