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Status |
Public on Jul 30, 2020 |
Title |
RNA-seq in mouse CD8+ T cells cultured with medium with or without methionine |
Organism |
Mus musculus |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
Abnormal epigenetic patterns correlate with effector T cell malfunction in tumors. However, their causal link is unknown. Here, we show that tumor cells disrupt methionine metabolism in CD8+ T cells, thereby lowering intracellular methionine levels and the methyl donor S-adenosylmethionine (SAM), resulting in loss of H3K79me2. Consequently, loss of H3K79me2 impaired T cell immunity. Our work reveals a novel mechanistic connection between methionine metabolism, histone patterns, and T cell immunity in the tumor microenvironment.
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Overall design |
CD8+ T cells were cultured with fresh medium without methionine (fresh-), fresh medium with methionine (fresh+), B16F10 supernatants (Sup-), and B16F10 supernatants with methionine supplementation (Sup+) for 36h, quadruplicate per group.
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Contributor(s) |
Bian Y, Li W, Zou W |
Citation(s) |
32879489 |
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Submission date |
May 19, 2020 |
Last update date |
Sep 10, 2020 |
Contact name |
Yingjie Bian |
E-mail(s) |
yingjieb@umich.edu
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Organization name |
University of Michigan
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Department |
Surgery
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Street address |
109 Zina Pitcher Pl
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City |
Ann Arbor |
State/province |
MI |
ZIP/Postal code |
48109 |
Country |
USA |
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Platforms (1) |
GPL21103 |
Illumina HiSeq 4000 (Mus musculus) |
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Samples (16)
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This SubSeries is part of SuperSeries: |
GSE150887 |
Cancer SLC43A2 alters T cell methionine metabolism and histone methylation |
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Relations |
BioProject |
PRJNA633916 |
SRA |
SRP262370 |