| First Author | Naito T | Year | 2018 |
| Journal | Mol Immunol | Volume | 94 |
| Pages | 140-152 | PubMed ID | 29310022 |
| Mgi Jnum | J:318489 | Mgi Id | MGI:6859860 |
| Doi | 10.1016/j.molimm.2017.12.021 | Citation | Naito T, et al. (2018) Loss of Eed leads to lineage instability and increased CD8 expression of mouse CD4(+) T cells upon TGFbeta signaling. Mol Immunol 94:140-152 |
| abstractText | Tri-methylation of lysine 27 on histone H3 (H3K27me3) is a repressive epigenetic modification catalyzed by polycomb repressive complex 2 (PRC2) that is required for proper cell fate determination as well as cellular function. Numerous studies have been performed to elucidate the role of PRC2 in T-cell differentiation and function; however, its role in the regulation of T-helper (Th) subset differentiation and identity has not been fully explored. Here, we report that Eed, an essential subunit of PRC2, is crucial to maintain the identity of CD4(+) T cells under TGFbeta-induced regulatory T cell (Treg)-polarizing conditions. Mouse CD4(+) T cells lacking Eed exhibited unstable CD4 expression upon TCR stimulation in vitro. Helper lineage instability was further augmented by Treg-polarizing conditions, leading to the immense up-regulation of CD8alpha as well as other molecules, resembling CD4(+) CD8alphaalpha(+) intraepithelial lymphocyte (DP-IEL) differentiation. Genetic studies suggested that the altered balance between transcription factors T-bet, Runx3, and Th-POK underlies the induction of the DP-IEL-like phenotype in Eed-deficient CD4(+) cells. Furthermore, comparison to Th1- and Th17-polarizing conditions indicated that cooperation between Smad3 and the T-bet-Runx3 axis facilitated by the loss of H3K27me3 is crucial for phenotype induction. Collectively, our results provide insight into the molecular mechanism that maintains and regulates the proper cellular response upon TGFbeta signaling in CD4(+) T cells. |
