Walzer Thierry, Galibert Laurent, De Smedt Thibaut
Amgen Inc., Seattle, WA 98119, USA.
Eur J Immunol. 2005 Feb;35(2):391-8. doi: 10.1002/eji.200425669.
The poxvirus A39R protein is a member of the semaphorin family that binds to Plexin C1, a molecule expressed on neutrophils and dendritic cells (DC). We previously showed that binding of A39R to Plexin C1 induces local rearrangement of the actin cytoskeleton and inhibits integrin-mediated adhesion, leading to cell retraction. As phagocytosis is dependent on both cytoskeleton integrity and integrin function, we tested the effect of A39R on DC and neutrophil phagocytosis. We found that A39R treatment strongly inhibits phagocytosis by DC and neutrophils in vitro in a Plexin C1-dependent fashion. Moreover, A39R treatment inhibited the capacity of CD8alpha+ DC to take up apoptotic bodies in vivo. As a consequence, A39R impaired the ability of CD8alpha+ DC to cross-prime CD8+ T cells ex vivo. In contrast, A39R had no effect on direct priming of CD8+ T cells by peptide-pulsed CD8alpha+ DC in vitro. These results suggest that poxviruses may use semaphorin homologs as a means to evade the immune system.
痘病毒A39R蛋白是信号素家族的成员,可与Plexin C1结合,Plexin C1是一种在中性粒细胞和树突状细胞(DC)上表达的分子。我们之前表明,A39R与Plexin C1的结合会诱导肌动蛋白细胞骨架的局部重排,并抑制整合素介导的黏附,导致细胞回缩。由于吞噬作用依赖于细胞骨架完整性和整合素功能,我们测试了A39R对DC和中性粒细胞吞噬作用的影响。我们发现,A39R处理在体外以依赖Plexin C1的方式强烈抑制DC和中性粒细胞的吞噬作用。此外,A39R处理在体内抑制了CD8α+ DC摄取凋亡小体的能力。因此,A39R损害了CD8α+ DC在体外交叉启动CD8+ T细胞的能力。相比之下,A39R对肽脉冲的CD8α+ DC在体外直接启动CD8+ T细胞没有影响。这些结果表明,痘病毒可能利用信号素同源物作为逃避免疫系统的一种手段。