Myeloid immune checkpoint ILT3/LILRB4/gp49B can co-tether fibronectin with integrin on macrophages.
So ItoiNaoyuki TakahashiHaruka SaitoYusuke MiyataMei-Tzu SuDai KezukaFumika ItagakiShota EndoHiroshi FujiiHideo HarigaeYuzuru SakamotoToshiyuki TakaiPublished in: International immunology (2022)
LILRB4 (B4, also known as ILT3/CD85k) is an immune checkpoint of myeloid lineage cells, albeit its mode of function remains obscure. Our recent identification of a common ligand for both human B4 and its murine ortholog gp49B as the fibronectin (FN) N-terminal 30 kDa domain poses the question of how B4/gp49B regulate cellular activity upon recognition of FN in the plasma and/or the extracellular matrix. Since FN in the extracellular matrix is tethered by FN-binding integrins, we hypothesized that B4/gp49B would tether FN in cooperation with integrins on the cell surface, thus they should be in close vicinity to integrins spatially. This scenario suggests a mode of function of B4/gp49B by which the FN-induced signal is regulated. The FN pull-down complex was found to contain gp49B and integrin β 1 in bone marrow-derived macrophages. The confocal fluorescent signals of the three molecules on the intrinsically FN-tethering macrophages were correlated to each other. When FN-poor macrophages adhered to culture plates, the gp49-integrin β 1 signal correlation increased at the focal adhesion, supporting the notion that gp49B and integrin β 1 become spatially closer to each other there. Adherence of RAW264.7 and THP-1 cells to immobilized FN induced phosphorylation of spleen tyrosine kinase, whose level was augmented under B4/gp49B deficiency. Thus, we concluded that B4/gp49B can co-tether FN in cooperation with integrin in the cis configuration on the same cell, forming a B4/gp49B-FN-integrin triplet as a regulatory unit of a focal adhesion-dependent pro-inflammatory signal in macrophages.
Keyphrases
- extracellular matrix
- tyrosine kinase
- induced apoptosis
- dendritic cells
- endothelial cells
- transcription factor
- high glucose
- adipose tissue
- single cell
- cystic fibrosis
- cell therapy
- stem cells
- cell cycle arrest
- cell proliferation
- endoplasmic reticulum stress
- biofilm formation
- mass spectrometry
- staphylococcus aureus
- heat shock protein
- cell death
- type iii