Decreased ERK and JNK signaling contribute to gene overexpression in “senescent” CD4+CD28– T cells through epigenetic mechanisms
Open Access
- 20 October 2009
- journal article
- Published by Oxford University Press (OUP) in Journal of Leukocyte Biology
- Vol. 87 (1), 137-145
- https://doi.org/10.1189/jlb.0809562
Abstract
Decreased ERK and JNK signaling in CD4+CD28− T cells decreases DNA methyltransferase levels causes demethylation and overexpression of genes normally suppressed by chromatin structure. An inflammatory and cytotoxic CD4+CD28– T cell subset infiltrates atherosclerotic plaques and is implicated in plaque rupture and myocardial infarctions. This pathologic subset develops with replicative stress and is found in patients with chronic inflammatory diseases such as RA as well as with aging. CD4+CD28– cells overexpress genes normally suppressed by DNA methylation in CD4+CD28+ T cells, such as KIR, perforin, and CD70. How this subset overexpresses methylation-sensitive genes is unknown. DNA methylation patterns are maintained in proliferating cells by Dnmts, which are up-regulated during mitosis by the ERK and JNK signaling pathways. We hypothesized that defects in these signaling pathways contribute to altered gene expression in human CD4+CD28– cells through effects on DNA methylation. We report that signaling through the ERK and JNK pathways is decreased in CD4+CD28– relative to CD4+CD28+ cells from the same individuals and that ERK and JNK pathway inhibition decreases Dnmt1 and −3a levels, which in turn, causes demethylation and overexpression of the TNFSF7 (CD70) gene. We also report that CD4+CD28– T cells overexpress PP5, a stress-induced inhibitor of the ERK and JNK signaling pathways that may contribute to the signaling defects. We conclude that decreased ERK and JNK signaling in the CD4+CD28– subset, arising with replicative stress, can lead to the overexpression of normally suppressed genes through effects on Dnmts and consequently, chromatin structure.Keywords
Funding Information
- National Institutes of Health (AG25877, AR42525, ES015214, AG024824)
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