Contact: mpipkin@scripps.edu
Supported by NIAID #1P01AI145815-01A1: Transcription factor regulation of CD4 and CD8 T cell effector and memory differentiation and function
- CD8+ T cells play a key role in anti-viral and anti-tumor immune responses. Upon stimulation, antigen inexperienced naïve CD8+ T cells undergo rapid expansion and extensive chromatin landscape remodeling & transcriptional profile reprogramming, leading to formation of different phenotypes.
- This is a repository of ATAC-seq genome tracks of murine CD8 T cells, together with ChIP-seq tracks of important transcription factors in CD8 T cells. It can be used as a reference for CD8 T cell chromatin landscape at different stages of development / phenotypes.
- Consider citing Immunity (2018) and original references
- In vitro TCR stimulation time points:
- 0, 2, 6, 12, 24 hours
- WT and Runx3KO P14 cells
- GEO accession number: GSE111149
- In vitro cultured CD8 T cells:
- High(100U) / low(10U) IL-2 levels
- Different combinations of PMA/Iono/CsA stimulation
- GEO accession number: GSE88987
- In vivo sorted CD8 T cells phenotypes:
- Naive, MPEC, SLEC, Memory, Exhausted
- GEO accession number: GSE88987
Bach2 BATF cJun IRF4 JunB JunD Runx3 day6 (d6) Runx3 ex vivo Stat5a Stat5b Tbet Tcf7