Department of Chemistry, Indiana University, Bloomington, Indiana 47405, United States.
J Phys Chem B. 2022 Aug 11;126(31):5781-5792. doi: 10.1021/acs.jpcb.2c03557. Epub 2022 Aug 1.
Innate immune cells recognize and elicit responses against pathogens by integrating signals from different types of cell-surface receptors. How the receptors interact in the membrane to enable their signaling crosstalk is poorly understood. Here, we reveal the nanoscale organization of TLR2 and Dectin-1, a receptor pair known to cooperate in regulating antifungal immunity, through their synergistic signaling crosstalk at macrophage cell membranes. Using super-resolution single-molecule localization microscopy, we show that discrete noncolocalized nanoclusters of Dectin-1 and TLR2 are partially overlapped during their synergistic crosstalk. Compared to when one type of receptor is activated alone, the simultaneous activation of Dectin-1 and TLR2 leads to a higher percentage of both receptors being activated by their specific ligands and consequently an increased level of tyrosine phosphorylation. Our results depict, in nanoscale detail, how Dectin-1 and TLR2 achieve synergistic signaling through the spatial organization of their receptor nanoclusters.
先天免疫细胞通过整合来自不同类型细胞表面受体的信号来识别和引发对病原体的反应。受体如何在膜中相互作用以实现信号串扰尚不清楚。在这里,我们通过巨噬细胞膜上的协同信号串扰揭示了 TLR2 和 Dectin-1(一对已知在调节抗真菌免疫中合作的受体)的纳米级组织。使用超分辨率单分子定位显微镜,我们表明,在协同串扰过程中,Dectin-1 和 TLR2 的离散非共定位纳米簇部分重叠。与单独激活一种受体相比,同时激活 Dectin-1 和 TLR2 导致其特定配体激活的两种受体的比例更高,并且酪氨酸磷酸化水平增加。我们的结果以纳米级细节描绘了 Dectin-1 和 TLR2 如何通过其受体纳米簇的空间组织实现协同信号传递。