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
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Boesiger, J
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机构:Beth Israel Deaconess Med Ctr E, Dept Pathol, Boston, MA 02215 USA
Boesiger, J
Tsai, M
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机构:Beth Israel Deaconess Med Ctr E, Dept Pathol, Boston, MA 02215 USA
Tsai, M
Maurer, M
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机构:Beth Israel Deaconess Med Ctr E, Dept Pathol, Boston, MA 02215 USA
Maurer, M
Yamaguchi, M
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机构:Beth Israel Deaconess Med Ctr E, Dept Pathol, Boston, MA 02215 USA
Yamaguchi, M
Brown, LF
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机构:Beth Israel Deaconess Med Ctr E, Dept Pathol, Boston, MA 02215 USA
Brown, LF
Claffey, KP
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机构:Beth Israel Deaconess Med Ctr E, Dept Pathol, Boston, MA 02215 USA
Claffey, KP
Dvorak, HF
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机构:Beth Israel Deaconess Med Ctr E, Dept Pathol, Boston, MA 02215 USA
Dvorak, HF
Galli, SJ
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机构:Beth Israel Deaconess Med Ctr E, Dept Pathol, Boston, MA 02215 USA
Galli, SJ
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[1] Beth Israel Deaconess Med Ctr E, Dept Pathol, Boston, MA 02215 USA
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 Fc epsilon receptor I (Fc epsilon RI) 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 Fc epsilon RI-dependent secretion of VPF/VEGF by either mouse or human mast cells can be significantly increased in cells which have undergone upregulation of Fc epsilon RI surface expression by a 4-d preincubation with immunoglobulin E. These finding; 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.