Department of Laboratory Medicine and Pathology, The Cancer Center, University of Minnesota, Minneapolis, MN 55455, USA.
J Immunol. 2010 Apr 15;184(8):4074-7. doi: 10.4049/jimmunol.0903933. Epub 2010 Mar 12.
Regulatory T cell (Treg) development proceeds via a two-step process in which naive CD4(+) thymocytes are first converted into CD4(+)CD25(+)CD122(+)GITR(+)Foxp3(-) Treg progenitors, followed by a second step in which IL-2 converts these Treg progenitors into CD4(+)Foxp3(+) Tregs. The costimulatory molecule CD28 is required for efficient Treg development. However, the stage at which CD28 affects Treg development remains undefined. In this article, we demonstrate that Cd28(-/-) mice lack Treg progenitors. Furthermore, the P(187)YAP motif in the cytoplasmic tail of CD28, which links CD28 to Lck activation, is required for this process. In contrast, the Y(170)MNM motif, which links CD28 to PI3K activation, is not required for Treg progenitor development. Finally, the CD28/Lck pathway was shown to activate the NF-kappaB family of transcription factors. We demonstrate that c-Rel, but not NF-kappaB1, promotes the development of Treg progenitors. Thus, a CD28/c-Rel-dependent pathway is involved in initiating Treg development.
调节性 T 细胞(Treg)的发育是通过两步过程进行的,首先,幼稚 CD4(+)胸腺细胞首先转化为 CD4(+)CD25(+)CD122(+)GITR(+)Foxp3(-)Treg 前体细胞,然后第二步,IL-2 将这些 Treg 前体细胞转化为 CD4(+)Foxp3(+)Tregs。共刺激分子 CD28 是 Treg 发育所必需的。然而,CD28 影响 Treg 发育的阶段仍未定义。在本文中,我们证明 Cd28(-/-) 小鼠缺乏 Treg 前体细胞。此外,CD28 细胞质尾部的 P(187)YAP 基序将 CD28 与 Lck 激活连接起来,对于这个过程是必需的。相比之下,将 CD28 与 PI3K 激活连接起来的 Y(170)MNM 基序对于 Treg 前体细胞的发育不是必需的。最后,CD28/Lck 途径被证明可以激活 NF-kappaB 转录因子家族。我们证明 c-Rel,但不是 NF-kappaB1,促进了 Treg 前体细胞的发育。因此,CD28/c-Rel 依赖性途径参与启动 Treg 发育。