Callahan G N, Allison J P, Pellegrino M A, Reisfeld R A
J Immunol. 1979 Jan;122(1):70-4.
Serologic and immunochemical techniques were used to characterize plasma membrane antigens of the murine lymphoma 6C3HED. Syngeneic C3H/HeJ anti-6C3HED antisera were prepared and were shown by cytotoxicity, absorption, and immunoprecipitation tests to be specifically reactive with the lymphoma cells. Alloantisera to H-2.23 were found to be unreactive with intact lymphoma cells by cytotoxicity and absorption assays. However, H-2.23 antigens were detectable in tumor cell lysates by inhibition of cytotoxicity and immunoprecipitation. SDS-PAGE electropherograms of immunoprecipitates of radiolabeled tumor cell extracts obtained with anti-6C3HED and anti-H2.23 antisera were essentially identical; proteins with Mr of approximately 70,000, 45,000, and 12,000 were apparent in both. An immuno-adsorbent of insolubilized anti-6C3HED removed H-2.23 antigens detectable in lymphoma extracts, but had no effect on H-2.23 antigens in normal splenocyte extracts. These data indicate that H-2.23 and TAA are physically associated on 6C3HED cells.
采用血清学和免疫化学技术对鼠淋巴瘤6C3HED的质膜抗原进行表征。制备了同基因C3H/HeJ抗6C3HED抗血清,并通过细胞毒性、吸收和免疫沉淀试验表明其与淋巴瘤细胞具有特异性反应。通过细胞毒性和吸收试验发现,针对H-2.23的同种抗血清与完整的淋巴瘤细胞无反应。然而,通过细胞毒性抑制和免疫沉淀可在肿瘤细胞裂解物中检测到H-2.23抗原。用抗6C3HED和抗H2.23抗血清获得的放射性标记肿瘤细胞提取物免疫沉淀的SDS-PAGE电泳图谱基本相同;两者中均可见分子量约为70,000、45,000和12,000的蛋白质。固定化抗6C3HED的免疫吸附剂去除了淋巴瘤提取物中可检测到的H-2.23抗原,但对正常脾细胞提取物中的H-2.23抗原无影响。这些数据表明,H-2.23和肿瘤相关抗原(TAA)在6C3HED细胞上存在物理关联。