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Status |
Public on Apr 30, 2020 |
Title |
Ectopic Tcf1 expression reprograms exhausted CD8+ T cells to acquire stem cell-like features [ATAC-seq] |
Organism |
Mus musculus |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
The goal of this study is to determine the capacity of Tcf1 to reprogram exhausted CD8+ T cells for function restoration. Tex cells elicited by chronic infection contain a CXCR5+Tim3– subset that has stem cell-like self-renewing capacity and expresses an elevated level of Tcf1 (termed Tex-stem), and Tex-stem cells depend on Tcf1 for generation and persistence. We show that ectopic Tcf1 expression profoundly affected the chromatin accessibility of Tex cells.
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Overall design |
Genome-wide chromatin accessibility profiles of stem cell-like exhauseted CD8+ T cells with or without ectopic Tcf1 expression.
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Contributor(s) |
Qiang S, Sheng'en H, Chongzhi Z, Hai-Hui X |
Citation(s) |
32341523 |
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Submission date |
Oct 17, 2019 |
Last update date |
Apr 30, 2020 |
Contact name |
Haihui Xue |
E-mail(s) |
haihui.xue@hmh-cdi.org
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Organization name |
Hackensack University Medial Center
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Department |
Center for Discovery and Innovation
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Lab |
Xue lab
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Street address |
123 Metro Boulevard, Bldg. 123, Rm. 5527
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City |
Nutley |
State/province |
NJ |
ZIP/Postal code |
07110 |
Country |
USA |
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Platforms (1) |
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Samples (6)
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This SubSeries is part of SuperSeries: |
GSE139058 |
Ectopic Tcf1 expression reprograms exhausted CD8+ T cells to acquire stem cell-like features |
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Relations |
BioProject |
PRJNA578114 |
SRA |
SRP226072 |