Ancient origin of mast cells

Biochem Biophys Res Commun. 2014 Aug 22;451(2):314-8. doi: 10.1016/j.bbrc.2014.07.124. Epub 2014 Aug 2.

Abstract

The sentinel roles of mammalian mast cells (MCs) in varied infections raised the question of their evolutionary origin. We discovered that the test cells in the sea squirt Ciona intestinalis morphologically and histochemically resembled cutaneous human MCs. Like the latter, C. intestinalis test cells stored histamine and varied heparin·serine protease complexes in their granules. Moreover, they exocytosed these preformed mediators when exposed to compound 48/80. In support of the histamine data, a C. intestinalis-derived cDNA was isolated that resembled that which encodes histidine decarboxylase in human MCs. Like heparin-expressing mammalian MCs, activated test cells produced prostaglandin D2 and contained cDNAs that encode a protein that resembles the synthase needed for its biosynthesis in human MCs. The accumulated morphological, histochemical, biochemical, and molecular biology data suggest that the test cells in C. intestinalis are the counterparts of mammalian MCs that reside in varied connective tissues. The accumulated data point to an ancient origin of MCs that predates the emergence of the chordates >500million years ago, well before the development of adaptive immunity. The remarkable conservation of MCs throughout evolution is consistent with their importance in innate immunity.

Keywords: Ciona intestinalis; Heparin; Histamine; Mast cell; Prostaglandin D(2); Serine protease.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Biological Evolution*
  • Ciona intestinalis / cytology*
  • Ciona intestinalis / genetics
  • Ciona intestinalis / physiology*
  • Cloning, Molecular
  • Evolution, Molecular
  • Female
  • Glycosaminoglycans / metabolism
  • Heparin / metabolism
  • Histamine Release
  • Histidine Decarboxylase / genetics
  • Histidine Decarboxylase / metabolism
  • Humans
  • Immunity, Innate
  • Intramolecular Oxidoreductases / genetics
  • Lipocalins / genetics
  • Mast Cells / immunology
  • Mast Cells / physiology*
  • Mast Cells / ultrastructure*
  • Molecular Sequence Data
  • Prostaglandin D2 / biosynthesis
  • Secretory Vesicles / physiology
  • Sequence Homology, Amino Acid
  • Serine Proteases / metabolism
  • Species Specificity

Substances

  • Glycosaminoglycans
  • Lipocalins
  • Heparin
  • Serine Proteases
  • Histidine Decarboxylase
  • Intramolecular Oxidoreductases
  • prostaglandin R2 D-isomerase
  • Prostaglandin D2

Associated data

  • GENBANK/EF125183