基因敲除
SMAD公司
间充质干细胞
癌症研究
肺动脉高压
肺动脉
内皮干细胞
医学
生物
病理
转化生长因子
内科学
细胞培养
生物化学
遗传学
体外
作者
Qiuhong Jiao,Xiufeng Xu,Longwu Xu,Yuying Wang,Shulan Pang,Jie Hao,Xiaohong Liu,Yudan Zhao,Wanpeng Qi,Limin Qin,Tao Huang,Jingtian Li,Tao Wang
标识
DOI:10.1186/s12967-025-06505-3
摘要
Knockdown of eIF3a inhibited EndMT in PAECs regulating TGFβ1/SMAD signaling pathway, significantly alleviated the changes of RVSP, RVH and vascular remodeling in MCT-induced PAH rats, eIF3a may be a promising and novel therapeutic target for the treatment of PAH.
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