An epigenetic mechanism of Dll4-facilitated Foxp3+ regulatory T cells differentiation (LYM8P.637)

Abstract

Abstract Notch signaling facilitates inducible Foxp3+ regulatory T cells (iTreg) differentiation. Epigenetic modifications, which include histone modifications, are critical in cell differentiation. Recent genome-wide studies showed that iTreg have increased trimethylation on histone H3 at lysine 4 (H3K4me3) around Foxp3 loci, but the role of Notch signaling and its underlying epigenetic mechanisms remain elusive. Here we report that Delta-like ligand 4 (Dll4) but not Jagged1 can activate Notch signaling, facilitate Foxp3+ iTreg differentiation, and increased H3K4me3 around Foxp3 promoter and conserved noncoding sequences (CNS). We performed epigenetic enzyme array analysis and found one histone methyltransferase—SET and MYND domain containing protein 3 (Smyd3) that is abundant in iTreg. Dll4/Notch signaling amplified and accelerated Smyd3 expression in vitro during iTreg cell differentiation via an RBPJ-mediated transcription activation. Inhibition of Notch signaling decreased Smyd3 expression. When Smyd3 was genetically knocked out in CD4 T cells, the Dll4-enhanced H3K4me3 around the Foxp3 loci and Foxp3+ Tregs were decreased in vitro and in vivo. These results demonstrate that Notch ligand Dll4 can epigenetically regulate Foxp3+ Tregs through Smyd3.