Inorganic polyphosphate: a key modulator of inflammation

J Thromb Haemost. 2017 Feb;15(2):213-218. doi: 10.1111/jth.13580. Epub 2017 Jan 5.

Abstract

Inorganic polyphosphate (PolyP) is a molecule with prothrombotic and proinflammatory properties in blood. PolyP activates the NF-κB signaling pathway, increases the expression of cell surface adhesion molecules and disrupts the vascular barrier integrity of endothelial cells. PolyP-induced NF-κB activation and vascular hyperpermeability are regulated by the mammalian target of rapamycin complex-1 (mTORC1) and mTORC2 pathways, respectively. Through interaction with receptor for advanced glycation end products (RAGE) and P2Y1 receptors, PolyP dramatically amplifies the proinflammatory responses of nuclear proteins. Moreover, PolyP-mediated activation of the contact pathway results in activation of the kallikrein-kinin system, which either directly or in cross-talk with the complement system induces inflammation in both cellular and animal systems. Thus, polyP is a novel therapeutic target for the treatment of metabolic and acute/chronic proinflammatory diseases, including severe sepsis, diabetes, cardiovascular disease and cancer. In this review, we discuss recent findings on the inflammatory properties of polyP and propose a model to explain the molecular mechanism of proinflammatory effects of this molecule in different systems.

Keywords: blood coagulation; inflammation; platelets; polyphosphates; thrombosis.

Publication types

  • Review

MeSH terms

  • Animals
  • Blood Coagulation
  • Cardiovascular Diseases / metabolism
  • Escherichia coli / metabolism
  • Glycation End Products, Advanced / metabolism
  • HMGB1 Protein / metabolism
  • Histones / metabolism
  • Humans
  • Inflammation / metabolism*
  • Inflammation Mediators / metabolism
  • Mechanistic Target of Rapamycin Complex 1 / metabolism
  • Mechanistic Target of Rapamycin Complex 2 / metabolism
  • Mice
  • NF-kappa B / metabolism
  • Neoplasms / metabolism
  • Polyphosphates / chemistry*
  • Signal Transduction

Substances

  • Glycation End Products, Advanced
  • HMGB1 Protein
  • HMGB1 protein, human
  • Histones
  • Inflammation Mediators
  • NF-kappa B
  • Polyphosphates
  • Mechanistic Target of Rapamycin Complex 1
  • Mechanistic Target of Rapamycin Complex 2