The DNA damage response pathway regulates the expression of the immune checkpoint CD47

The CD47 don't eat me marker is upregulated following exposure to DNA damaging agents, including irradiation, a process that is dependent on Mre11, a key player in the DNA damage response pathway. CD47 is a cell surface ligand expressed on all nucleated cells. It is a unique immune checkpoint protein acting as don't eat me signal to prevent phagocytosis and is constitutively overexpressed in many tumors. However, the underlying mechanism(s) for CD47 overexpression is not clear. Here, we show that irradiation (IR) as well as various other genotoxic agents induce elevated expression of CD47. This upregulation correlates with the extent of residual double-strand breaks (DSBs) as determined by gamma H2AX staining. Interestingly, cells lacking mre-11, a component of the MRE11-RAD50-NBS1 (MRN) complex that plays a central role in DSB repair, or cells treated with the mre-11 inhibitor, mirin, fail to elevate the expression of CD47 upon DNA damage. On the other hand, both p53 and NF-kappa B pathways or cell-cycle arrest do not play a role in CD47 upregualtion upon DNA damage. We further show that CD47 expression is upregulated in livers harvested from mice treated with the DNA-damage inducing agent Diethylnitrosamine (DEN) and in cisplatin-treated mesothelioma tumors. Hence, our results indicate that CD47 is upregulated following DNA damage in a mre-11-dependent manner. Chronic DNA damage response in cancer cells might contribute to constitutive elevated expression of CD47 and promote immune evasion.

Automated summary

CD47 is upregulated following DNA damage, including irradiation, which depends on the key factor Mre11 in the DNA damage response pathway. CD47 is a cell surface ligand expressed on all nucleated cells and acts as an immune checkpoint protein to prevent phagocytosis. It is constitutively overexpressed in many tumors, but the underlying mechanism(s) for CD47 overexpression is unclear.