Protease-activated receptors: novel PARtners in innate immunity

Trends Immunol. 2007 Dec;28(12):541-50. doi: 10.1016/j.it.2007.09.001. Epub 2007 Oct 30.

Abstract

Protease-activated receptors (PARs) belong to a family of G protein-coupled receptors activated by serine proteases via proteolytic cleavage. PARs are expressed on epithelial cells, endothelial cells, and leukocytes, indicating a role in controlling barrier function against external danger. During inflammation, microorganisms as well as host immune cells release various proteases activating PARs. Thus, PARs can be viewed as an integral component of the host antimicrobial alarm system. When stimulated, PARs regulate various functions of leukocytes in vivo and in vitro, revealing a novel pathway by which proteases affect innate immune responses. Understanding protease-immune interactions could lead to novel strategies for the treatment of infectious and immune-related diseases.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Cathepsin G
  • Cathepsins / physiology
  • Dendritic Cells / physiology
  • Granzymes / physiology
  • Humans
  • Immunity, Innate*
  • Macrophages / physiology
  • Mast Cells / physiology
  • Monocytes / physiology
  • Neutrophils / physiology
  • Receptors, Proteinase-Activated / physiology*
  • Serine Endopeptidases / physiology
  • Tryptases / physiology

Substances

  • Receptors, Proteinase-Activated
  • Cathepsins
  • Granzymes
  • Serine Endopeptidases
  • CTSG protein, human
  • Cathepsin G
  • Tryptases