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Status |
Public on Apr 30, 2019 |
Title |
Chromatin immunoprecipitation sequencing (ChIP-Seq) for Bhlhe40 from naïve and IL-4c-stimulated large peritoneal macrophages (LPMs) |
Organism |
Mus musculus |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
Most tissue-resident macrophage populations develop during embryogenesis, self-renew in the steady state, and can expand during type 2 immunity. Whether shared mechanisms regulate macrophage proliferation in homeostasis and disease is unclear. We found that the transcription factor Bhlhe40 was cell-intrinsically required in large peritoneal macrophages (LPMs) for self-renewal and maintenance, but was not required in other resident macrophages. Bhlhe40 was selectively necessary in LPMs for proliferation, but not polarization, in response to IL-4. During a helminth infection, Bhlhe40 was required for normal LPM cell cycling. Bhlhe40 repressed the expression of Maf and Mafb and directly promoted expression of cell cycle-related transcripts to enable proliferation of LPMs. Genomic sites bound by Bhlhe40 in LPMs included some co-bound by the macrophage lineage-determining factor PU.1 and others uniquely bound by Bhlhe40, including Maf and cell cycle-related loci. Our findings demonstrate a tissue-specific control mechanism regulating resident macrophage proliferation in homeostasis and type 2 immunity.
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Overall design |
LPMs were sorted from pooled naïve and pooled IL-4c-treated C57BL/6 mice. Chromatin was crosslinked and immunoprecipitation (Novus Biologicals, anti-Dec1, catalog NB100-1800, Lot C1) was performed for Bhlhe40-bound genomic regions, which were sequenced along with input DNA controls from the same samples. DNA from 1 naïve LPM ChIP and 1 IL-4c-stimulated ChIP were sequenced, as well as input DNA. Cells were pooled from multiple mice for each immunoprecipitation.
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Contributor(s) |
Jarjour NN, Shchukina I, Edelson BT |
Citation(s) |
31061528 |
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Submission date |
Jan 28, 2019 |
Last update date |
Jul 30, 2019 |
Contact name |
Brian T Edelson |
E-mail(s) |
bedelson@path.wustl.edu
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Organization name |
Washington University in St. Louis
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Department |
Pathology and Immunology
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Lab |
Rm. 8304
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Street address |
425 S. Euclid Ave.
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City |
St. Louis |
State/province |
MO |
ZIP/Postal code |
63110 |
Country |
USA |
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Platforms (1) |
GPL21493 |
Illumina HiSeq 3000 (Mus musculus) |
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Samples (4)
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This SubSeries is part of SuperSeries: |
GSE125730 |
Bhlhe40 mediates tissue-specific control of macrophage proliferation in homeostasis and type 2 immunity |
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Relations |
BioProject |
PRJNA517407 |
SRA |
SRP182643 |