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一种骨源性肿瘤细胞趋化因子的部分特性

Partial characterization of a bone-derived chemotactic factor for tumor cells.

作者信息

Orr F W, Varani J, Gondek M D, Ward P A, Mundy G R

出版信息

Am J Pathol. 1980 Apr;99(1):43-52.

Abstract

Medium that has been bathing organ cultures of resorbing bone contains a factor that is chemotactic for cultured Walker carcinosarcoma cells, as assayed by the Boyden chamber technique. There is a positive correlation between the chemotactic activity released by the resorbing bones and the extent of resorption as measured by release of previously incorporated 45Ca from the bones. Generation of the chemotactic factor occurs independent of the humoral mediator of bone resorption. The tumor cell chemotactic factor has a steep dose-response curve, with a fall from maximal to minimal activity extending over a four-fold dilution. The chemotactic activity is stable to heating and has an estimated molecular weight of 6000 daltons, as determined by gel filtration chromatography and retention of activity following dialysis. The chemotactic activity has been distinguished from the tumor cell chemotactic factor derived from the fifth component of complement because the former is not inactivated by antiserum to C5 and because it is chemotactic for EL-4 lymphoma cells, whereas the latter is not chemotactically active for these cells.

摘要

用博伊登小室技术检测发现,用于浸泡正在吸收的骨器官培养物的培养基中含有一种对培养的沃克癌肉瘤细胞具有趋化作用的因子。正在吸收的骨释放的趋化活性与骨吸收程度之间存在正相关,骨吸收程度通过测量先前掺入骨中的45Ca的释放量来确定。趋化因子的产生与骨吸收的体液介质无关。肿瘤细胞趋化因子具有陡峭的剂量反应曲线,从最大活性降至最小活性的范围为四倍稀释。趋化活性对加热稳定,通过凝胶过滤色谱法和透析后活性保留测定,其估计分子量为6000道尔顿。这种趋化活性已与源自补体第五成分的肿瘤细胞趋化因子区分开来,因为前者不会被抗C5血清灭活,并且对EL-4淋巴瘤细胞具有趋化作用,而后者对这些细胞没有趋化活性。

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