Fish R. G., Pritchard J. A. V., Deeley T. J.
Br J Cancer. 1974 Sep;30(3):222-30.
The interaction of the highly purified basic protein "antigen", calf thymus histone F2A1 fraction, with peripheral lymphocytes isolated from patients with cancer and from normal subjects has been studied. Analysis, by SDS polyacrylamide gel electrophoresis of the basic protein remaining in the supernatant fluid after interaction with low concentrations of lymphocytes from patients showed the presence of a component(s) of molecular weight smaller than the original histone F2A1 fraction. Similar experiments using lymphocytes derived from normal subjects indicated that this component(s) is absent, or at least is present in only small amounts. This difference could be partially abolished by using high concentrations of cell preparations. It is suggested that the observed difference is due at least in part, to differences in protease activity between the two preparations. The possible significance of these findings in relation to the macrophage electrophoretic mobility test for cancer is discussed.
对高纯度碱性蛋白“抗原”,即小牛胸腺组蛋白F2A1组分,与从癌症患者和正常受试者分离出的外周淋巴细胞之间的相互作用进行了研究。通过SDS聚丙烯酰胺凝胶电泳分析与低浓度癌症患者淋巴细胞相互作用后上清液中剩余的碱性蛋白,结果显示存在分子量小于原始组蛋白F2A1组分的一种或多种成分。使用来自正常受试者的淋巴细胞进行的类似实验表明,这种成分不存在,或至少仅少量存在。通过使用高浓度细胞制剂,这种差异可部分消除。提示观察到的差异至少部分归因于两种制剂之间蛋白酶活性的差异。讨论了这些发现与癌症巨噬细胞电泳迁移率试验相关的可能意义。