Novel insights into the biological function of mast cell carboxypeptidase A

Trends Immunol. 2009 Aug;30(8):401-8. doi: 10.1016/j.it.2009.04.008. Epub 2009 Jul 28.

Abstract

When mast cells are activated they can respond by releasing their secretory granule compounds, including mast cell-specific proteases of chymase, tryptase and carboxypeptidase A (MC-CPA) type. MC-CPA is a dominant protein component of the mast cell granule and the MC-CPA gene is extremely highly expressed. Despite this, relatively little has been known of its biological function. However, the recent generation of mouse strains lacking MC-CPA has opened up new possibilities for investigations related to this protease. This recent development has revealed a role for MC-CPA in regulating innate immunity responses, including the degradation of harmful substances such as the vasoconstrictive factor endothelin 1 and snake venom toxins. Here, we summarize the current knowledge of MC-CPA.

Publication types

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

MeSH terms

  • Animals
  • Carboxypeptidases A* / chemistry
  • Carboxypeptidases A* / genetics
  • Carboxypeptidases A* / metabolism
  • Carboxypeptidases A* / physiology
  • Humans
  • Immunity, Innate / physiology*
  • Mast Cells / enzymology*
  • Mice
  • Rats
  • Secretory Vesicles / metabolism*
  • Substrate Specificity

Substances

  • Carboxypeptidases A