Bertin Samuel, Pierrefite-Carle Valérie
INSERM, Unité 638, Nice, France.
Autophagy. 2008 Nov;4(8):1086-9. doi: 10.4161/auto.7138. Epub 2008 Nov 6.
In addition to its clean-up function, autophagy is considered as an innate immunity mechanism due to its role in the removal of intracellular pathogens. Toll-like receptors (TLRs) are crucial components of innate immunity involved in the recognition of a diverse array of microbial products. Recent works demonstrated that different pathogen-associated molecular patterns (PAMPs) such as lipopolysaccharide (LPS) and single-strand RNA are able to induce autophagy via different TLRs in immune cells. In a recent report, we showed that bacterial CpG motifs, another PAMP, can induce autophagy in rodent and human tumor cell lines and that this process is TLR9-dependent. In addition, an increase in the number of autophagosomes can also be observed in vivo after the intratumoral injection of CpG motifs. These results extend the link between TLRs and autophagy to non-immune tumor cells and may be relevant for cancer treatment and more generally for gene therapy approaches in TLR9-positive tissues. In this addendum, we discuss the potential mechanisms and the consequences of the CpG-induced autophagy in tumor cells.
除了其清除功能外,自噬因其在清除细胞内病原体中的作用而被视为一种先天免疫机制。Toll样受体(TLRs)是先天免疫的关键组成部分,参与识别多种微生物产物。最近的研究表明,不同的病原体相关分子模式(PAMPs),如脂多糖(LPS)和单链RNA,能够通过免疫细胞中的不同TLRs诱导自噬。在最近的一份报告中,我们表明细菌CpG基序,另一种PAMP,可在啮齿动物和人类肿瘤细胞系中诱导自噬,且该过程依赖于TLR9。此外,在瘤内注射CpG基序后,体内也可观察到自噬体数量增加。这些结果将TLRs与自噬之间的联系扩展到非免疫肿瘤细胞,可能与癌症治疗相关,更广泛地说,与TLR9阳性组织中的基因治疗方法相关。在本附录中,我们讨论了CpG诱导的肿瘤细胞自噬的潜在机制和后果。