转分化
梅尔特克
肺纤维化
基因敲除
纤维化
癌症研究
信号转导
医学
粒体自噬
基因剔除小鼠
特发性肺纤维化
细胞生物学
生物
功能(生物学)
体外
免疫学
肺功能测试
表型
机制(生物学)
肺
背景(考古学)
转基因小鼠
肌成纤维细胞
病理
条件基因敲除
化学
细胞信号
作者
Yungeng Wei,Guo H,Xiangsheng Yang,Xiao Xiao Tang
摘要
In recent years, macrophage-to-myofibroblast transdifferentiation (MMT) has been found in fibrosis-related diseases. We confirmed the presence of MMT in human idiopathic pulmonary fibrosis (IPF) lungs and bleomycin-induced murine model using immunological and molecular methods. Mechanistically, ligand (GAS6)-mediated activation of MERTK on macrophages initiates a sequential signaling cascade involving SPP1, SRC, and TKS5, which collectively drives the transdifferentiation program. Conversely, knockout of MERTK specifically in macrophages or adeno-associated virus (AAV)-mediated knockdown of TKS5 effectively disrupted this MERTK-SPP1-SRC-TKS5 axis, potently suppressing MMT in vitro and in vivo. These interventions significantly attenuated the progression of pulmonary fibrosis, as evidenced by comprehensive assessments including microCT, pulmonary function test, and histopathological analysis. Our findings establish MMT as a key pathogenic mechanism and identify the MERTK-initiated signaling axis as a novel therapeutic target.
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