Gerber Pehuén Pereyra, Cabrini Mercedes, Jancic Carolina, Paoletti Luciana, Banchio Claudia, von Bilderling Catalina, Sigaut Lorena, Pietrasanta Lía I, Duette Gabriel, Freed Eric O, Basile Genevieve de Saint, Moita Catarina Ferreira, Moita Luis Ferreira, Amigorena Sebastian, Benaroch Philippe, Geffner Jorge, Ostrowski Matías
Instituto de Investigaciones Biomédicas en Retrovirus y Síndrome de Inmunodeficiencia Adquirida (INBIRS)-Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Universidad de Buenos Aires, C1121ABG Buenos Aires, Argentina.
Instituto de Medicina Experimental-CONICET, Academia Nacional de Medicina, C1425AUM Buenos Aires, Argentina.
J Cell Biol. 2015 May 11;209(3):435-52. doi: 10.1083/jcb.201409082. Epub 2015 May 4.
During the late stages of the HIV-1 replication cycle, the viral polyprotein Pr55(Gag) is recruited to the plasma membrane (PM), where it binds phosphatidylinositol 4,5-bisphosphate (PI(4,5)P2) and directs HIV-1 assembly. We show that Rab27a controls the trafficking of late endosomes carrying phosphatidylinositol 4-kinase type 2 α (PI4KIIα) toward the PM of CD4(+) T cells. Hence, Rab27a promotes high levels of PM phosphatidylinositol 4-phosphate and the localized production of PI(4,5)P2, therefore controlling Pr55(Gag) membrane association. Rab27a also controls PI(4,5)P2 levels at the virus-containing compartments of macrophages. By screening Rab27a effectors, we identified that Slp2a, Slp3, and Slac2b are required for the association of Pr55(Gag) with the PM and that Slp2a cooperates with Rab27a in the recruitment of PI4KIIα to the PM. We conclude that by directing the trafficking of PI4KIIα-positive endosomes toward the PM, Rab27a controls PI(4,5)P2 production and, consequently, HIV-1 replication.
在HIV-1复制周期的后期,病毒多聚蛋白Pr55(Gag)被招募到质膜(PM),在那里它结合磷脂酰肌醇4,5-二磷酸(PI(4,5)P2)并指导HIV-1组装。我们发现Rab27a控制携带磷脂酰肌醇4-激酶2α型(PI4KIIα)的晚期内体向CD4(+) T细胞质膜的运输。因此,Rab27a促进质膜磷脂酰肌醇4-磷酸的高水平以及PI(4,5)P2的局部产生,从而控制Pr55(Gag)与膜的结合。Rab27a还控制巨噬细胞含病毒区室的PI(4,5)P2水平。通过筛选Rab27a效应器,我们确定Slp2a、Slp3和Slac2b是Pr55(Gag)与质膜结合所必需的,并且Slp2a在将PI4KIIα招募到质膜的过程中与Rab27a协同作用。我们得出结论,通过引导PI4KIIα阳性内体向质膜的运输,Rab27a控制PI(4,5)P2的产生,进而控制HIV-1复制。