IL-3 augments TCR-mediated responses of type 2 CD4 T cells.
IL-3 augments TCR-mediated responses of type 2 CD4 T cells.
复制标题
IL-3 增强 2 型 CD4 T 细胞的 TCR 介导的反应。
DOI：
10.4049/jimmunol.156.1.27
复制
发表时间：
1996
影响因子：
4.4
通讯作者：
Y. Asano
中科院分区：
文献类型：
--
作者：
Y. Dan;Y. Katakura;A. Ametani;S. Kaminogawa;Y. Asano
A subset of type 2, but not type 1, CD4 T cell clones expresses IL-3R and can be stimulated by IL-3. Expression of IL-3R on these type 2 T cell clones is induced by TCR stimulation, and subsequent stimulation by IL-3 augmented the proliferation of and IL-4 production by these cells. This augmented response is inhibited by anti-IL-4 mAb, suggesting the involvement of IL-4 in this response. In place of TCR stimulation, treatment of these type 2 CD4 T cell clones with PMA rendered them responsive to further stimulation of proliferation by IL-3, indicating the cooperation between the IL-3R-elicited signals and PKC-mediated signals in stimulating proliferation. Although the augmentation of the TCR-mediated proliferative response by IL-3 was mainly due to the increased production of IL-4, we also demonstrated the presence of IL-4-independent mechanism mediating the response to IL-3. In situ, we found that splenic T cells could be induced to respond to Il-3 by TCR stimulation. Thus, IL-3 can stimulate a specific population of T cells and influence the immune response.
