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人类结直肠癌基质中的微血管变化:超微结构组织化学研究

Microvascular changes in the stroma of human colorectal carcinomas: ultrastructural histochemical study.

作者信息

Ohtani H, Sasano N

机构信息

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

出版信息

Jpn J Cancer Res. 1989 Apr;80(4):360-5. doi: 10.1111/j.1349-7006.1989.tb02320.x.

Abstract

Ultrastructural histochemical studies were performed using Ulex europaeus agglutinin-I lectin (UEA-I) and anti-endothelial monoclonal antibody BMA 120 in order to morphologically characterize the microvasculature of human colorectal carcinomas. In the normal mucosa, UEA-I and BMA 120 were bound to luminal plasma membrane of endothelial cells, usually continuously. Capillaries in the stroma of invasive adenocarcinomas showed remarkable structural changes such as swelling of endothelial cells with well-developed cell organelles and narrowing of the lumen. Reaction products for UEA-I and BMA 120 were both observed along the luminal plasma membrane of endothelial cells, usually discontinuously, partially retaining the features of normal capillaries. Furthermore, we have confirmed an occurrence of solid capillary buds composed of a strand of large endothelial cells with a trace of lumen. They showed almost no reactivity to UEA-I and BMA 120. Conventional electron microscopy revealed that they were present frequently in invasive carcinomas, but infrequently in intramucosal carcinomas and inflammatory lesions. Our results suggest that the stroma of invasive colorectal carcinomas abounds in immature capillaries and their precursors, which may indicate active tumor-induced angiogenesis.

摘要

为了从形态学上表征人大肠癌的微血管系统,我们使用荆豆凝集素-I(UEA-I)和抗内皮细胞单克隆抗体BMA 120进行了超微结构组织化学研究。在正常黏膜中,UEA-I和BMA 120通常连续地结合在内皮细胞的管腔质膜上。浸润性腺癌基质中的毛细血管显示出显著的结构变化,如内皮细胞肿胀且细胞器发达,管腔变窄。UEA-I和BMA 120的反应产物均在内皮细胞的管腔质膜上观察到,通常不连续,部分保留了正常毛细血管的特征。此外,我们证实了由一串带有微量管腔的大内皮细胞组成的实性毛细血管芽的存在。它们对UEA-I和BMA 120几乎无反应。传统电子显微镜显示,它们在浸润性癌中频繁出现,但在黏膜内癌和炎性病变中很少见。我们的结果表明,浸润性大肠癌的基质中富含未成熟的毛细血管及其前体,这可能表明存在活跃的肿瘤诱导血管生成。

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Angiogenesis in vitro.体外血管生成
Nature. 1980 Dec 11;288(5791):551-6. doi: 10.1038/288551a0.

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