Gut Microbial Metabolite TMAO Enhances Platelet Hyperreactivity and Thrombosis Risk

Cell. 2016 Mar 24;165(1):111-124. doi: 10.1016/j.cell.2016.02.011. Epub 2016 Mar 10.

Abstract

Normal platelet function is critical to blood hemostasis and maintenance of a closed circulatory system. Heightened platelet reactivity, however, is associated with cardiometabolic diseases and enhanced potential for thrombotic events. We now show gut microbes, through generation of trimethylamine N-oxide (TMAO), directly contribute to platelet hyperreactivity and enhanced thrombosis potential. Plasma TMAO levels in subjects (n > 4,000) independently predicted incident (3 years) thrombosis (heart attack, stroke) risk. Direct exposure of platelets to TMAO enhanced sub-maximal stimulus-dependent platelet activation from multiple agonists through augmented Ca(2+) release from intracellular stores. Animal model studies employing dietary choline or TMAO, germ-free mice, and microbial transplantation collectively confirm a role for gut microbiota and TMAO in modulating platelet hyperresponsiveness and thrombosis potential and identify microbial taxa associated with plasma TMAO and thrombosis potential. Collectively, the present results reveal a previously unrecognized mechanistic link between specific dietary nutrients, gut microbes, platelet function, and thrombosis risk.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood Platelets / metabolism*
  • Calcium / metabolism
  • Carotid Artery Injuries / pathology
  • Cecum / microbiology
  • Chlorides
  • Choline / metabolism
  • Diet
  • Female
  • Ferric Compounds
  • Gastrointestinal Microbiome*
  • Germ-Free Life
  • Humans
  • Methylamines / blood
  • Methylamines / metabolism*
  • Mice
  • Mice, Inbred C57BL
  • Thrombosis / metabolism*
  • Thrombosis / pathology

Substances

  • Chlorides
  • Ferric Compounds
  • Methylamines
  • trimethyloxamine
  • Choline
  • Calcium
  • ferric chloride