Garzelli C, Campa M, Forlani A, Colizzi V, Falcone G
Int Arch Allergy Appl Immunol. 1982;69(2):143-7. doi: 10.1159/000233162.
The effect of bacterial lipopolysaccharide (LPS) on the development of plaque-forming cells (PFC) against bromelain-treated syngeneic mouse red blood cells (Br-MRBC) was studied in peritoneal cell (PC) cultures. It was found that LPS enhances the development of PFC to Br-MRBC and increases DNA synthesis in PC cultures. The LPS-induced enhancement of PFC to Br-MRBC, however, does not appear to require cell proliferation, since it also occurred in PC cultures pretreated with mitomycin C. In addition, the LPS-induced B lymphocytes blastogenesis is under the control of macrophages, while cell differentiation of precursor B lymphocytes into cells actively producing antibodies against Br-MRBC is regulated by suppressor T lymphocytes.
在腹膜细胞(PC)培养物中研究了细菌脂多糖(LPS)对针对菠萝蛋白酶处理的同基因小鼠红细胞(Br-MRBC)的斑块形成细胞(PFC)发育的影响。发现LPS增强了PFC对Br-MRBC的发育,并增加了PC培养物中的DNA合成。然而,LPS诱导的PFC对Br-MRBC的增强似乎不需要细胞增殖,因为它也发生在用丝裂霉素C预处理的PC培养物中。此外,LPS诱导的B淋巴细胞增殖受巨噬细胞控制,而前体B淋巴细胞向积极产生抗Br-MRBC抗体的细胞的细胞分化则由抑制性T淋巴细胞调节。