Implications for the role of cognate interactions in in vitro human B cell activation by Staphylococcus aureus Cowan I and pokeweed mitogen.
Implications for the role of cognate interactions in in vitro human B cell activation by Staphylococcus aureus Cowan I and pokeweed mitogen.
复制标题
金黄色葡萄球菌 Cowan I 和美洲商陆有丝分裂原在体外人 B 细胞激活中同源相互作用的作用的意义。
DOI:
10.1172/jci112290
复制
发表时间:
1986
期刊:
影响因子:
--
通讯作者:
T. Tsunematsu
中科院分区:
文献类型:
--
作者:
N. Suzuki;T. Sakane;Y. Ueda;Y. Murakawa;T. Tsunematsu
Human B cell-triggering mechanisms were investigated using the polyclonal activators Staphylococcus aureus Cowan I (SAC) and pokeweed mitogen (PWM). When the cultures of B cells, T cells, and monocytes were stimulated for 5 d by SAC or PWM, B cells could be activated by both mitogens to proliferate and secrete Ig. Even when T cells were substituted by T cell-derived soluble factors, SAC-stimulated B cells could differentiate into Ig-secreting cells. In contrast, interactions of B and T cells for at least the first 6 h of culture were necessary for the B cell triggering by PWM. Experiments that allow a more precise delineation of the B cell-triggering mechanisms by PWM demonstrated that interactions of B cells with T4+ but not T8+ cells are required for the B cell triggering; anti-Ia or anti-T4 antibody can block this triggering; in contrast, anti-T3 or anti-T8 antibody do not exert any effects on the B cell triggering. However, all these monoclonal antibodies could not modulate the ability of B cells that had been already activated by PWM to respond to T cell-derived factors. These data suggest that SAC can directly activate B cells, while cognate interactions between Ia-like antigens on B cells and T4+ cells are essential for B cell triggering by PWM. Furthermore, once B cells are triggered, they will proliferate, differentiate, and secrete Ig in response to T cell-derived factors; Ia-like antigens or T cell differentiation antigens may not be involved in the processes in this cascade.
DOI:
--
发表时间:
1983
期刊:
Journal of immunology (Baltimore, Md. : 1950)
影响因子:
--
作者:
Engleman,EG;Benike,CJ;Metzler,C;Gatenby,PA;Evans,RL
通讯作者:
Evans,RL
DOI:
--
发表时间:
1984
期刊:
Journal of immunology (Baltimore, Md. : 1950)
影响因子:
--
作者:
Puck,JM;Rich,RR
通讯作者:
Rich,RR