Riol-Blanco Lorena, Delgado-Martín Cristina, Sánchez-Sánchez Noelia, Alonso-C Luis M, Gutiérrez-López María Dolores, Del Hoyo Gloria Martínez, Navarro Joaquín, Sánchez-Madrid Francisco, Cabañas Carlos, Sánchez-Mateos Paloma, Rodríguez-Fernández José Luis
Centro de Investigaciones Biológicas, Consejo Superior de Investigaciones Científicas, Madrid, Spain.
Nat Immunol. 2009 Jul;10(7):753-60. doi: 10.1038/ni.1750. Epub 2009 Jun 7.
The immunological synapse (IS) is a cell-cell junction formed between CD4(+) T cells and dendritic cells (DCs). Here we show in vitro and in vivo that IS formation inhibits apoptosis of DCs. Consistent with these results, IS formation induced antiapoptotic signaling events, including activation of the kinase Akt1 and localization of the prosurvival transcription factor NF-kappaB and the proapoptotic transcription factor FOXO1 to the nucleus and cytoplasm, respectively. Inhibition of phosphatidylinositol 3-OH kinase and Akt1 partially prevented the antiapoptotic effects of IS formation. Direct stimulation of the IS component CD40 on DCs leads to the activation of Akt1, suggesting the involvement of this receptor in the antiapoptotic effects observed upon IS formation.
免疫突触(IS)是在CD4(+) T细胞和树突状细胞(DC)之间形成的细胞间连接。我们在此证明,在体外和体内,IS的形成均可抑制DC的凋亡。与这些结果一致,IS的形成诱导了抗凋亡信号事件,包括激酶Akt1的激活以及促生存转录因子NF-κB和促凋亡转录因子FOXO1分别定位于细胞核和细胞质。抑制磷脂酰肌醇3-OH激酶和Akt1可部分阻止IS形成的抗凋亡作用。直接刺激DC上的IS成分CD40可导致Akt1的激活,这表明该受体参与了IS形成时所观察到的抗凋亡作用。