Department of Cancer Immunology and AIDS, Dana-Farber Cancer Institute, Boston, MA 02115, USA.
Proc Natl Acad Sci U S A. 2010 Feb 9;107(6):2556-61. doi: 10.1073/pnas.0913671107. Epub 2010 Jan 25.
Trafficking of transmembrane receptors to a specific intracellular compartment is conducted by adaptor molecules that bind to target motifs within the cytoplasmic domains of cargo proteins. We generated mice containing a lymphoid-specific deficiency of AP-1 using RNAi knockdown technology. Inhibition of AP-1 expression in thymocytes blocks progression from double-positive immature thymocytes, resulting in complete absence of CD4(+) single-positive thymocytes and severe reduction of CD3(+)CD8(+) single-positive thymocytes. Analysis of the contribution of AP-1 deficiency on the interaction between mature CD4(+) T cells and antigen-presenting cells revealed that AP-1 is essential to efficient immune synapse formation and associated T cell activation, suggesting a possible mechanism of AP-1 function in thymocyte development.
跨膜受体向特定细胞内隔室的运输是由衔接分子介导的,这些分子与货物蛋白胞质结构域中的靶基序结合。我们使用 RNAi 敲低技术生成了淋巴特异性缺乏 AP-1 的小鼠。在胸腺细胞中抑制 AP-1 的表达会阻止双阳性未成熟胸腺细胞的进展,导致 CD4(+)单阳性胸腺细胞完全缺失和 CD3(+)CD8(+)单阳性胸腺细胞严重减少。分析 AP-1 缺乏对成熟 CD4(+)T 细胞与抗原呈递细胞相互作用的影响表明,AP-1 对于有效免疫突触形成和相关 T 细胞激活是必需的,这表明了 AP-1 在胸腺细胞发育中的功能的一种可能机制。