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Regulation of macrophage migration in ischemic mouse hearts via an AKT2/NBA1/SPK1 pathway

  • Yanping Yang
  • , Jieqiong Zhao
  • , Juan Zhang
  • , Yonghong Lei
  • , Fang Yuan
  • , Lu Liu
  • , Haibo Gao
  • , Hua Guo
  • , Xiaolin Niu
  • , Ruirui Chen
  • , Xiaobing Fu
  • , Yan Han
  • , Hua Han
  • , Tung Chan
  • , Lianyou Zhao
  • , Haichang Wang
  • , Qiangsun Zheng
  • , Xue Li
  • Tangdu Hospital, Fourth Military Medical University
  • General Hospital of People's Liberation Army
  • Chinese General Hospital
  • Air Force Medical University
  • Xibei Hospital

科研成果: 期刊稿件文章同行评审

2 引用 (Scopus)

摘要

The role of the AKT2/NBA1/SPK1 signaling cascade in macrophage migration regulation and post-ischemic cardiac remodeling was investigated. We determined that the AKT2/NBA1/SPK1 signaling cascade regulated macrophage migration. A novel role for NBA1 in macrophage migration was discovered. Elevated AKT2 phosphorylation, NBA1, SPK1 (along with phosphorylated SPK1) levels, macrophage recruitment, apoptosis, and fibrosis were found within the infarct area. Atorvastatin had a beneficial effect on cardiac remodeling following myocardial infarction by inhibiting AKT2/NBA1/SPK1-mediated macrophage recruitment, apoptosis, and collagen deposition while increasing angiogenesis in the infarct area. Atorvastatin-related protection of cardiac remodeling following myocardial infarction was abolished in SPK1-KO mice. The AKT2/NAB1/SPK1 pathway is a novel regulating factor of macrophage migration and cardiac remodeling after myocardial infarction.

源语言英语
页(从-至)115345-115359
页数15
期刊Oncotarget
8
70
DOI
出版状态已出版 - 2017
已对外发布

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