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首页> 外文期刊>British Journal of Cancer >Plasminogen activator in cultured Lewis lung carcinoma cells measured by chromogenic substrate assay
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Plasminogen activator in cultured Lewis lung carcinoma cells measured by chromogenic substrate assay

机译:显色底物测定法测量培养的Lewis肺癌细胞中的纤溶酶原激活剂

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A chromogenic substrate assay for the plasminogen activator (PA) activity of Lewis lung carcinoma cells has been developed. The cells were incubated with plasminogen, the activation of which to plasmin was measured by the amidolysis of the chromogenic substrate S-2251. This was routinely performed as a 4h serum-free assay, but a variation lasting 24 h, in medium supplemented with plasminogen-free inhibitor-reduced serum, produced similar results. The assay also detected PA released into the medium. PA activity was proportional to cell density, and the assay was non-toxic to the cells. Assays were performed on cultures derived from primary and metastatic tumours. Host cells were effectively eliminated from such cultures but, because of an initial phase of tumour-cell death, PA assays were not carried out until cultures became established. No consistent difference was detected between PA levels in primary and metastatic cultures. However, these cultures were shown to be atypical of the parent tumour, they grew slowly when reinjected at the primary site, and their metastatic potential was impaired.
机译:已经开发了用于Lewis肺癌细胞纤溶酶原激活物(PA)活性的生色底物测定法。将细胞与纤溶酶原一起温育,通过发色底物S-2251的酰胺化来测量其对纤溶酶的活化。这通常按4小时无血清测定法进行,但在补充有无纤溶酶原抑制剂降低血清的培养基中,持续24小时的变化也产生了相似的结果。该测定法还检测到释放到培养基中的PA。 PA活性与细胞密度成正比,并且该测定对细胞无毒。对源自原发性和转移性肿瘤的培养物进行测定。宿主细胞被有效地从这种培养物中消除,但是由于肿瘤细胞死亡的初始阶段,直到培养物建立后才进行PA测定。在原代和转移培养中,PA水平之间未发现一致的差异。然而,这些培养物被证明是非典型的亲本肿瘤,当在原发部位再次注射时,它们生长缓慢,并且转移潜能受损。

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