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Status |
Public on Apr 03, 2019 |
Title |
Cognate T cell interactions affect the DC transcriptome [dataset 4] |
Organism |
Mus musculus |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
Our data suggest that peptide-presenting DC receive signals from synapse-forming antigen specific CD4+ or CD8+ T cells that alter the DC expression profile. To further test this notion, we hock immunized T cell-engrafted mice with NP harboring CpG and coated with OVA (OVA / CpG NP) or the control antigen BSA (BSA / CpG NP) and isolated NP+ DC for RNAseq.
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Overall design |
NP+ DC were isolated 20 hrs post sub-cutaneous immunization with (OVA/CpG) NP or (BSA/CpG) NP from popliteal and inguinal lymph nodes. (OVA / CpG) or (BSA/CpG) NP+ DC were single-cell sorted into 384w-plates, barcoded and MARS-sequenced.
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Contributor(s) |
Curato C, Jaitin DA, Giladi A, David E, Leshkowitz D, Jung S |
Citation missing |
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Submission date |
Apr 02, 2019 |
Last update date |
Apr 04, 2019 |
Contact name |
Steffen Jung |
E-mail(s) |
s.jung@weizmann.ac.il
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Phone |
0097289342787
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Organization name |
The Weizmann Institute of Science
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Department |
Immunology and Regenerative Biology
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Lab |
Steffen Jung
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Street address |
Herzl
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City |
REHOVOT |
ZIP/Postal code |
76100 |
Country |
Israel |
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Platforms (1) |
GPL19057 |
Illumina NextSeq 500 (Mus musculus) |
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Samples (4)
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This SubSeries is part of SuperSeries: |
GSE129215 |
IL-23 producing IL-10Rα-deficient gut macrophages elicit an IL-22-driven pro-inflammatory epithelial cell response |
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Relations |
BioProject |
PRJNA530541 |
SRA |
SRP190166 |