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Status |
Public on Sep 21, 2017 |
Title |
The Ets-family transcription factors PU.1 and SpiB are redundantly required by mature B cells to sense and respond to environmental cues |
Organism |
Mus musculus |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
Humoral immunity requires B cells to respond to multiple stimuli, including antigen, membrane and soluble ligands and microbial products. Ets-family transcription factors regulate many aspects of hematopoiesis, although their roles in humoral immunity have proven difficult to decipher, potentially due to redundancy between the family members. Here we show that mice lacking both PU.1 and SpiB in mature B cells are unable to respond protein antigen, preventing germinal center formation and high-affinity antibody production. Mutant B cells also showed impaired survival following engagement of the CD40 and TLR pathways, but paradoxically enhanced plasma cell differentiation. PU.1 and SpiB control the expression of many components of the BCR signaling pathway and the receptors for CD40L, BAFF and toll ligands. Thus PU.1 and SpiB function enables B cells to appropriately respond to environmental cues.
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Overall design |
Transcriptional profiling of PU.1-/- and SpiB-/- activated B cells using RNA sequencing
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Contributor(s) |
Willis SN, Liao Y, Shi W, Nutt SL |
Citation(s) |
29127283 |
Submission date |
Nov 21, 2016 |
Last update date |
Jul 25, 2021 |
Contact name |
Wei Shi |
E-mail(s) |
Wei.Shi@onjcri.org.au
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Organization name |
Olivia Newton John Cancer Research Institute
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Department |
Bioinformatics and Cancer Genomics
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Street address |
Level 5, ONJ Cancer Centre, 145 Studley Rd
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City |
Heidelberg |
State/province |
VIC |
ZIP/Postal code |
3084 |
Country |
Australia |
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Platforms (1) |
GPL19057 |
Illumina NextSeq 500 (Mus musculus) |
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Samples (24)
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Relations |
BioProject |
PRJNA354406 |
SRA |
SRP093748 |