Figure 2 Western blot analysis for phosphorylation of important molecules of PI3K/AKT pathway. BCBL-1 cells were infected with Mock (M) or HSV-1 (H) for 12, 24, and 48 h. Cells were collected and cell lysates were subjected to SGC-CBP30 ic50 SDS-PAGE, transferred to membrane, and then immunoblotted with the indicated antibodies. To examine whether PI3K/AKT pathway was involved in KSHV lytic cycle replication by HSV-1, PI3K-specific inhibitor LY294002
was first used. RT-qPCR demonstrated that ORF26 mRNA in HSV-1-infected BCBL-1 cells pretreated with LY294002 was decreased 3.27-fold at 12 h, 3.64-fold at 24 h, and 2.81-fold at 48 h post infection of HSV-1, respectively, compared to HSV-1-infected BCBL-1 cells pretreated with DMSO (Figure 3A). To confirm this result, Western blot analysis
was performed. We found that pretreatment of LY294002 inactivated the downstream kinase AKT and reduced the expression of KSHV vIL-6 proteins (Figure 3B). Next, PI3K-DN, the dominant negative form of PI3K, was transfected to BCBL-1 cells followed by HSV-1 infection. As shown in Figure 3C, control plasmid pSG5 alone did not affect KSHV activation by HSV-1, but transfection of PI3K-DN decreased HSV-1-induced KSHV Rta and vIL-6 Cilengitide research buy expression. Finally, AKT-DN, the dominant negative form of AKT, was transfected to BCBL-1 cells followed by HSV-1 infection. Western blot analysis demonstrated that transfection of control plasmid pSRα alone did not influence
KSHV replication, but transfection of AKT-DN down-regulated the proteins expression of KSHV Rta and vIL-6 (Figure 4A). The results from IFA also indicated that transfection of AKT-DN significantly decreased HSV-1-induced KSHV ORF59 proteins expression (Figure 4B and 4C). These data suggest that activation of PI3K/AKT pathway involves in HSV-1-induced KSHV replication. Figure 3 Inhibition of PI3K suppresses HSV-1-induced reactivation of KSHV. (A) RT-qPCR was used to detect relative quantities of ORF26 mRNA in LY294002 or DMSO control pretreated and HSV-1 infected BCBL-1 cells as indicated. ** p < 0.01 and *** p < 0.001 for Student's t-test versus Mock Y-27632 cell line + DMSO group; ## p < 0.01 for Student’s t-test versus HSV-1 + DMSO group. (B) Western blot analysis was used to detect the expression of KSHV vIL-6 and phosphorylated AKT in LY294002 or DMSO pretreated and HSV-1 infected BCBL-1 cells as indicated. (C) Western blot analysis was used to detect the expression of KSHV Rta, vIL-6 and phosphorylated GSK-3β in PI3K-DN or control vector transfected and HSV-1 infected BCBL-1 cells as indicated. Figure 4 Inhibition of AKT suppresses HSV-1-induced reactivation of KSHV. (A) Western blot analysis was used to detect the expression of KSHV Rta and vIL-6 in AKT-DN or control vector transfected and HSV-1 infected BCBL-1 cells as indicated.