Lindsberg M L, Brunswick M, Keegan A, Mond J J
Department of Medicine, Uniformed Services University of the Health Sciences, Bethesda, Maryland 20814-4799.
Cell Immunol. 1990 Oct 15;130(2):320-8. doi: 10.1016/0008-8749(90)90275-v.
The experiments in this manuscript confirm and extend our previous finding that IL4 has minimal enhancing activity on B cell activation stimulated by anti-Ig-dextran conjugates. The absence of significant IL4-mediated enhancement is seen also under conditions which are limiting for optimal B cell proliferation. Thus, even when B cells are cultured at low cell densities where cell to cell contact is minimized and are stimulated with picogram per milliliter concentrations of anti-Ig-dextran, IL4 mediates low levels of enhanced proliferation, if at all. The low level of IL4-induced enhancement does not reflect the anti-Ig-dextran-mediated downregulation of IL4 receptors on B cells, since anti-Ig-dextran stimulates an increase in IL4 receptors similar in magnitude to that stimulated by IL4 by itself. To exclude the possibility that anti-Ig-dextran was stimulating IL4 secretion by B cells and thus masking an effect of added IL4, we added inhibiting concentrations of monoclonal anti-IL4 antibody, with the B cells and found that it was without effect on anti-Ig-dextran-stimulated proliferation. Our results suggest that IL4 may not have a prominent role in influencing B cell growth that is stimulated by multivalent T cell-independent antigens.
本手稿中的实验证实并扩展了我们之前的发现,即白细胞介素4(IL4)对由抗Ig-葡聚糖缀合物刺激的B细胞活化具有最小的增强活性。在限制最佳B细胞增殖的条件下,也观察到没有显著的IL4介导的增强作用。因此,即使B细胞以低细胞密度培养,使细胞间接触最小化,并以每毫升皮克浓度的抗Ig-葡聚糖刺激,IL4介导的增殖增强水平也很低(如果有增强的话)。IL4诱导的低水平增强并不反映抗Ig-葡聚糖介导的B细胞上IL4受体的下调,因为抗Ig-葡聚糖刺激的IL4受体增加幅度与IL4自身刺激的幅度相似。为了排除抗Ig-葡聚糖刺激B细胞分泌IL4从而掩盖添加IL4的作用的可能性,我们加入抑制浓度的单克隆抗IL4抗体与B细胞一起培养,发现它对抗Ig-葡聚糖刺激的增殖没有影响。我们的结果表明,IL4在影响由多价非T细胞依赖性抗原刺激的B细胞生长方面可能没有突出作用。