The Inhibitory Receptor GPR56 (Adgrg1) Is Specifically Expressed by Tissue-Resident Memory T Cells in Mice But Dispensable for Their Differentiation and Function In Vivo

Tissue-resident memory T (T-RM) cells with potent antiviral and antibacterial functions protect the epithelial and mucosal surfaces of our bodies against infection with pathogens. The strong proinflammatory activities of T-RM cells suggest requirement for expression of inhibitory molecules to restrain these memory T cells under steady state conditions. We previously identified the adhesion G protein-coupled receptor GPR56 as an inhibitory receptor of human cytotoxic lymphocytes that regulates their cytotoxic effector functions. Here, we explored the expression pattern, expression regulation, and function of GPR56 on pathogen-specific CD8(+) T cells using two infection models. We observed that GPR56 is expressed on T-RM cells during acute infection and is upregulated by the T-RM cell-inducing cytokine TGF-beta and the T-RM cell-associated transcription factor Hobit. However, GPR56 appeared dispensable for CD8(+) T-cell differentiation and function upon acute infection with LCMV as well as Listeria monocytogenes. Thus, T-RM cells specifically acquire the inhibitory receptor GPR56, but the impact of this receptor on T-RM cells after acute infection does not appear essential to regulate effector functions of T-RM cells.

Automated summary

An inhibitory receptor GPR56 is specifically acquired by tissue-resident memory T (T-RM) cells during acute infection, but its impact on regulating effector functions of T-RM cells seems to be dispensable. The expression of GPR56 on T-RM cells is upregulated by the cytokine TGF-beta and the transcription factor Hobit.