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Series GSE185375 Query DataSets for GSE185375
Status Public on Jan 11, 2022
Title Multi-omics approaches reveal TNF-mediated inhibition of tissue reparative macrophages is via a gene-selective transcriptional mechanism (ATAC-Seq)
Organism Mus musculus
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Summary Anti-TNF therapies are a core anti-inflammatory approach for chronic diseases such as rheumatoid arthritis and Crohn’s Disease. Previously, we and others found that TNF blocks the emergence and function of alternatively-activated or M2 macrophages involved in wound healing and tissue-reparative functions. Conceivably, anti-TNF drugs could mediate their protective effects in part by an altered balanced of macrophage activity. To understand the mechanistic basis of how TNF regulates tissue-reparative macrophages we used RNAseq, scRNAseq, ATACseq, time-resolved phospho-proteomics, gene-specific approaches, metabolic analysis and signaling pathway deconvolution. Our findings reveal that TNF controls tissue-reparative macrophage gene expression in a highly gene-specific way dependent on JNK signaling. We uncover principles of the selectively inhibition by TNF via the type 1 TNF receptor on specific populations of alternative activated macrophages.
 
Overall design Chromatin accessibility profiles of wild-type BMDMs stimulated with IL4/IL13 or IL4/IL13 + TNF for 24h from 3 separate mice.
 
Contributor(s) Dichtl S, Sanin DE, Pearce EJ, Murray PJ
Citation(s) 35027468
Submission date Oct 05, 2021
Last update date Apr 19, 2022
Contact name Assa Yeroslaviz
E-mail(s) yeroslaviz@biochem.mpg.de
Organization name Max-Planck-Institute for biochemistry
Department computational Biology
Street address Am Klopferspitz 18
City Martinsried
State/province Bavaria
ZIP/Postal code 82152
Country Germany
 
Platforms (1)
GPL21493 Illumina HiSeq 3000 (Mus musculus)
Samples (9)
GSM5612151 M0_1
GSM5612152 M0_2
GSM5612153 M0_3
This SubSeries is part of SuperSeries:
GSE185380 Multi-omics approaches reveal TNF-mediated inhibition of tissue reparative macrophages is via a gene-selective transcriptional mechanism
Relations
BioProject PRJNA768838
SRA SRP340126

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE185375_RAW.tar 1.3 Gb (http)(custom) TAR (of BW)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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