Lettesjö H, Möller E
Department of Immunology, Arrhenius Laboratories for Natural Sciences, Stockholm University, Sweden.
Scand J Immunol. 1997 Jan;45(1):43-9. doi: 10.1046/j.1365-3083.1997.d01-373.x.
Rheumatoid arthritis synovial fluid (RA-SF) contains a factor that induces IgG2b antibody production in LPS-stimulated murine B cells and therefore is called IgG2b inducing factor (IgG2bIF). When LPS, together with crude RA-SF or semi-purified IgG2bIF, was added to highly purified LPS-stimulated B cells, the number of IgG2b-producing cells was substantially enhanced. This shows that IgG2bIF acts directly on activated B cells, presumably by binding to a receptor expressed on LPS-activated B cells. In vivo LPS-activated B blasts were not able to respond to RA-SF unless LPS was present in vitro, showing that LPS is needed to maintain cell viability and responsiveness to the IgG2bIF. To elucidate the mechanism for the IgG2bIF effect on highly purified B cells, the IgG2b response of LPS-stimulated, Bruton's tyrosine kinase-defective, xidB blasts was studied. Purified B blasts from the btk-defective CBA/N mouse strain were sensitive to IgG2bIF. These findings show that IgG2bIF acts directly on B cells and activates cells through a btk-independent pathway.
类风湿性关节炎滑液(RA - SF)含有一种能在脂多糖(LPS)刺激的小鼠B细胞中诱导IgG2b抗体产生的因子,因此被称为IgG2b诱导因子(IgG2bIF)。当将LPS与粗制RA - SF或半纯化的IgG2bIF一起添加到高度纯化的LPS刺激的B细胞中时,产生IgG2b的细胞数量显著增加。这表明IgG2bIF直接作用于活化的B细胞,推测是通过与LPS活化的B细胞上表达的受体结合。体内LPS活化的B母细胞除非体外存在LPS,否则无法对RA - SF作出反应,这表明LPS是维持细胞活力和对IgG2bIF反应性所必需的。为了阐明IgG2bIF对高度纯化B细胞的作用机制,研究了LPS刺激的、布鲁顿酪氨酸激酶缺陷的xidB母细胞的IgG2b反应。来自btk缺陷的CBA/N小鼠品系的纯化B母细胞对IgG2bIF敏感。这些发现表明IgG2bIF直接作用于B细胞,并通过不依赖btk的途径激活细胞。