MyD88 is an essential regulator of NK cell-mediated clearance of MCMV infection

The signaling adapter MyD88 is critical for immune cell activation in response to viral or bacterial pathogens via several TLRs, IL-1 beta R and IL-18R. However, the essential role of MyD88 during activations mediated by germlineencoded NK cell receptors (NKRs), such as Ly49H or NKG2D, has yet to be investigated. To define the NK cellintrinsic function of MyD88, we generated a novel NK cell conditional knockout mouse for MyD88 (Myd88fl/ flNcr1Cre/+). Phenotypic characterization of these mice demonstrated that MyD88 is dispensable for NK cell development and maturation. However, the MyD88-deficient NK cells exhibited significantly reduced cytotoxic potentials in vivo. In addition, the lack of MyD88 significantly reduced the NKG2D-mediated inflammatory cytokine production in vitro. Consistent with this, mice lacking MyD88 were unable to respond and clear MCMV infection. Transcriptomic analyses of splenic NK cells following MCMV infection revealed that inflammatory gene signatures were upregulated in Ly49H+. In contrast, Ly49H- NK cells have significant enrichment in G2M checkpoint genes, revealing distinct transcriptomic profiles of these subsets. Our results identify a central role for MyD88 in Ly49H-dependent gene signatures, including alterations in genes regulating proliferation in Ly49H+ NK cells. In summary, our study reveals a previously unknown function of MyD88 in Ly49H-dependent signaling and in vivo functions of NK cells.

Automated summary

The signaling adapter MyD88 is critical for immune cell activation in response to viral or bacterial pathogens, but its role in NK cell development seems to be dispensable. However, MyD88 significantly affects the cytotoxic function and inflammatory cytokine production of NK cells, particularly in the context of Ly49H-dependent gene signatures.