Cutting Edge: Chromatin Accessibility Programs CD8 T Cell Memory.
Christopher D ScharerAlexander P R BallyBhanu GandhamJeremy M BossPublished in: Journal of immunology (Baltimore, Md. : 1950) (2017)
CD8 T cell memory is characterized by rapid recall of effector function, increased proliferation, and reduced activation requirements. Despite the extensive functional characterization, the molecular mechanisms that facilitate these enhanced properties are not well characterized. In this study, the assay for transposase-accessible chromatin sequencing was employed to map the cis-regulatory elements in CD8 T cells responding to acute and chronic lymphocytic choriomeningitis virus infections. Integration of chromatin accessibility profiles with gene expression data identified unique regulatory modules that were enriched for distinct combinations of transcription factor-binding motifs. Memory CD8 T cells displayed a chromatin accessibility structure that was absent from other acute and exhausted cells types and included key effector and proliferative genes. Stimulation of memory cells revealed enhanced transcription of "memory-primed" genes compared with naive cells. Thus, memory CD8 T cells display a preprogrammed chromatin accessibility profile and maintain a molecular history of cis-element usage, thereby reducing the steps necessary to revive effector functions.
Keyphrases
- transcription factor
- gene expression
- induced apoptosis
- genome wide
- working memory
- dna damage
- cell cycle arrest
- genome wide identification
- dna binding
- regulatory t cells
- liver failure
- dna methylation
- dendritic cells
- endoplasmic reticulum stress
- oxidative stress
- single cell
- public health
- drug induced
- electronic health record
- high throughput
- hepatitis b virus
- intensive care unit
- cell proliferation
- machine learning
- immune response
- artificial intelligence
- type iii
- high density
- deep learning