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两种主要类型胃癌的微血管差异:血管性血友病因子的传统、超微结构及超微结构免疫定位研究

Differing microvasculature in the two major types of gastric carcinoma: a conventional, ultrastructural and ultrastructural immunolocalization study of von Willebrand factor.

作者信息

Ohtani H, Nagura H

机构信息

Department of Pathology, Tohoku University School of Medicine, Sendai, Japan.

出版信息

Virchows Arch A Pathol Anat Histopathol. 1990;417(1):29-35. doi: 10.1007/BF01600106.

Abstract

The microvasculature of the stroma of human gastric carcinoma was studied by immuno-electron microscopy for factor VIII/von Willebrand factor (vWF) and conventional electron microscopy. In differentiated type (intestinal) gastric carcinoma (9 cases), capillaries were distributed more densely around carcinoma cell nests. vWF was localized in endothelial cells and neighbouring stroma. Ultrastructurally, capillary endothelial cells showed considerable hypertrophic changes with well-developed rough endoplasmic reticulum (rER). vWF was localized in well-developed rER, granules, Weibel-Palade bodies (WPB), in the vascular lumen as clusters, and diffusely deposited in the subendothelium. This indicates that endothelial cells in this group are transformed into a state of active protein production. In undifferentiated type (diffuse) gastric carcinoma (12 cases), capillaries were uniformly distributed and endothelial hypertrophic changes were less remarkable. vWF was localized in WPB, scanty rER and subendothelial matrix. Solid capillary buds were observed in both types; they were composed of a solid strand of endothelial cells without a visible lumen. Our results reveal that the microvasculature in tumour stroma differs significantly according to its histological type.

摘要

通过免疫电子显微镜检测因子VIII/血管性血友病因子(vWF)以及传统电子显微镜,对人胃癌基质的微血管系统进行了研究。在分化型(肠型)胃癌(9例)中,毛细血管在癌细胞巢周围分布更为密集。vWF定位于内皮细胞和邻近的基质中。超微结构上,毛细血管内皮细胞显示出明显的肥大变化,粗面内质网(rER)发达。vWF定位于发达的rER、颗粒、魏尔-帕拉德小体(WPB)中,在血管腔内呈簇状分布,并弥散沉积于内皮下。这表明该组内皮细胞转变为活跃的蛋白质产生状态。在未分化型(弥漫型)胃癌(12例)中,毛细血管分布均匀,内皮肥大变化不太明显。vWF定位于WPB、少量rER和内皮下基质中。在两种类型中均观察到实性毛细血管芽;它们由一束无可见管腔的实性内皮细胞组成。我们的结果显示,肿瘤基质中的微血管系统根据其组织学类型有显著差异。

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