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Status |
Public on Mar 29, 2018 |
Title |
Development of plasma cell-prone germinal center B cells |
Organism |
Mus musculus |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
Higher- or lower-affinity GC B cells are directed to plasma cell or recycling GC cell fates; however, how commitment to the plasma cell fate takes place is unclear. By using the level of Bcl6 as a marker, we found that a population of light zone (LZ) GC cells, Bcl6loCD69hi with IRF4 and higher-affinity BCRs or Bcl6hiCD69hi with lower- affinity BCRs, favored the plasma cell or recycling GC cell fate, respectively. Mechanistically, CD40 acted as a dose-dependent regulator for Bcl6loCD69hi cell formation. Furthermore, we found that ICAM1 and SLAM levels on Bcl6loCD69hi cells were higher than on Bcl6hiCD69hi cells, thereby affording more stable TFH-GC B cell contacts, while attenuating this contact down-regulated IRF4. These data support the model that commitment to the plasma cell begins in the GC, and suggest that stability and possibly duration of TFH-GC B cell contacts are key for formation of plasma cell-prone precursor GC cells.
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Overall design |
mRNA profiles of GC B cell subsets and GC-derived plasmablast were generated by barcode-based digital RNA sequencing.
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Contributor(s) |
Ise W, Shiroguchi K, Kurosaki T |
Citation(s) |
29669250 |
Submission date |
Jan 26, 2018 |
Last update date |
Jan 27, 2019 |
Contact name |
Eri Nishiyama |
E-mail(s) |
eri.nishiyama@riken.jp
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Organization name |
Riken
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Department |
Center for Biosystems Dynamics Research
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Lab |
Laboratory for Prediction of Cell Systems Dynamics
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Street address |
6-2-3 Furuedai
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City |
Suita |
State/province |
Osaka |
ZIP/Postal code |
565-0874 |
Country |
Japan |
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Platforms (1) |
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Samples (15)
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Relations |
BioProject |
PRJNA431808 |
SRA |
SRP131526 |