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Background: The VEGF-Ets-1 cascades play important roles in angiogenesis by converting endothelial cells to an angiogenic phenotype. The aim of this study was to clarify whether the VEGF-Ets-1 cascades are involved in the pathogenesis of inflammatory bowel disease (IBD). Methods: Colonic specimens were taken from 42 patients with ulcerative colitis (UC), 37 with Crohn’s disease (CD), 8 with non-IBD colitis, and 21 normal controls. (1) Expression of vascular endothelial growth factor (VEGF), VEGF receptors (Flt-1, KDR), and Ets-1 proteins in colonic mucosa was immunohistochemically examined using specific antibodies. (2) Expression of Ets-1 protein or VEGF, Flt-1, KDR, and Ets-1 mRNA in colonic mucosa was measured by Western blot or RT-PCR. Results: (1) The number of VEGF containing cells was significantly increased in active UC (P < 0.05). The numbers of positive blood vessels (mean ±SE /mm2)to Flt-1, KDR, and Ets-1 antibodies were significantly increased in active UC (Flt-1: 4.0 ±0.84; KDR: 2.4 ±0.37; Ets-1: 5.5 ±0.77) compared to active CD (Flt-1: 0.6 ±0.30; KDR: 0.77 ±0.28; Ets-1: 2.0 ±0.56) (P < 0.01), non-IBD colitis (Flt-1: 1.0 ±0.45; KDR: 1.83 ±0.54; Ets-1: 3.0 ±1.0), and controls (Flt-1: 0.88 ±0.40; KDR: 0.60 ±0.22; Ets-1: 1.67 ±0.47) (P < 0.01). The numbers of positive cells to these antibodies were also increased in active UC. (2) Expression of Ets-1 protein and Flt-1, KDR, and Ets-1 mRNA was increased in active UC. Conclusions: Angiogenic factors in the VEGF-Ets-1 cascades were upregulated in UC, but they were relatively downregulated in CD. These alterations might be involved in the pathogenesis of both diseases.
Background: The VEGF-Ets-1 cascades play important roles in angiogenesis by converting endothelial cells to an angiogenic phenotype. The aim of this study was to clarify whether the VEGF-Ets-1 cascades are involved in the pathogenesis of inflammatory bowel disease (IBD (1), Expression of vascular endothelial growth factor (VEGF), and non-IBD colitis , VEGF receptors (Flt-1, KDR), and Ets-1 proteins in colonic mucosa was immunohistochemically examined using specific antibodies. (2) Expression of Ets-1 protein or VEGF, Flt-1, KDR, and Ets-1 mRNA in Colonic mucosa was measured by Western blot or RT-PCR. Results: (1) The number of VEGF containing cells was significantly increased in active UC (P <0.05). The numbers of positive blood vessels (mean ± SE / mm2) to Flt -1, KDR, and Ets-1 antibodies were significantly increased in active UC (Flt-1: 4.0 ± 0.84; Ets-1: 5.5 ± 0.77) compared to active CD (Flt-1: 0.6 ± 0.30; KDR: 0.77 ± 0.28; And IBD colitis (Flt-1: 1.0 ± 0.45; KDR: 1.83 ± 0.54; Ets-1: 3.0 ± 1.0), and controls (Flt- 1: 0.88 ± 0.40; KDR: 0.60 ± 0.22; Ets-1: 1.67 ± 0.47) (P <0.01). The numbers of positive cells to these antibodies were also increased in active UC. (2) Expression of Ets-1 protein and Flt-1, KDR, and Ets-1 mRNA was increased in active UC. Conclusions: Angiogenic factors in the VEGF-Ets-1 cascades were upregulated in UC, but they were relatively downregulated in CD. These alterations might be involved in the pathogenesis of both diseases.