Dearden-Badet M T, Revillard J P
Laboratory of Immunology, INSERM U80, Hôpital E. Herriot, Lyons, France.
Immunology. 1993 Dec;80(4):658-60.
Bacterial lipopolysaccharide (LPS) induces a strong B-cell proliferative response with subsequent differentiation, through a complex signal transduction pathway. This process is known to be mediated through protein kinase C (PKC) translocation without Ca2+ mobilization. Here, we show that B-cell proliferative responses induced by five different LPS preparations, as well as by F(ab')2 anti-IgM antibodies, are inhibited by the tyrosine kinase inhibitors, genistein and herbimycin A. In contrast, B-cell proliferation induced by the combination of phorbol 12-myristate 13-acetate (PMA) plus ionomycin was not influenced by treatment with either herbimycin A or genistein. These data indicate that tyrosine phosphorylation is required to initiate B-cell proliferation by LPS.
细菌脂多糖(LPS)通过复杂的信号转导途径诱导强烈的B细胞增殖反应并随后分化。已知该过程是通过蛋白激酶C(PKC)易位介导的,而无Ca2+动员。在此,我们表明,酪氨酸激酶抑制剂染料木黄酮和赫曲霉素A可抑制由五种不同的LPS制剂以及F(ab')2抗IgM抗体诱导的B细胞增殖反应。相反,佛波醇12-肉豆蔻酸酯13-乙酸酯(PMA)加离子霉素联合诱导的B细胞增殖不受赫曲霉素A或染料木黄酮处理的影响。这些数据表明,酪氨酸磷酸化是LPS启动B细胞增殖所必需的。