Cutting edge: STAT activation by IL-19, IL-20 and mda-7 through IL-20 receptor complexes of two types

IL-10-related cytokines include IL-20 and IL-22, which induce, respectively , keratinocyte proliferation and acute phase production by hepatocytes, as well as IL-19, melanoma differentiation-associated gene 7, and AK155, three cytokines for which no activity nor receptor complex has been described th us far. Here, we show that mda-7 and IL-19 bind to the previously described IL-20R complex, composed by cytokine receptor family 2-8/IL-20R alpha and DIRS1/IL-20R beta (type I IL-20R). In addition, mda-7 and IL-20, but not IL -19, bind to another receptor complex, composed by IL-22R and DIRS1/ IL20R beta (type II IL-20R). In both cases, binding of the ligands results in STA T3 phosphorylation and activation of a minimal promoter including STAT-bind ing sites. Taken together, these results demonstrate that: 1) IL-20 induces STAT activation through IL-20R complexes of two types; 2) mda-7 and IL-20 redundantly signal through both complexes; and 3) IL-19 signals only throug h the type I IL-20R complex.