Shinohara Hisaaki, Yamasaki Sho, Maeda Shiori, Saito Takashi, Kurosaki Tomohiro
Laboratory for Lymphocyte Differentiation, RIKEN Research Center for Allergy and Immunology, Yokohama, Kanagawa, Japan.
Int Immunol. 2009 Apr;21(4):393-401. doi: 10.1093/intimm/dxp007. Epub 2009 Feb 17.
The serine/threonine kinase MEKK3, also known as mitogen-activated protein kinase kinase kinase 3, is a critical activator of the transcription factor NF-kappaB in innate immunity. However, the physiological function of MEKK3 in adaptive immunity is unclear. Here we report that following TCR signaling, MEKK3 positively regulated the kinase, IkappaB kinase, leading to NF-kappaB activation. T cells lacking MEKK3 were defective in TCR-induced and cytokine-induced responses. Furthermore, T cell-specific deletion of MEKK3 resulted in reduced numbers of thymocytes and peripheral T cells. Thus, our results provide genetic evidence that MEKK3 plays a crucial role in adaptive immunity.
丝氨酸/苏氨酸激酶MEKK3,也被称为丝裂原活化蛋白激酶激酶激酶3,是天然免疫中转录因子NF-κB的关键激活因子。然而,MEKK3在适应性免疫中的生理功能尚不清楚。在此我们报告,在TCR信号传导后,MEKK3正向调节激酶IκB激酶,导致NF-κB激活。缺乏MEKK3的T细胞在TCR诱导和细胞因子诱导的反应中存在缺陷。此外,MEKK3的T细胞特异性缺失导致胸腺细胞和外周T细胞数量减少。因此,我们的结果提供了遗传学证据,表明MEKK3在适应性免疫中起关键作用。