Anti-CD4 treatment-induced IL18Rαhi CD8+ T cells show highly effector profile
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ABSTRACT:
PROVIDER: PRJNA748267 | ENA |
REPOSITORIES: ENA
Dataset's files
| Action | DRS | |||
|---|---|---|---|---|
| SRR15197300_1.fastq.gz | Fastqsanger.gz | |||
| SRR15197300_2.fastq.gz | Fastqsanger.gz | |||
| SRR15197301_1.fastq.gz | Fastqsanger.gz | |||
| SRR15197301_2.fastq.gz | Fastqsanger.gz | |||
| SRR15197302_1.fastq.gz | Fastqsanger.gz |
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Project description:Differentiation of CD8+ T lymphocytes into effector and memory cells is key for an adequate immune response and relies on complex interplay of pathways that convey signals from cell surface to nucleus. In this study, we fractionated four CD8+ T cell subtypes; naïve, recently activated effector, effector and memory cells into membrane, cytosol, soluble nucleus, chromatin-bound and cytoskeleton compartments. Using LC-MS/MS analysis, identified peptides were matched to human peptides/proteins (SwissProt). Compartment fractionation and gel-LC-MS separation identified 2399 proteins in total. Among these 735 were detected in all five, 241 in four, 257 in three, 368 in two and 798 found in only one fraction. Comparison between the two most different subsets, naïve and effector, yielded 146 significantly regulated proteins.
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