Immunobiology Laboratory, Centro Nacional de Investigaciones Cardiovasculares Carlos III (CNIC), Madrid, Spain.
Department of Immunology, School of Medicine, Universidad Complutense de Madrid, 12 de Octubre Health Research Institute (imas12), Madrid, Spain.
Front Immunol. 2018 Apr 26;9:804. doi: 10.3389/fimmu.2018.00804. eCollection 2018.
Myeloid C-type lectin receptors (CLRs) are important sensors of self and non-self that work in concert with other pattern recognition receptors (PRRs). CLRs have been previously classified based on their signaling motifs as activating or inhibitory receptors. However, specific features of the ligand binding process may result in distinct signaling through a single motif, resulting in the triggering of non-canonical pathways. In addition, CLR ligands are frequently exposed in complex structures that simultaneously bind different CLRs and other PRRs, which lead to integration of heterologous signaling among diverse receptors. Herein, we will review how sensing by myeloid CLRs and crosstalk with heterologous receptors is modulated by many factors affecting their signaling and resulting in differential outcomes for immunity and inflammation. Finding common features among those flexible responses initiated by diverse CLR-ligand partners will help to harness CLR function in immunity and inflammation.
髓系 C 型凝集素受体 (CLRs) 是识别自我和非我的重要传感器,与其他模式识别受体 (PRRs) 协同工作。CLRs 之前根据其信号基序进行分类,分为激活或抑制受体。然而,配体结合过程的特定特征可能导致单个基序产生不同的信号,从而触发非典型途径。此外,CLR 配体经常以复杂的结构暴露,这些结构同时结合不同的 CLR 和其他 PRRs,从而导致不同受体之间的异源信号整合。在此,我们将回顾髓系 CLR 的感应以及与异源受体的串扰如何受许多因素调节,这些因素影响其信号转导,从而导致免疫和炎症的不同结果。发现不同 CLR-配体伙伴启动的这些灵活反应之间的共同特征将有助于利用 CLR 在免疫和炎症中的功能。