Fooksman David Robert, Shaikh Saame Raza, Boyle Sarah, Edidin Michael
Department of Biology, Johns Hopkins University, Baltimore, MD 21218, USA.
J Immunol. 2009 May 1;182(9):5179-82. doi: 10.4049/jimmunol.0801797.
Little is known about the signaling that occurs in an APC during contact with a T cell. In this article we report the concentration of the signaling lipid phosphatidylinositol 4,5-bisphosphate (PI(4,5)P(2)) at the APC side of the immunological synapse. In both human and mouse cells, a PI(4,5)P(2)-specific fluorescent reporter, PH-GFP (where PH is pleckstrin homology), detected an Ag-dependent enrichment of PI(4,5)P(2) at the synapse between Ag-specific T cells and APC. When PIP(4,5)P(2) was sequestered by a high concentration of PH-GFP reporter, cells were less susceptible to CTL-mediated lysis than control cells. These findings suggest a new regulatory target for modulating immune function that may be exploited for immune escape by pathogens and tumors.
关于抗原呈递细胞(APC)与T细胞接触过程中发生的信号传导,人们了解甚少。在本文中,我们报道了免疫突触APC一侧信号脂质磷脂酰肌醇4,5-二磷酸(PI(4,5)P(2))的浓度。在人类和小鼠细胞中,一种PI(4,5)P(2)特异性荧光报告分子PH-GFP(其中PH是普列克底物蛋白同源结构域),检测到在抗原特异性T细胞与APC之间的突触处,PI(4,5)P(2)呈抗原依赖性富集。当PI(4,5)P(2)被高浓度的PH-GFP报告分子隔离时,细胞比对照细胞更不易受到细胞毒性T淋巴细胞(CTL)介导的裂解作用。这些发现提示了一个调节免疫功能的新调控靶点,病原体和肿瘤可能利用该靶点实现免疫逃逸。