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Development of Arterial Blood Supply in Experimental Liver Metastases

机译:实验性肝转移中动脉血供的发展

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摘要

In this study, we present a mechanism for the development of arterial blood supply in experimental liver metastases. To analyze the arterialization process of experimental liver metastases, we elucidated a few key questions regarding the blood supply of hepatic lobules in mice. The microvasculature of the mouse liver is characterized by numerous arterioportal anastomoses and arterial terminations at the base of the lobules. These terminations supply one hepatic microcirculatory subunit per lobule, which we call an arterial hepatic microcirculatory subunit (aHMS). The process of arterialization can be divided into the following steps: 1) distortion of the aHMS by metastasis; 2) initial fusion of the sinusoids of the aHMS at the tumor parenchyma interface; 3) fusion of the sinusoids located at the base of the aHMSs, which leads to the disruption of the vascular sphincter (burst pipe); 4) incorporation of the dilated artery and the fused sinusoids into the tumor; and 5) further development of the tumor vasculature (arterial tree) by proliferation, remodeling, and continuous incorporation of fused sinusoids at the tumor–parenchyma interface. This process leads to the inevitable arterialization of liver metastases above the 2000- to 2500-μm size, regardless of the origin and growth pattern of the tumor.
机译:在这项研究中,我们提出了在实验性肝转移中发展动脉血供的机制。为了分析实验性肝转移的动脉化过程,我们阐明了有关小鼠肝小叶供血的几个关键问题。小鼠肝脏的微脉管系统的特征是众多的小门静脉吻合和小叶基部的动脉末端。这些末端每个小叶提供一个肝微循环亚基,我们称其为动脉肝微循环亚基(aHMS)。动脉化过程可分为以下步骤:1)转移引起的aHMS畸变; 2)在肿瘤实质界面处aHMS的正弦曲线的初始融合; 3)位于aHMS底部的正弦融合,导致血管括约肌(爆裂管)破裂; 4)将扩张的动脉和融合的正弦波合并到肿瘤中; 5)通过扩散,重塑以及在肿瘤与实质之间的界面不断融合融合的正弦波,进一步发展肿瘤脉管系统(动脉树)。无论肿瘤的起源和生长方式如何,此过程都会导致2000-2500μm以上的肝转移不可避免地发生动脉化。

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