Abstract
Evidence including genome-wide analyses have uncovered that epigenetic mechanisms regulate differentiation and effector functions in CD8 T cells. Gene expression profiles change when CD8 T cells differentiate from naaïve T cells to memory T cells. It has been shown that this programmed differentiation is regulated by epigenetic mechanisms. Upon antigen stimulation, CD8 T cells activate and acquire effector functions to target cells. Effector molecule gene expres- sions are upregulated by epigenetic mechanisms in CD8 T cells. It is suggested that memory T cells respond more rapidly to antigens because chromatin structures of effector molecule genes are open and their gene transcriptions are poised for activation. © 2011 The Japan Society for Clinical Immunology.
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Araki, Y. (2011). The role of histone modifications in differentiation and effector function of CD8 T cells: Update review including genome-wide analysis. Japanese Journal of Clinical Immunology, 34(3), 131–137. https://doi.org/10.2177/jsci.34.131
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