Spatial Organization of Dectin-1 and TLR2 during Synergistic Crosstalk Revealed by Super-resolution Imaging.
Miao LiChristopher VultoriusManisha BethiYan YuPublished in: The journal of physical chemistry. B (2022)
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.
Keyphrases
- single molecule
- toll like receptor
- immune response
- inflammatory response
- atomic force microscopy
- cancer therapy
- cell surface
- high resolution
- single cell
- sensitive detection
- stem cells
- adipose tissue
- high speed
- label free
- binding protein
- fluorescent probe
- high throughput
- photodynamic therapy
- bone marrow
- drug delivery
- antimicrobial resistance
- cell therapy
- quantum dots