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CD44在胶质瘤细胞与细胞外基质成分之间的黏附相互作用中发挥作用。

CD44 plays a role in adhesive interactions between glioma cells and extracellular matrix components.

作者信息

Radotra B, McCormick D, Crockard A

机构信息

Neuro-Oncology Laboratory, Queen's University of Belfast, UK.

出版信息

Neuropathol Appl Neurobiol. 1994 Aug;20(4):399-405. doi: 10.1111/j.1365-2990.1994.tb00986.x.

Abstract

Glioma invasion is a complex process involving interactions of tumour cells with host cells and extracellular matrix (ECM). The initial event in the process is recognition and attachment of glioma cells to specific ECM molecules prior to migration into proteolytically modified matrix. In comparison with other tissues, brain ECM is a relatively amorphous matrix which contains glycosaminoglycans including hyaluronan (HA). Recently CD44 which is a transmembrane adhesion molecule found on a wide variety of cells, has been suggested as the principal cell surface receptor for HA. In the present in vitro investigation we have analysed the role of CD44 in adhesive interactions between human gliomas and ECM. Our experimental procedures included immunocytochemistry, immunoblotting, in vitro adhesion assay and flow cytometry. CD44 was expressed on the surface of all gliomas analysed (9) and the level of expression showed no correlation with tumour grade. Eighty, 95 and 120 kDa isoforms were demonstrated by immunoblotting. In an adhesion blocking assay it was found that ligation of CD44 with specific antibody resulted in reduced adhesion to hyaluronan, chondroitin sulphate, fibronectin, laminin, collagen IV and Matrigel. We conclude that CD44 is involved in adhesion of glioma cells to a wide range of ECM components.

摘要

胶质瘤侵袭是一个复杂的过程,涉及肿瘤细胞与宿主细胞及细胞外基质(ECM)的相互作用。该过程的初始事件是胶质瘤细胞在迁移到经蛋白水解修饰的基质之前,识别并附着于特定的ECM分子。与其他组织相比,脑ECM是一种相对无定形的基质,含有包括透明质酸(HA)在内的糖胺聚糖。最近,CD44作为一种在多种细胞上发现的跨膜黏附分子,被认为是HA的主要细胞表面受体。在本体外研究中,我们分析了CD44在人胶质瘤与ECM黏附相互作用中的作用。我们的实验程序包括免疫细胞化学、免疫印迹、体外黏附试验和流式细胞术。在所分析的所有胶质瘤(9例)表面均表达CD44,且表达水平与肿瘤分级无关。免疫印迹显示有80、95和120 kDa的异构体。在黏附阻断试验中发现,用特异性抗体连接CD44会导致对透明质酸、硫酸软骨素、纤连蛋白、层粘连蛋白、IV型胶原和基质胶的黏附减少。我们得出结论,CD44参与胶质瘤细胞与多种ECM成分的黏附。

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