特发性肺纤维化
肺纤维化
发病机制
癌症研究
癌基因
细胞
巨噬细胞极化
巨噬细胞
细胞周期
纤维化
磷蛋白
生物
免疫学
肺
信号转导
医学
病理
磷酸化
细胞生物学
内科学
体外
生物化学
遗传学
作者
Xuelian Yang,Ziqin Liu,Jiawei Zhou,Jianqiang Guo,Tao Han,Yafeng Liu,Yunyun Li,Ying Bai,Yingru Xing,Jing Wu,Dong Hu
标识
DOI:10.3892/ijmm.2024.5413
摘要
Idiopathic pulmonary fibrosis (IPF) is a fatal pulmonary disease that requires further investigation to understand its pathogenesis. The present study demonstrated that secreted phosphoprotein 1 (SPP1) was aberrantly highly expressed in the lung tissue of patients with IPF and was significantly positively associated with macrophage and T‑cell activity. Cell localization studies revealed that SPP1 was primarily overexpressed in macrophages, rather than in T cells. Functionally, knocking down SPP1 expression
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