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实验性脑转移中肾小球样体形成的新概念。

A novel concept of glomeruloid body formation in experimental cerebral metastases.

作者信息

Döme Balázs, Tímár József, Paku Sándor

机构信息

First Institute of Pathology and Experimental Cancer Research, Semmelweis University, Budapest, Hungary.

出版信息

J Neuropathol Exp Neurol. 2003 Jun;62(6):655-61. doi: 10.1093/jnen/62.6.655.

Abstract

Glomeruloid bodies (GBs), tumor-associated vascular structures with a superficial resemblance to renal glomeruli, are important histopathological features of glioblastoma multiforme, but have also been described in other types of tumors and in cerebral metastases. The purpose of this study was to elucidate the pathogenesis of these lesions in an appropriate murine model of experimental brain metastases. To do so, we injected cells from 5 different tumor lines into the internal carotid artery of mice and investigated the development, composition, and fate of GBs growing within tumor nodules. Immunohistochemical analyses and 3-dimensional reconstruction of the cerebral vasculature showed clearly that the proliferating and migrating tumor cells pull the capillaries (and the adjacent capillary branching points) into the tumor cell nest. Initially, this process lead to the appearance of simple coiled vascular structures, which later developed into chaotic and tortuous vascular aggregates with multiple narrowed afferent and efferent microvessels. Despite the absence of sprouting angiogenesis, the very low level of endothelial cell proliferation index and the ruptures of the stretched and narrowed capillary segments observed frequently between the metastatic tumor nodules, necrosis was scarce in these lesions, implying that the blood supply from the multiple afferent microvessels and from the preexistent vascular bed sufficed to provide the tumor cells with oxygen and nutrients.

摘要

肾小球样小体(GBs)是一种与肾小体表面相似的肿瘤相关血管结构,是多形性胶质母细胞瘤的重要组织病理学特征,但在其他类型的肿瘤和脑转移瘤中也有描述。本研究的目的是在合适的实验性脑转移小鼠模型中阐明这些病变的发病机制。为此,我们将来自5种不同肿瘤系的细胞注入小鼠颈内动脉,并研究肿瘤结节内生长的GBs的发育、组成和转归。免疫组织化学分析和脑血管的三维重建清楚地表明,增殖和迁移的肿瘤细胞将毛细血管(以及相邻的毛细血管分支点)拉入肿瘤细胞巢。最初,这一过程导致简单盘绕的血管结构出现,随后发展为具有多个狭窄的传入和传出微血管的混乱且迂曲的血管聚集体。尽管没有发芽性血管生成,内皮细胞增殖指数极低,且在转移性肿瘤结节之间经常观察到拉伸和狭窄的毛细血管段破裂,但这些病变中坏死很少,这意味着来自多个传入微血管和先前存在的血管床的血液供应足以向肿瘤细胞提供氧气和营养。

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