Akeson R, Herschman H R
Proc Natl Acad Sci U S A. 1974 Jan;71(1):187-91. doi: 10.1073/pnas.71.1.187.
Antisera were produced in rabbits to morphologically differentiated cells from the C1300 murine neuroblastoma (i.e., cells in which process formation was induced by maintenance on serum-free medium for 5 days). These antisera reacted more strongly in the complement fixation reaction with such "differentiated" cells than with "undifferentiated" (nonprocess-bearing) neuroblastoma cells. Adsorption of the antisera with undifferentiated cells removed the reactivity to cells without processes, while the reactivity with serum-free cells which possess processes was retained. Indirect immunofluorescence studies confirmed the results obtained by complement fixation and demonstrated that antibodies to the surface antigens of process-bearing cells could be adsorbed by particulate preparations from brain but not liver, spleen, or kidney. This is the first description of neural-associated cell-surface changes that correlate with the morphological differentiation in culture of neuroblastoma cells.
用来自C1300小鼠神经母细胞瘤形态学上已分化的细胞(即在无血清培养基上维持5天诱导出突起形成的细胞)免疫家兔制备抗血清。这些抗血清在补体结合反应中与这类“已分化”细胞的反应比与“未分化”(无突起)神经母细胞瘤细胞的反应更强。用未分化细胞吸附抗血清可消除对无突起细胞的反应性,而对有突起的无血清培养细胞的反应性则得以保留。间接免疫荧光研究证实了补体结合反应的结果,并表明针对有突起细胞表面抗原的抗体可被脑的颗粒制剂吸附,但不能被肝、脾或肾的颗粒制剂吸附。这是首次描述与神经母细胞瘤细胞培养中的形态学分化相关的神经相关细胞表面变化。