Krishnan V L, Humphrey J H
Br J Exp Pathol. 1986 Dec;67(6):809-19.
Resident peritoneal macrophages, spleen macrophages and Kupffer cells isolated from normal CBA mice were treated with supernatants from spleen cells of normal or immunized mice, and cultured in the presence of heat-killed Listeria monocytogenes. The capacity of the macrophages, infected in vitro, to control the growth of Listeria was tested. In macrophages treated with supernatant from normal spleen cells, the organisms multiplied extensively during 24 h but in those treated with supernatant from immune spleen cells, growth was greatly inhibited. Macrophages isolated from mice irradiated with 8-9.5 Gy and treated with immune spleen cell supernatant, were as efficient or even more than those from unirradiated mice. The use of multispot slides proved to be a convenient and economical means of culturing and examining cells.
从正常CBA小鼠分离出的腹腔巨噬细胞、脾巨噬细胞和库普弗细胞,用正常或免疫小鼠脾细胞的上清液处理,并在热灭活的单核细胞增生李斯特菌存在的情况下进行培养。测试了体外感染的巨噬细胞控制李斯特菌生长的能力。在用正常脾细胞上清液处理的巨噬细胞中,细菌在24小时内大量繁殖,但在用免疫脾细胞上清液处理的巨噬细胞中,生长受到极大抑制。从接受8-9.5 Gy照射并用免疫脾细胞上清液处理的小鼠中分离出的巨噬细胞,与未照射小鼠的巨噬细胞一样有效,甚至更有效。事实证明,使用多斑点载玻片是培养和检查细胞的一种方便且经济的方法。