Leanderson T, Forni L
Eur J Immunol. 1984 Nov;14(11):1016-21. doi: 10.1002/eji.1830141110.
Over a wide range of concentrations affinity-purified rabbit anti-mouse mu chain antibodies, or their F(ab')2 fragments, inhibit the appearance of immunoglobulin-secreting cells (plaque-forming cells; PFC) in lipopolysaccharide-stimulated murine spleen cell cultures without affecting proliferation. Both IgM and IgG PFC are inhibited although the number of blasts bearing surface IgG remains unaltered. The IgM and IgG PFC response could be reconstituted to normal levels in cell cultures suppressed by mu-specific antibodies by the addition of supernatants from in vitro propagated helper T cell clones, or from EL4 lymphoma cells induced with phorbol ester. Interleukin 1-containing P388 supernatant, or recombinant DNA-derived murine interferon-gamma, did not reconstitute the PFC response in cell cultures suppressed by mu-specific antibodies, indicating that other factors are responsible for these effects. When spleen cell cultures, pre-activated with either lipopolysaccharide or monoclonal mouse mu-specific antibodies coupled to Sepharose, were exposed to EL4 supernatants in the presence of soluble mu-specific antibodies, maturation to secretion was inhibited while proliferation was not. The implications of these findings on assay systems for B cell growth and maturation factors are discussed.
在广泛的浓度范围内,亲和纯化的兔抗小鼠μ链抗体或其F(ab')2片段可抑制脂多糖刺激的小鼠脾细胞培养物中免疫球蛋白分泌细胞(噬斑形成细胞;PFC)的出现,而不影响细胞增殖。尽管携带表面IgG的母细胞数量未改变,但IgM和IgG PFC均受到抑制。通过添加体外增殖的辅助性T细胞克隆或佛波酯诱导的EL4淋巴瘤细胞的上清液,可使被μ特异性抗体抑制的细胞培养物中的IgM和IgG PFC反应恢复到正常水平。含白细胞介素1的P388上清液或重组DNA衍生的小鼠干扰素-γ不能使被μ特异性抗体抑制的细胞培养物中的PFC反应恢复,这表明其他因素对这些效应起作用。当用脂多糖或偶联到琼脂糖珠上的单克隆小鼠μ特异性抗体预先激活的脾细胞培养物在可溶性μ特异性抗体存在下暴露于EL4上清液时,细胞向分泌的成熟过程受到抑制,而增殖不受影响。本文讨论了这些发现对B细胞生长和成熟因子检测系统的意义。