阿格里坎
软骨细胞
PI3K/AKT/mTOR通路
蛋白激酶B
化学
磷酸化
LY294002型
II型胶原
细胞生物学
细胞外基质
免疫印迹
医学
信号转导
分子生物学
软骨
生物
生物化学
解剖
病理
基因
骨关节炎
体外
替代医学
关节软骨
作者
Xia Chen,Ruhong Zhang,Qun Zhang,Zhicheng Xu,Feng Xu,Datao Li,Yiyuan Li
摘要
Abstract Objective To explore the effectiveness of the insulin‐like growth factor 1 receptor (IGF‐1R)/PI3K/AKT pathway in promoting the synthesis of the auricular chondrocyte extracellular matrix (ECM) using concentrated growth factor (CGF). Methods Chondrocytes isolated from the remnant auricular cartilage of microtia patients were randomly divided into different experimental and control groups, then stimulated with a reagent. IGF‐1 released by CGF was quantified by enzyme‐linked immunosorbent assay. Glycosaminoglycan (GAG), proteoglycan, and type II collagen (COLAII) were examined by histological and immunohistological analysis. Expression levels of IGF‐1R, pIGF‐1R, PI3K, pPI3K, AKT, pAKT, COLAII, and Aggrecan were detected by western blot analysis technique and gene expression was tested by real‐time polymerase chain reaction. Results CGF significantly stimulated the synthesis of COLAII and Aggrecan and increased the phosphorylation levels of IGF‐1R, PI3K, and AKT. Small interfering RNA IGF‐1 blocked ECM synthesis, COLAII and Aggrecan gene expression, and IGF‐1R/PI3K/AKT activation. Inhibitor AG1024 and LY294002 significantly inhibited ECM synthesis and the phosphorylation of IGF‐1R, PI3K, and AKT. Conclusion CGF‐released IGF‐1 stimulates the synthesis of the auricular chondrocyte ECM via the IGF‐1R/PI3K/AKT signaling pathway.
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