Mast cells can secrete vascular permeability factor/vascular endothelial cell growth factor and exhibit enhanced release after immunoglobulin E- dependent upregulation of Fcε receptor I expression

Jürg Boesiger, Mindy Tsai, Marcus Maurer, Masao Yamaguchi, Lawrence F. Brown, Kevin P. Claffey, Harold F. Dvorak, Stephen J. Galli

Research output: Contribution to journalArticlepeer-review

315 Scopus citations

Abstract

Vascular permeability factor/vascular endothelial cell growth factor (VPF/VEGF) can both potently enhance vascular permeability and induce proliferation of vascular endothelial cells. We report here that mouse or human mast cells can produce and secrete VPF/VEGF. Mouse mast cells release VPF/VEGF upon stimulation through Fcε receptor I (FcεRI) or c-kit, or after challenge with the protein kinase C activator, phorbol myristate acetate, or the calcium ionophore, A23187; such mast cells can rapidly release VPF/VEGF, apparently from a preformed pool, and can then sustain release by secreting newly synthesized protein. Notably, the FcεRI-dependent secretion of VPF/VEGF by either mouse or human mast cells can be significantly increased in cells which have undergone upregulation of FcεRI surface expression by a 4-d preincubation with immunoglobulin E. These findings establish that at least one cell type, the mast cell, can be stimulated to secrete VPF/VEGF upon immunologically specific activation via a member of the multichain immune recognition receptor family. Our observations also identify a new mechanism by which mast cells can contribute to enhanced vascular permeability and/or angiogenesis, in both allergic diseases and other settings.

Original languageEnglish
Pages (from-to)1135-1145
Number of pages11
JournalJournal of Experimental Medicine
Volume188
Issue number6
DOIs
StatePublished - 21 Sep 1998
Externally publishedYes

Keywords

  • Allergy
  • Angiogenesis
  • C-kit
  • Stem cell factor
  • Vascular permeability

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