More L, Sim R, Hudson M, Dhillon A P, Pounder R, Wakefield A J
University Department of Histopathology, Royal Free Hospital School of Medicine, London.
J Clin Pathol. 1993 Aug;46(8):703-8. doi: 10.1136/jcp.46.8.703.
To investigate the localisation of tissue factor expression in normal and inflamed intestine.
Serial cryostat sections of tissue taken from patients with Crohn's disease (n = 8), ulcerative colitis (n = 5), and from controls (n = 5) were stained with haematoxylin and eosin and immunostained for tissue factor, collagen type IV, fibrinogen and platelet glycoprotein IIIa.
In control tissues tissue factor was present as a continuous layer along the epithelial basal lamina: sections from controls did not immunostain for fibrinogen or platelets. In non-ulcerated inflamed mucosa, tissue factor staining intensified in cases of Crohn's disease and was associated with fibrin deposition. Staining for tissue factor was either patchy or absent in cases of ulcerative colitis and there was no fibrin deposition. This change accompanied the early destruction of the epithelial basal lamina in ulcerative colitis that was not seen in Crohn's disease. In both diseases tissue factor expression in severely inflamed and ulcerated mucosa was present on lamina propria macrophages and vascular endothelium and was associated with fibrin or platelet thrombi. In three of eight cases of Crohn's disease tissue factor expression and thrombi were evident in areas of submucosal vasculitis. These were not seen in adjacent normal vessels.
These observations are consistent with a tissue factor haemostatic barrier in the intestine: this barrier seems to be incomplete or defective in ulcerative colitis. Tissue factor expression by macrophages and endothelial cells may be important, particularly in the microvascular thrombosis and induration which are characteristic of Crohn's disease.
研究组织因子在正常和发炎肠道中的表达定位。
对取自克罗恩病患者(n = 8)、溃疡性结肠炎患者(n = 5)及对照组(n = 5)的组织连续进行冰冻切片,用苏木精和伊红染色,并对组织因子、IV型胶原、纤维蛋白原和血小板糖蛋白IIIa进行免疫染色。
在对照组织中,组织因子沿上皮基底层呈连续层存在:对照组切片未对纤维蛋白原或血小板进行免疫染色。在非溃疡性发炎黏膜中,克罗恩病患者的组织因子染色增强,并与纤维蛋白沉积有关。溃疡性结肠炎患者的组织因子染色呈斑片状或无染色,且无纤维蛋白沉积。这种变化伴随着溃疡性结肠炎中上皮基底层的早期破坏,而克罗恩病中未见此现象。在两种疾病中,严重发炎和溃疡黏膜中的组织因子表达存在于固有层巨噬细胞和血管内皮细胞上,并与纤维蛋白或血小板血栓有关。在8例克罗恩病患者中的3例,黏膜下血管炎区域可见组织因子表达和血栓形成。相邻正常血管中未见此现象。
这些观察结果与肠道中的组织因子止血屏障一致:在溃疡性结肠炎中,这种屏障似乎不完整或有缺陷。巨噬细胞和内皮细胞的组织因子表达可能很重要,尤其是在克罗恩病特有的微血管血栓形成和硬结方面。