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Series GSE79614 Query DataSets for GSE79614
Status Public on Mar 10, 2018
Title Nanostring of sorted lung conventional dendritic cells (cDCs) from cell-specific MyD88 KO at 6h after in vivo sensitization with OVA/standard flagellin
Organism Mus musculus
Experiment type Expression profiling by array
Summary Allergic asthma is a chronic disease of the airways characterized by eosinophilic and neutrophilic inflammation. MYD88, the adaptor molecule for TLR and IL-1 family member signaling, is required for allergic sensitization through the airway in animal models of allergic asthma. We generated conditionally mutant mice separately lacking Myd88 in airway epithelial cells (ECs) or dendritic cells (DCs) to define the contribution of Myd88 expression in each of these cell types. To examine crosstalk from ECs to conventional (c)DCs in vivo, we examined immune-specific transcriptional profiles from lung cDCs sorted following 6h in vivo lung allergic sensitization through the airways from WT MyD88 fx/fx, SPC cre+ MyD88 fx/fx (EC-MYD88 KO), CD11c cre+ MyD88 fx/fx (DC-MYD88 KO), and full MyD88 KO mice. We observed immune-specific transcriptional changes in cDCs that were cell-intrinsic as well as resulting from in vivo crosstalk from ECs. We also observed transcriptional (linked data set) and epigenetic changes in chromatin conformation in cDCs by ATAC-seq (linked data set) as well as changes in immune-specific whole lung RNA, sorted EC RNA, and sorted alveolar macrophage (AM) RNA by Nanostring nCounter Immunology Codeset Analysis (additional linked files).
 
Overall design Lung cDCs from all genotypes were flow cytometry sorted following 6h of in vivo allergic sensitization with 100 micrograms ovalbumin (OVA)/ 1250 ng standard flagellin (stFLA). Samples from all 4 genotypes (WT MyD88 fx, SPC cre+ MyD88 fx, CD11c cre+ MyD88 fx, MyD88 KO) x 1 timepoints (6 h OVA/stFLA) = 4 conditions. 4 conditions x 3-4 replicates per genotype-timepoint = 14 total samples. WT MyD88 fx/fx mice are a positive control for all genes induced following allergen sensitization, while MyD88 KO is a negative control for genes that are not induced in the full body MyD88 KO mouse. SPC cre+ MyD88 fx/fx mice test for genes that require EC-dependent MYD88 signaling, whereas CD11c cre+ MyD88 fx/fx mice test for genes that require CD11c-expressing cell-dependent MYD88 expression. Gene expression analysis was conducted using using nCounter Mouse Immunology Codeset (Nanostring, Seattle, WA) on 3-4 biological replicates for each genotype and timepoint.
 
Contributor(s) Thomas SY, Cook DN
Citation(s) 29067999
Submission date Mar 25, 2016
Last update date Jun 11, 2018
Contact name Seddon Thomas
E-mail(s) [email protected]
Organization name NIEHS
Street address 111 T. W. Alexander Dr.,
City RTP
State/province North Carolina
ZIP/Postal code 27709
Country USA
 
Platforms (1)
GPL19964 nCounter Mouse Immunology Panel
Samples (14)
GSM2099010 Lung_cDC_WT_MyD88 fx_6h_OVA_stFLA_rep1
GSM2099011 Lung_cDC_WT_MyD88 fx_6h_OVA_stFLA_rep2
GSM2099012 Lung_cDC_WT_MyD88 fx_6h_OVA_stFLA_rep3
This SubSeries is part of SuperSeries:
GSE79615 MYD88-dependent dendritic and epithelial cell crosstalk in the lung orchestrates immune responses to inhaled allergens
Relations
BioProject PRJNA316446

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
GSE79614_RAW.tar 100.0 Kb (http)(custom) TAR (of RCC)
Processed data included within Sample table

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