Griga Thomas, Tromm Andreas, Schmiegel Wolff, Pfisterer Okka, Müller Klaus-M, Brasch Frank
Department of Gastroenterology, University Hospital Bergmannsheil, Ruhr-University, Bochum, Germany.
Eur J Gastroenterol Hepatol. 2004 Apr;16(4):397-402. doi: 10.1097/00042737-200404000-00005.
Collagenous colitis is a chronic inflammatory bowel disease with a band-like subepithelial deposition of immature extracellular matrix. Because the extracellular matrix deposition is potentially reversible, an imbalance between fibrogenesis and fibrolysis with reduced matrix degradation has been suspected. Vascular endothelial growth factor plays a central role in extracellular matrix degradation. Therefore, we investigated the expression of vascular endothelial growth factor in the colonic mucosa of patients with collagenous colitis before and after long-term treatment with oral budesonide.
A quantitative immunohistochemical method was used to measure the amount of immunoreactive vascular endothelial growth factor, tenascin and leucocyte common antigen within the epithelium and the lamina propria of colonic biopsies by area morphometry.
Strong immunostaining for vascular endothelial growth factor within the epithelium and the lamina propria, and for tenascin, was seen in patients with collagenous colitis compared with normal controls. The enhanced immunostaining for vascular endothelial growth factor within the lamina propria was accompanied by the accumulation of leucocytes, detected by staining for leucocyte common antigen. After long-term treatment with oral budesonide, the amount of immunostaining for leucocyte-derived vascular endothelial growth factor within the lamina propria decreased significantly to normal levels. In contrast, staining for vascular endothelial growth factor within the epithelium remained significantly increased.
Our data suggest an important role of vascular endothelial growth factor in counteracting the local imbalance of fibrogenesis and fibrolysis, leading to an accumulation of immature subepithelial matrix in collagenous colitis.
胶原性结肠炎是一种慢性炎症性肠病,其特征为未成熟细胞外基质在黏膜下呈带状沉积。由于细胞外基质沉积可能是可逆的,因此人们怀疑纤维生成与纤维溶解之间存在失衡,导致基质降解减少。血管内皮生长因子在细胞外基质降解中起核心作用。因此,我们研究了口服布地奈德长期治疗前后胶原性结肠炎患者结肠黏膜中血管内皮生长因子的表达情况。
采用定量免疫组织化学方法,通过面积形态计量法测量结肠活检组织上皮和固有层中免疫反应性血管内皮生长因子、腱生蛋白和白细胞共同抗原的含量。
与正常对照组相比,胶原性结肠炎患者的上皮和固有层中血管内皮生长因子以及腱生蛋白呈强免疫染色。固有层中血管内皮生长因子免疫染色增强的同时,通过白细胞共同抗原染色检测到白细胞聚集。口服布地奈德长期治疗后,固有层中白细胞衍生的血管内皮生长因子免疫染色量显著降低至正常水平。相比之下,上皮中血管内皮生长因子的染色仍显著增加。
我们的数据表明血管内皮生长因子在对抗胶原性结肠炎中纤维生成和纤维溶解的局部失衡方面发挥重要作用,这种失衡导致未成熟的上皮下基质积累。