Nettesheim P, Nakinodan T, Chadwick C J
Immunology. 1966 Nov;11(5):427-39.
Diffusion chambers (3×10 mm) constructed with 0.1 μ porosity filters, but not with 0.45 μ or greater porosity filters, were found to be consistently cell impermeable, with use of acryloid as the glueing agent. The filters permit free diffusion of 19S and 7S antibodies into `empty' chambers and . Pronase treatment of the chamber dissolves the clot and frees cells attached to the inner surfaces. This permits almost complete recovery of the chamber culture cells. Chamber cultures can be readily transferred from one host to another and kept at room temperature for at least 6 hours without any loss of activity. diffusion problems arise after 1 month of culture, most probably due to excessive growth of peritoneal cells on the outer surface of the filters; this limitation can be overcome by serial transfer of the chamber and wiping the outer surface at the time of transfer. The diffusion chamber culture method as described here fulfills all the prerequisites of an assay system with which one can perform precise cytokinetic analysis of antibody response.
用孔隙率为0.1微米的滤膜构建的扩散小室(3×10毫米),而不是孔隙率为0.45微米或更大的滤膜构建的扩散小室,被发现始终对细胞具有不可渗透性,使用丙烯酸树脂作为粘合剂。这些滤膜允许19S和7S抗体自由扩散到“空”小室中。用链霉蛋白酶处理小室可溶解凝块并释放附着在内表面的细胞。这使得小室培养细胞几乎能完全回收。小室培养物可很容易地从一个宿主转移到另一个宿主,并在室温下保存至少6小时而无任何活性损失。培养1个月后会出现扩散问题,最可能是由于滤膜外表面腹膜细胞过度生长所致;通过小室的连续转移并在转移时擦拭外表面可克服这一限制。此处所述的扩散小室培养方法满足了一种检测系统的所有先决条件,利用该系统可对抗体反应进行精确的细胞动力学分析。