Sultzer B M, Bandekar J R, Castagna R, Abu-Lawi K, Sadeghian M, Norin A J
Department of Microbiology and Immunology, State University of New York Health Science Center, Brooklyn 11203.
Infect Immun. 1992 Sep;60(9):3533-8. doi: 10.1128/iai.60.9.3533-3538.1992.
Earlier studies in our laboratory showed that the lipopolysaccharide (LPS) of Salmonella typhi, which fails to activate B lymphocytes of C3H/HeJ mice, can suppress proliferation and polyclonal antibody synthesis by these cells when they are stimulated by polyclonal activators. In order to determine what stage of the cell cycle was blocked, resting B cells from C3H/HeJ spleens were activated by using different mitogens in the presence of inhibitory concentrations of LPS and analyzed by flow cytometry, using acridine orange to stain DNA and RNA. LPS was found to inhibit the progression of cells into the G1 stage of the cell cycle. Furthermore, [3H]uridine uptake studies showed that RNA synthesis is inhibited during the early phase of activation. These results indicate that inhibition by LPS of the signalling process occurs during a critical period of the cell cycle when the cells become susceptible to the inhibitory effects of LPS. To examine whether LPS acts only on B cells or whether it can suppress other immunocompetent cells from C3H/HeJ mice, studies were carried out on activated thymocytes and macrophages. LPS was found to inhibit thymocyte proliferation stimulated by concanavalin A or the combination of phorbol myristate acetate and ionomycin. Prostaglandin E2 synthesis by macrophages was also blocked by LPS. Thus, LPS is a potent inhibitor of the functioning of the major immunocompetent cells of C3H/HeJ mice.
我们实验室早期的研究表明,伤寒沙门氏菌的脂多糖(LPS)不能激活C3H/HeJ小鼠的B淋巴细胞,但当这些细胞受到多克隆激活剂刺激时,它能抑制这些细胞的增殖和多克隆抗体合成。为了确定细胞周期的哪个阶段被阻断,在存在抑制浓度LPS的情况下,使用不同的有丝分裂原激活来自C3H/HeJ脾脏的静止B细胞,并通过流式细胞术进行分析,使用吖啶橙对DNA和RNA进行染色。发现LPS抑制细胞进入细胞周期的G1期。此外,[3H]尿苷摄取研究表明,在激活的早期阶段RNA合成受到抑制。这些结果表明,LPS对信号传导过程的抑制发生在细胞周期的关键时期,此时细胞变得易受LPS抑制作用的影响。为了研究LPS是否仅作用于B细胞,或者它是否能抑制来自C3H/HeJ小鼠的其他免疫活性细胞,对活化的胸腺细胞和巨噬细胞进行了研究。发现LPS抑制伴刀豆球蛋白A或佛波酯和离子霉素组合刺激的胸腺细胞增殖。LPS也阻断了巨噬细胞合成前列腺素E2。因此,LPS是C3H/HeJ小鼠主要免疫活性细胞功能的有效抑制剂。