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Status |
Public on Jul 23, 2019 |
Title |
Study of the role of IL-12p40-related cytokines in colitis of NEMOIEC-KO mice |
Organism |
Mus musculus |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
Disruption of the epithelial barrier is considered a potential cause of inflammatory bowel disease (IBD). In this study, we employed the NEMOIEC-KO mouse model to study the immune mechanisms triggering chronic colitis downstream of an epithelial barrier defect. Colitis in NEMOIEC-KO mice is driven by commensal bacteria sensing through MyD88 signaling. The IL-12p40-related cytokines are induced upon microbial sensing and are known to act critically in promoting intestinal inflammation. Yet, the relative contribution of IL-12 versus IL-23 in eliciting intestinal pathology has been controversial. Using IL-12p40, IL-12p35 and IL-23p19 knockout mice we assessed the functional contribution of IL-12 and IL-23 to intestinal inflammation in the NEMOIEC-KO model.
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Overall design |
To investigate how p40, p35 or p19 deficiencies affect the inflammatory response in the colon of NEMOIEC-KO mice, we conducted RNA-seq-based transcriptome profiling in the colons of 6-week-old NEMOIEC-KO Il12b-/-, NEMOIEC-KO Il12a-/-, NEMOIEC-KO Il23a-/-, NEMOIEC-KO and Nemofl/fl mice. Five mice per genotype were used as biological replicates.
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Contributor(s) |
Eftychi C, Wagle P, Pasparakis M |
Citation(s) |
31350179 |
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Submission date |
Dec 04, 2018 |
Last update date |
Aug 19, 2019 |
Contact name |
Manolis Pasparakis |
E-mail(s) |
pasparakis@uni-koeln.de
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Organization name |
University of Cologne
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Department |
Institute for Genetics
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Lab |
Pasparakis Lab
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Street address |
Joseph Stelzmann Strasse, 26
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City |
Cologne |
State/province |
NRW |
ZIP/Postal code |
50931 |
Country |
Germany |
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Platforms (1) |
GPL21103 |
Illumina HiSeq 4000 (Mus musculus) |
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Samples (25)
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Relations |
BioProject |
PRJNA508301 |
SRA |
SRP172453 |