Calderon J, Williams R T, Unanue E R
Proc Natl Acad Sci U S A. 1974 Nov;71(11):4273-7. doi: 10.1073/pnas.71.11.4273.
Culture fluids from mouse peritoneal exudate cells inhibited [(3)H]thymidine incorporation by, and proliferation of, EL-4 leukemia cells, 3T3 cells, and mitogen-stimulated spleen lymphocytes. Inhibited EL-4 leukemia cells recovered their normal proliferative capacity when washed and incubated in normal medium. The inhibitory activity resided in a low-molecular-weight substance that could be absorbed by incubation with the tumor cells. This substance was dialyzable and resistant to tryptic digestion and phosphodiesterase treatment. The mononuclear phagocytes in the peritoneal exudate seemed to be the source of the inhibitor. The inhibitory material was found in the same amounts in exudates of normal mice or mice injected with peptone or infected with Listeria monocytogenes; spleen cells adherent to plastic released the inhibitor but in lesser amount. We suggest that this inhibitor may contribute to the deleterious effects found when various cells, including neoplastic ones, are cultured in the presence of macrophages.
来自小鼠腹腔渗出细胞的培养液抑制了EL-4白血病细胞、3T3细胞以及丝裂原刺激的脾淋巴细胞的[³H]胸腺嘧啶核苷掺入及其增殖。被抑制的EL-4白血病细胞经洗涤并在正常培养基中培养后恢复了其正常增殖能力。抑制活性存在于一种低分子量物质中,该物质可通过与肿瘤细胞孵育而被吸收。这种物质可透析,且对胰蛋白酶消化和磷酸二酯酶处理具有抗性。腹腔渗出液中的单核吞噬细胞似乎是抑制剂的来源。在正常小鼠、注射蛋白胨或感染单核细胞增生李斯特菌的小鼠的渗出液中发现的抑制物质含量相同;附着于塑料的脾细胞释放抑制剂,但量较少。我们认为,当包括肿瘤细胞在内的各种细胞在巨噬细胞存在的情况下培养时,这种抑制剂可能会导致有害影响。