The characteristics of genome-wide DNA methylation in naïve CD4+ T cells of patients with psoriasis or atopic dermatitis

• Published in: Biochemical and biophysical research communications 2012-05, Vol.422 (1), p.157-163
• Main Authors: Han, Jihye, Park, Sin-Gi, Bae, Jae-Bum, Choi, JungKyoon, Lyu, Jae-Myun, Park, Sung Hee, Kim, Hei Sung, Kim, Young-Joon, Kim, Sangsoo, Kim, Tae-Yoon
• Format: Article
• Language: English
• Subjects: Atopic dermatitis; CD4 antigen; CD4-Positive T-Lymphocytes - immunology; Chromosomes, Human, X - genetics; Dermatitis, Atopic - genetics; Development; DNA Methylation; Epigenesis, Genetic; epigenetics; Gene regulation; Genome, Human; Genomes; Histones; Humans; Immunity - genetics; Lymphocytes T; Naïve CD4+ T cells; Polarization; Promoter Regions, Genetic; Promoters; Psoriasis; Psoriasis - genetics; Skin diseases; Transcription; Transcription factors; X chromosome
• ISSN: 0006-291X; 1090-2104
• DOI: 10.1016/j.bbrc.2012.04.128

► Some pericentomeric regions were markedly hypomethylated in psoriasis. ► The 121 genes’s promoter on chromosome X had elevated methylation in psoriasis. ► The X chromosome immune-related genes had higher hypermethylation than other genes. ► Methylation changes in naïve CD4+ T cells may affect the pathogenesis of psoriasis. Psoriasis and atopic dermatitis (AD) are skin diseases that are characterized by polarized CD4+ T cell responses. During the polarization of naïve CD4+ T cells, DNA methylation plays an important role in the regulation of gene transcription. In this study, we profiled the genome-wide DNA methylation status of naïve CD4+ T cells in patients with psoriasis or AD and healthy controls using a ChIP-seq method. Only psoriasis patient T cells, not those of AD patients, showed distinct hypomethylation (>4-fold) compared to healthy control T cells in twenty-six regions of the genome ranging in size from 10 to 70kb. These regions were mostly pericentromeric on 10 different chromosomes and incidentally coincided with various strong epigenomic signals, such as histone modifications and transcription factor binding sites, that had been observed in the ENCODE project implying the potential epigenetic regulation in psoriasis development. The gene-centric analysis indicated that the promoter regions of 121 genes on the X chromosome had dramatically elevated methylation levels in psoriasis patient T-cells compared to those from healthy controls (>4-fold). Moreover, immune-related genes on the X chromosome had higher hypermethylation than other genes (P=0.046). No such patterns were observed with AD patient T cells. These findings imply that methylation changes in naïve CD4+ T cells may affect CD4+ T cell polarization, especially in the pathogenesis of psoriasis.