Graduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, South Korea.
Department of Systems Biology, College of Life Science and Biotechnology, Yonsei University, Seoul, South Korea.
Front Immunol. 2022 Jul 7;13:875083. doi: 10.3389/fimmu.2022.875083. eCollection 2022.
Toll-like receptors (TLRs) play critical roles in the first line of host defense against pathogens through recognition of pathogen-associated molecular patterns and initiation of the innate immune responses. The proper localization of TLRs in specific subcellular compartments is crucial for their ligand recognition and downstream signaling to ensure appropriate responses against pathogens while avoiding erroneous or excessive activation. Several TLRs, including TLR7 and TLR9 but not TLR4, depend on UNC93B1 for their proper intracellular localization and signaling. Accumulating evidence suggest that UNC93B1 differentially regulates its various client TLRs, but the specific mechanisms by which UNC93B1 controls individual TLRs are not well understood. Protein N-glycosylation is one of the most frequent and important post-translational modification that occurs in membrane-localized or secreted proteins. UNC93B1 was previously shown to be glycosylated at Asn251 and Asn272 residues. In this study, we investigated whether N-glycosylation of UNC93B1 affects its function by comparing wild type and glycosylation-defective mutant UNC93B1 proteins. It was found that glycosylation of Asn251 and Asn272 residues can occur independently of each other and mutation of neither N251Q or N272Q in UNC93B1 altered expression and localization of UNC93B1 and TLR9. In contrast, CpG DNA-stimulated TLR9 signaling was severely inhibited in cells expressing UNC93B1(N272Q), but not in cells with UNC93B1(N251Q). Further, it was found that glycosylation at Asn272 of UNC93B1 is essential for the recruitment of MyD88 to TLR9 and the subsequent downstream signaling. On the other hand, the defective glycosylation at Asn272 did not affect TLR7 signaling. Collectively, these data demonstrate that the glycosylation at a specific asparagine residue of UNC93B1 is required for TLR9 signaling and the glycosylation status of UNC93B1 differently affects activation of TLR7 and TLR9.
Toll 样受体 (TLRs) 通过识别病原体相关分子模式并启动先天免疫反应,在宿主防御病原体的第一线中发挥关键作用。TLRs 在特定亚细胞隔室中的正确定位对于其配体识别和下游信号传导至关重要,以确保针对病原体的适当反应,同时避免错误或过度激活。几种 TLR,包括 TLR7 和 TLR9,但不包括 TLR4,依赖 UNC93B1 进行其适当的细胞内定位和信号传导。越来越多的证据表明,UNC93B1 差异调节其各种客户 TLR,但 UNC93B1 控制个体 TLR 的具体机制尚不清楚。蛋白 N-糖基化是发生在膜定位或分泌蛋白中的最常见和最重要的翻译后修饰之一。UNC93B1 先前被证明在 Asn251 和 Asn272 残基上发生糖基化。在这项研究中,我们通过比较野生型和糖基化缺陷突变 UNC93B1 蛋白,研究了 UNC93B1 的 N-糖基化是否通过影响其功能。结果发现,Asn251 和 Asn272 残基的糖基化可以相互独立发生,UNC93B1 中的 N251Q 或 N272Q 突变均不改变 UNC93B1 和 TLR9 的表达和定位。相比之下,CpG DNA 刺激的 TLR9 信号在表达 UNC93B1(N272Q)的细胞中受到严重抑制,但在具有 UNC93B1(N251Q)的细胞中不受抑制。此外,研究发现 UNC93B1 上 Asn272 的糖基化对于 MyD88 招募到 TLR9 以及随后的下游信号传导至关重要。另一方面,Asn272 处的糖基化缺陷突变不影响 TLR7 信号。总之,这些数据表明 UNC93B1 上特定天冬酰胺残基的糖基化对于 TLR9 信号至关重要,并且 UNC93B1 的糖基化状态对 TLR7 和 TLR9 的激活有不同的影响。