Mast cells can secrete vascular permeability factor/vascular endothelial cell growth factor and exhibit enhanced release after immunoglobulin E–dependent …

J Boesiger, M Tsai, M Maurer, M Yamaguchi… - The Journal of …, 1998 - rupress.org
J Boesiger, M Tsai, M Maurer, M Yamaguchi, LF Brown, KP Claffey, HF Dvorak, SJ Galli
The Journal of experimental medicine, 1998rupress.org
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 …
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.
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