Khan Mélissa Erin, Borde Chloé, Rocha Eduardo P C, Mériaux Véronique, Maréchal Vincent, Escoll Pedro, Goyard Sophie, Cavaillon Jean-Marc, Manoury Bénédicte, Doyen Noëlle
Institut Pasteur, Département Infection et Epidémiologie, Unité Cytokines & Inflammation, Paris, France.
Institut Pasteur, Département Génomes et Génétique, Unité de Génomique Evolutive des Microbes, Paris, France; CNRS UMR3525, Paris, France.
PLoS Negl Trop Dis. 2014 Nov 13;8(11):e3308. doi: 10.1371/journal.pntd.0003308. eCollection 2014 Nov.
DNA sequences purified from distinct organisms, e.g. non vertebrate versus vertebrate ones, were shown to differ in their TLR9 signalling properties especially when either mouse bone marrow-derived- or human dendritic cells (DCs) are probed as target cells. Here we found that the DC-targeting immunostimulatory property of Leishmania major DNA is shared by other Trypanosomatidae DNA, suggesting that this is a general trait of these eukaryotic single-celled parasites. We first documented, in vitro, that the low level of immunostimulatory activity by vertebrate DNA is not due to its limited access to DCs' TLR9. In addition, vertebrate DNA inhibits the activation induced by the parasite DNA. This inhibition could result from the presence of competing elements for TLR9 activation and suggests that DNA from different species can be discriminated by mouse and human DCs. Second, using computational analysis of genomic DNA sequences, it was possible to detect the presence of over-represented inhibitory and under-represented stimulatory sequences in the vertebrate genomes, whereas L. major genome displays the opposite trend. Interestingly, this contrasting features between L. major and vertebrate genomes in the frequency of these motifs are shared by other Trypanosomatidae genomes (Trypanosoma cruzi, brucei and vivax). We also addressed the possibility that proteins expressed in DCs could interact with DNA and promote TLR9 activation. We found that TLR9 is specifically activated with L. major HMGB1-bound DNA and that HMGB1 preferentially binds to L. major compared to mouse DNA. Our results highlight that both DNA sequence and vertebrate DNA-binding proteins, such as the mouse HMGB1, allow the TLR9-signaling to be initiated and achieved by Trypanosomatidae DNA.
从不同生物体中纯化得到的DNA序列,例如非脊椎动物与脊椎动物的DNA序列,已显示出其Toll样受体9(TLR9)信号传导特性存在差异,尤其是当以小鼠骨髓来源的树突状细胞或人树突状细胞(DCs)作为靶细胞进行检测时。在此,我们发现利什曼原虫主要DNA的靶向DCs的免疫刺激特性也存在于其他锥虫科DNA中,这表明这是这些真核单细胞寄生虫的一个普遍特征。我们首先在体外证明,脊椎动物DNA的低水平免疫刺激活性并非因其难以接触DCs的TLR9。此外,脊椎动物DNA会抑制寄生虫DNA诱导的激活。这种抑制可能是由于存在与TLR9激活竞争的元件,这表明小鼠和人DCs能够区分来自不同物种的DNA。其次,通过对基因组DNA序列的计算分析,有可能检测到脊椎动物基因组中存在过度表达的抑制性序列和表达不足的刺激性序列,而利什曼原虫主要基因组则呈现相反的趋势。有趣的是,利什曼原虫主要基因组与脊椎动物基因组在这些基序频率上的这种对比特征也存在于其他锥虫科基因组(克氏锥虫、布氏锥虫和间日锥虫)中。我们还探讨了DCs中表达的蛋白质是否可能与DNA相互作用并促进TLR9激活的可能性。我们发现TLR9会被与利什曼原虫主要高迁移率族蛋白B1(HMGB1)结合的DNA特异性激活,并且与小鼠DNA相比,HMGB1更倾向于结合利什曼原虫主要DNA。我们的结果突出表明,DNA序列以及脊椎动物DNA结合蛋白,如小鼠HMGB1,都能使锥虫科DNA启动并实现TLR9信号传导。