Basic fibroblast growth factor increases expression of the αvβ3 integrin complex on human microvascular endothelial cells

NT Sepp, LJ Li, KH Lee, EJ Brown… - Journal of Investigative …, 1994 - Elsevier
NT Sepp, LJ Li, KH Lee, EJ Brown, SW Caughman, TJ Lawley, RA Swerlick
Journal of Investigative Dermatology, 1994Elsevier
Modulation of the expression of the α v β 3 complex on human dermal microvascular
endothelial cells (HDMEC) may be crucial in wound healing and angiogenesis. Therefore,
we examined the influence of basic fibroblast growth factor (bFGF), transforming growth
factor β, and interferon-γ (IFN-γ) on the expression of this complex. Stimulation of HDMEC
with bFGF increased cell surface expression of both α v and β 3 in a dose-and time-
dependent manner associated with the development of a spindled, elongated cell …
Modulation of the expression of the αvβ3 complex on human dermal microvascular endothelial cells (HDMEC) may be crucial in wound healing and angiogenesis. Therefore, we examined the influence of basic fibroblast growth factor (bFGF), transforming growth factor β, and interferon-γ (IFN-γ) on the expression of this complex. Stimulation of HDMEC with bFGF increased cell surface expression of both αv and β3 in a dose- and time-dependent manner associated with the development of a spindled, elongated cell morphology. Northern blot analysis of HDMEC stimulated with bFGF demonstrated a marked increase in β3 but not αv mRNA expression. Incubation of HDMEC with transforming growth factor-β or interferon-γ alone resulted in modest decreases in cell surface αvβ3, and co-incubation of HDMEC with bFGF and transforming growth factor-β or interferon-γ inhibited bFGF-induced changes in cell morphology, increases in cell surface αv&3 expression, and increases in &3 mRNA. These data demonstrate that both growth factors and pro-inflammatory cytokines alter the ex- pression of αvβ3 on microvascular endothelial cells and that these alterations correlate with changes in cell morphology.
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