串扰
胰岛素受体
胰高血糖素样肽1受体
受体
细胞生物学
信号转导
胰岛素受体底物
细胞信号
化学
胰岛素
细胞内
生物
生物化学
内分泌学
胰岛素抵抗
兴奋剂
物理
光学
作者
Yubo Wang,Xinyu Song,Yan Wang,Nan Wang
标识
DOI:10.1016/j.bbrc.2022.10.094
摘要
Both GLP-1 receptor (GLP-1R) and insulin receptor (IR) transmit signals for insulin release and/or cellular metabolism although using distinct sets of transducing molecules and separate pathways. We proposed a possible association of IR and GLP-1R, since they are coexpressed in diverse tissues including the pancreatic β-cells and crosstalk between their signaling was frequently reported. We showed a specific interaction between GLP-1R and IR which was independent of intracellular receptor domains and not responsive to ligand binding. In signaling, the IRS-1 was coupled more to GLP-1R and less to IR in the receptor complex at IR activation, with subsequent IRS-1 degradation suppressed rather than its activation inhibited. The Gsα recruitment to the activated GLP-1R was inhibited in the GLP-1R/IR complex, with the signaling in cAMP pathway suppressed at IR activation. Therefore, the identified GLP-1R/IR complex recruits their signaling molecules which are differentially modified, leading to a crosstalk between their signaling.
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