Meng Xiaobo, Kanwar Namita, Du Qiujiang, Goping Ing S, Bleackley R Chris, Wilkins John A
Manitoba Centre for Proteomics and Systems Biology, University of Manitoba, John Buhler Research Centre, Winnipeg, MB, Canada.
Eur J Immunol. 2009 Feb;39(2):552-60. doi: 10.1002/eji.200838474.
The NK immunological synapse (NKIS) is a dynamic structure dependent on the assembly of membrane, cytoskeletal and signaling components. These serve to focus and generate stimuli for adhesion and orientation of the cytoskeleton for targeted cytolytic granule release. Previous studies have demonstrated the importance of the cytoskeleton in these processes. We previously identified PPP1R9B (neurabin 2, spinophilin) as a cytoskeletal component of the NK-like cell line YTS. We demonstrate that (i) PPP1R9B gradually accumulates at the NKIS in a maturation stage-dependent manner; (ii) it mimics the early kinetics of actin recruitment to the NKIS but it precedes actin departure from the site; (iii) it is recruited by CD18 stimulation but not by CD28 ligation; (iv) it is required for the maintenance of the cortical F-actin organization in the YTS cells and knocking down PPP1R9B reduces the frequency of YTS-target cell conjugation, possibly due to the collapsed F-actin cytoskeleton in these cells. These results indicate that PPP1R9B is required for synapse formation in the NK cells and suggest that it may be involved in the maintenance of cellular architecture by regulation of actin assembly, possibly acting to stabilize the NKIS until granule release is eminent.
自然杀伤细胞免疫突触(NKIS)是一种动态结构,依赖于膜、细胞骨架和信号传导成分的组装。这些成分用于集中并产生刺激,以促进细胞骨架的黏附和定向,从而实现靶向溶细胞颗粒的释放。先前的研究已经证明了细胞骨架在这些过程中的重要性。我们之前鉴定出PPP1R9B(神经素2,亲肌蛋白)是自然杀伤样细胞系YTS的一种细胞骨架成分。我们证明:(i)PPP1R9B以成熟阶段依赖性方式逐渐在NKIS处积累;(ii)它模拟了肌动蛋白募集到NKIS的早期动力学,但在肌动蛋白离开该位点之前;(iii)它通过CD18刺激被募集,但不通过CD28连接被募集;(iv)它是维持YTS细胞中皮质F-肌动蛋白组织所必需的,敲低PPP1R9B会降低YTS与靶细胞结合的频率,这可能是由于这些细胞中F-肌动蛋白细胞骨架的塌陷。这些结果表明,PPP1R9B是自然杀伤细胞突触形成所必需的,并表明它可能通过调节肌动蛋白组装参与细胞结构的维持,可能起到稳定NKIS直至颗粒释放显著的作用。