Guangdong Laboratory for Lingnan Modern Agriculture, Laboratory of Insect Molecular Biology and Biotechnology, Guangdong Provincial Key Laboratory of Agro-Animal Genomics and Molecular Breeding, College of Animal Science, South China Agricultural University, 510642 Guangzhou, China.
Guangdong Provincial Key Laboratory of Insect Developmental Biology and Applied Technology, Institute of Insect Science and Technology, School of Life Sciences, South China Normal University, 510631 Guangzhou, China.
Proc Natl Acad Sci U S A. 2021 May 11;118(19). doi: 10.1073/pnas.2103021118.
Toll/Toll-like receptors (TLRs) are key regulators of the innate immune system in both invertebrates and vertebrates. However, while mammalian TLRs directly recognize pathogen-associated molecular patterns, the insect Toll pathway is thought to be primarily activated by binding Spätzle cytokines that are processed from inactive precursors in response to microbial infection. Phylogenetic and structural data generated in this study supported earlier results showing that Toll9 members differ from other insect Tolls by clustering with the mammalian TLR4 group, which recognizes lipopolysaccharide (LPS) through interaction with myeloid differentiation-2 (MD-2)-like proteins. Functional experiments showed that BmToll9 from the silkmoth also recognized LPS through interaction with two MD-2-like proteins, previously named BmEsr16 and BmPP, that we refer to in this study as BmMD-2A and BmMD-2B, respectively. A chimeric BmToll9-TLR4 receptor consisting of the BmToll9 ectodomain and mouse TLR4 transmembrane and Toll/interleukin-1 (TIR) domains also activated LPS-induced release of inflammatory factors in murine cells but only in the presence of BmMD-2A or BmMD-2B. Overall, our results indicate that BmToll9 is a pattern recognition receptor for LPS that shares conserved features with the mammalian TLR4-MD-2-LPS pathway.
Toll/Toll 样受体 (TLRs) 是无脊椎动物和脊椎动物固有免疫系统的关键调节因子。然而,虽然哺乳动物 TLR 直接识别病原体相关分子模式,但昆虫 Toll 途径被认为主要通过与 Spätzle 细胞因子结合而被激活,这些细胞因子在微生物感染时从无活性前体中被加工而来。本研究中生成的系统发育和结构数据支持了早期的结果,表明 Toll9 成员通过与识别脂多糖 (LPS) 的哺乳动物 TLR4 组聚类而与其他昆虫 Toll 不同,该组通过与髓样分化-2 (MD-2)-样蛋白相互作用来识别 LPS。功能实验表明,来自家蚕的 BmToll9 也通过与两个 MD-2 样蛋白(先前称为 BmEsr16 和 BmPP)相互作用来识别 LPS,我们在本研究中将其分别称为 BmMD-2A 和 BmMD-2B。由 BmToll9 胞外域和小鼠 TLR4 跨膜和 Toll/白细胞介素-1 (TIR) 域组成的嵌合 BmToll9-TLR4 受体也能激活 LPS 诱导的炎性因子在小鼠细胞中的释放,但仅在存在 BmMD-2A 或 BmMD-2B 的情况下。总体而言,我们的研究结果表明,BmToll9 是 LPS 的模式识别受体,与哺乳动物 TLR4-MD-2-LPS 途径具有保守特征。