The activation of mTOR is required for monocyte pro-inflammatory response in patients with coronary artery disease

Shanshan Gao1, Weimin Liu1, Xiaozhen Zhuo1

  • 1*Department of Cardiology, First Affiliated Hospital of Xi'an Jiaotong University, Shaanxi Xi'an 710061, China.

Insights

Mammalian target of rapamycin (mTOR) activation drives inflammation in coronary artery disease (CAD) by enhancing nuclear factor-κB (NF-κB) signalling in human monocytes. Inhibiting mTOR may offer new strategies to treat atherosclerosis.

Area of Science:

  • Cardiovascular Biology
  • Inflammation Research
  • Molecular Medicine

Background:

  • Nuclear factor-κB (NF-κB) is central to inflammation in atherosclerosis (AS).
  • Mammalian target of rapamycin (mTOR) is implicated in chronic inflammation.
  • The interplay between mTOR and NF-κB in AS remains unclear.

Purpose of the Study:

  • Investigate mTOR's role in the pro-inflammatory pathway of human monocytes (HMCs) in coronary artery disease (CAD).
  • Determine the interaction between mTOR and NF-κB signalling in the inflammatory state of CAD.

Main Methods:

  • Isolated HMCs from CAD patients and non-CAD controls.
  • Assessed NF-κB activity, p65 nuclear translocation, and mTOR phosphorylation.
  • Utilized an in vitro model with HMCs treated with CAD or control sera.
  • Employed pharmacological and genetic inhibition of mTOR.
  • Evaluated the effect of statins.

Main Results:

  • CAD patients exhibited elevated NF-κB activity, p65 translocation, and mTOR phosphorylation compared to controls.
  • Serum from CAD patients induced mTOR phosphorylation, NF-κB activation, and inflammation in HMCs.
  • mTOR inhibition abrogated CAD serum-induced NF-κB activation and inflammation.
  • Statins partially inhibited mTOR activation and pro-inflammatory responses.

Conclusions:

  • CAD patients present a pro-inflammatory state characterized by increased NF-κB and mTOR activity.
  • mTOR activation is essential for the NF-κB-dependent pro-inflammatory response in HMCs.
  • This highlights a potential therapeutic target for attenuating AS.