PTEN公司
原癌基因酪氨酸蛋白激酶Src
蛋白激酶B
磷酸化
化学
PI3K/AKT/mTOR通路
神经炎症
信号转导
癌症研究
药理学
细胞生物学
生物化学
生物
炎症
免疫学
作者
Fangfang Li,Yang Zheng,Gen Li,Yang Yang,Jingwei Ma,Caixia Zang,Tao Deng,Li Li,Xiu‐Qi Bao,D. Zhang
标识
DOI:10.1080/10286020.2024.2435981
摘要
Compound FLZ has neuroprotective effects on Parkinson's disease (PD), while the precise mechanism remains unclear. In this study, we found that FLZ decreased PTEN/Akt activity in LPS-challenged BV2 cells. Neuroinflammatory responses suppressed by FLZ were abolished when PTEN or Src was inhibited. Additionally, FLZ weakened the interactions of Src and PTEN, and attenuated Src phosphorylation once PETN was inhibited, but failed to decrease PTEN phosphorylation when Src was silenced. Eventually, we elaborated that FLZ bound to Src directly and inhibited its activity. Collectively, FLZ attenuated neuroinflammation through inhibiting Src/PTEN/Akt pathway, paving the way for clinical use of FLZ to treat PD.
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