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利用血管内皮细胞单层进行转移性肿瘤细胞附着和侵袭试验。

Metastatic tumor cell attachment and invasion assay utilizing vascular endothelial cell monolayers.

作者信息

Nicolson G L

出版信息

J Histochem Cytochem. 1982 Mar;30(3):214-20. doi: 10.1177/30.3.7061823.

Abstract

Two of the more important steps in blood-borne tumor metastasis are attachment of the circulating malignant cells to the vascular endothelium and subsequent extravasation or invasion out of the blood vessel. A model for this process has been developed using cultured monolayers of vascular endothelial cells that synthesize a basal lamina or extracellular matrix (Kramer and Nicolson, Proc Natl Acad Sci USA 76:504, 1979). We have used this model to study metastatic tumor cell-endothelial cell interactions such as attachment to endothelial cells and their subsequent retraction and exposure of endothelial basal lamina as well as the interactions of metastatic tumor cells with the basal lamina leading to invasion and solubilization of this extracellular matrix. Morphological, immunological, and enzymological analysis of these steps in the metastatic process can be obtained using the vascular endothelial cell monolayer model for attachment and invasion.

摘要

血源性肿瘤转移过程中两个较为重要的步骤是循环中的恶性细胞附着于血管内皮,以及随后穿出血管或侵入血管外。利用合成基膜或细胞外基质的血管内皮细胞培养单层建立了该过程的模型(Kramer和Nicolson,《美国国家科学院院刊》76:504,1979年)。我们已使用该模型研究转移性肿瘤细胞与内皮细胞的相互作用,如附着于内皮细胞及其随后的收缩以及内皮基膜的暴露,以及转移性肿瘤细胞与基膜的相互作用导致这种细胞外基质的侵袭和溶解。使用血管内皮细胞单层模型进行附着和侵袭,可以对转移过程中这些步骤进行形态学、免疫学和酶学分析。

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