Tian Jun, Liu Li, Wang Xiangai, Sun Xuewu, Mu Suli, Wu Chuanjun, Han Maoqiang
Yantai Stomatological Hospital, Yantai, 264001, Shandong, China,
Inflammation. 2014 Dec;37(6):2013-9. doi: 10.1007/s10753-014-9933-y.
Invariant natural killer T (iNKT) cell is a critical element for both innate and adaptive immunity. The quick responses of mature iNKT cells to TCR stimulation require activation of several different signaling pathways. However, the roles of these signaling pathways in mature iNKT cell biology remain incompletely understood. To address this issue, single signaling pathway was blocked with inhibitor in iNKT cells, and the roles of these signaling pathways were estimated. Results showed that mammalian target of rapamycin (mTOR) plays an essential role for cytokine production and survival in iNKT cells. In contrast, ERK and JNK are more important for iNKT cell effector function, but not survival. Our findings delineate the distinct roles of different signaling pathways in mature iNKT cells and therefore shed new light for modulating iNKT cell function in disease conditions.
不变自然杀伤T(iNKT)细胞是先天性免疫和适应性免疫的关键组成部分。成熟iNKT细胞对TCR刺激的快速反应需要激活几种不同的信号通路。然而,这些信号通路在成熟iNKT细胞生物学中的作用仍未完全清楚。为了解决这个问题,用抑制剂阻断iNKT细胞中的单一信号通路,并评估这些信号通路的作用。结果表明,雷帕霉素靶蛋白(mTOR)在iNKT细胞的细胞因子产生和存活中起重要作用。相比之下,ERK和JNK对iNKT细胞的效应功能更重要,但对其存活不重要。我们的研究结果阐明了不同信号通路在成熟iNKT细胞中的不同作用,因此为在疾病状态下调节iNKT细胞功能提供了新的思路。