PD-L1 regulates inflammatory macrophage development from human pluripotent stem cells by maintaining interferon-gamma signal

Abstract

AbstractPD-L1 (programmed death-ligand 1) serves as a pivotal immune checkpoint in both the innate and adaptive immune systems. PD-L1 is expressed in macrophages in response to interferon-gamma (IFNγ). We examined whether PD-L1 might regulate macrophage development. We establishedPD-L1-/-human pluripotent stem cells, differentiated them into macrophages, and observed a 60% reduction of CD11B+CD45+macrophages inPD-L1-/-, orthogonally verified with PD-L1 inhibitor BMS-1166 reduced macrophages to the same fold. Single-cell RNA sequencing further confirmed the 60% reduction of macrophages as well as the down-regulation of macrophage-defining transcription factorsSPI1, KLF6, andMAFB. Further,PD-L1-/-macrophages reduced the level of inflammatory signals such as NFκB, TNF, and chemokines CXCL and CCL families. Whilst anti-inflammatory TGF-β was upregulated. Finally, we identified thatPD-L1-/-macrophages significantly down-regulated interferon-stimulated genes (ISGs) despite IFNγ in differentiation media. Mechanistically,PD-L1-/-macrophages reducedIFNGR1expression explaining that cells could not respond to IFNγ. These data suggest that PD-L1 regulates inflammatory macrophage development by maintaining the IFNγ signal.