The angioarchitecture of the Lewis lung carcinoma in laboratory mice (a light microscopic and scanning electron microscopic study).

Scanning electron microscopy Pub Date : 1986-01-01
T W Grunt, A Lametschwandtner, K Karrer, O Staindl
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Abstract

53 Lewis lung carcinomas implanted subcutaneously into C57BL/6-mice were examined. The animals were killed at various stages of tumor growth (TG) and prepared for histology and for scanning electron microscopy (critical-point-dried tissue; vascular corrosion casts). Prior to casting animals were rinsed using different perfusion pressures. Casting was done by manual injection of the resin, whereby different influx-rates were applied resulting in low, medium and high pressure preparations. We discern 3 phases of tumor angiogenesis (TA) occurring during 4 stages of TG among which vasodilation establishes the first reaction of the host vascular system to a growing tumor implant. During this stage 1 of TG, tumor nidation, nearby sinusoidal dilated host capillaries form globular outgrowings (phase 1 of TA). Subsequently radially arranged sprouts, which preferentially arise from venous host vessels, grow into the centre of the implant (phase 2 of TA). Stage 2 of TG, early tumor growth, is characterized by necrosis of the central tumor tissue and the development of a central avascular cavity. Thus the tumor vascular system is organized like a hollow sphere with a central cavity and a peripheral vascular "envelope" with large vessels embracing the tumor and centrifugally growing vascular sprouts, which arise from the venous part of the vascular "envelope" and invade the surrounding host tissue (phase 3 of TA). During stage 3 of TG, late tumor growth, many vessels of the basket-like vascular "envelope" obliterate. In stage 4 of TG, prefinal phase, the peripheral vascular density decreases continuously. Thus vascular sprouting and proliferation of viable tumor cells is confined to basal regions of the tumor.

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实验室小鼠Lewis肺癌的血管结构(光镜和扫描电镜研究)。
对53例C57BL/6小鼠皮下移植Lewis肺癌进行了观察。动物在肿瘤生长的各个阶段(TG)被杀死,并准备用于组织学和扫描电子显微镜(临界点干燥组织;血管腐蚀铸件)。浇铸前用不同的灌注压力冲洗动物。铸造是通过人工注射树脂来完成的,通过这种方法,施加不同的流入速率,从而产生低、中、高压制备。我们发现肿瘤血管生成(TA)发生在TG的4个阶段中的3个阶段,其中血管舒张建立了宿主血管系统对生长中的肿瘤植入物的第一反应。在TG的第1阶段,肿瘤发现,附近的正弦扩张的宿主毛细血管形成球状外生物(TA的第1阶段)。随后,放射状排列的芽,优先从静脉宿主血管产生,生长到植入物的中心(TA的第2期)。TG的第2阶段,早期肿瘤生长,特征是中心肿瘤组织坏死和中心无血管腔的发展。因此,肿瘤血管系统的组织结构像一个中空的球体,有一个中心腔和一个周围的血管“包膜”,大血管包裹着肿瘤,离心生长的血管芽从血管“包膜”的静脉部分产生,并侵入周围的宿主组织(TA的第3期)。在TG的第3期,肿瘤生长晚期,许多篮状血管“包膜”的血管消失。TG前期4期,外周血管密度持续下降。因此,血管发芽和活的肿瘤细胞的增殖被限制在肿瘤的基底区域。
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