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V2癌细胞侵袭的兔肠系膜中肿瘤周围蛋白聚糖改变的形态学

Morphology of peritumoral proteoglycan alterations in the rabbit mesentery invaded by V2 carcinoma cells.

作者信息

Müller-Glauser W, Haemmerli G, In-Albon A, Sträuli P

出版信息

Int J Cancer. 1984 Oct 15;34(4):545-53. doi: 10.1002/ijc.2910340418.

Abstract

After intraperitoneal implantation into Swiss Silver rabbits, V2 rabbit carcinoma cells invade the mesentery where they form nodules of different size and texture: compact (less than 120 microns in diameter), loose (120-250 microns) and mixed (above 200 microns). Together with tumor development, certain changes take place in the loose connective tissue of the mesentery. Application of TEM, together with use of safranin O, has shown that, in areas free of tumor growth, collagen bundles become thick and heavy and proteoglycan density is increased. Concurrently, the number of fibrocytes, now transformed to fibroblasts, increases. Small, compact nodules are surrounded by a concentrically arranged extracellular matrix. Its overall density is similar to that of nodule-free areas. In the immediate vicinity of large, loose nodules, all constituents of the extracellular matrix disappear. Adjacent connective tissue is partly destroyed but still contains collagen fibers and proteoglycans. These findings suggest the following: The presence of V2 carcinoma cells induces marked alterations in the structured and non-structured components of the extracellular matrix. These changes are, at the same time, progressive and regressive and the occurrence of one or the other depends on local tumor progression. Progressive alterations may result from an increased activity of fibroblasts. Since degradative effects, on the other hand, are only seen in the immediate vicinity of larger tumor aggregates, it is assumed that a minimal number of tumor cells is essential for destruction of extracellular matrix.

摘要

将V2兔癌细胞腹腔内植入瑞士银兔后,癌细胞侵入肠系膜,在那里形成大小和质地各异的结节:致密结节(直径小于120微米)、疏松结节(120 - 250微米)和混合结节(直径大于200微米)。随着肿瘤的发展,肠系膜的疏松结缔组织会发生某些变化。透射电子显微镜(TEM)与番红O染色联合应用显示,在无肿瘤生长的区域,胶原束变粗且增多,蛋白聚糖密度增加。同时,已转化为成纤维细胞的纤维细胞数量增多。小的致密结节被同心排列的细胞外基质包围。其总体密度与无结节区域相似。在大的疏松结节附近,细胞外基质的所有成分均消失。相邻的结缔组织部分被破坏,但仍含有胶原纤维和蛋白聚糖。这些发现提示:V2癌细胞的存在会引起细胞外基质的结构化和非结构化成分发生显著改变。这些变化同时具有进行性和退行性,其发生何种变化取决于局部肿瘤的进展情况。进行性改变可能是由于成纤维细胞活性增加所致。另一方面,降解作用仅在较大肿瘤聚集体附近可见,因此推测最少数量的肿瘤细胞对于细胞外基质的破坏至关重要。

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