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Series GSE19174 Query DataSets for GSE19174
Status Public on May 01, 2010
Title PARP1 and Salmonella
Organism Mus musculus
Experiment type Expression profiling by array
Summary BACKGROUND & AIMS: The immune system comprises an innate and an adaptive immune response to combat pathogenic agents. The human enteropathogen Salmonella enterica serovar Typhimurium invades the intestinal mucosa and triggers an early innate pro-inflammatory host gene response, which results in diarrheal disease. Several host factors are involved in the acute early response to Salmonella infection. Transcription factors and transcription co-regulators have an especially important function, because they are required for the expression and synthesis of pro-inflammatory cytokines, chemokines and adhesion molecules. A central transcription factor involved in inflammation is NF-κB, which requires the nuclear protein PARP1 as co-factor for the expression of some of its target genes. Here, we investigated the role of PARP1 during Salmonella infection using a mouse model for Salmonella-induced colitis.
METHODS: To study enterocolitis by Salmonella Typhimurium, an established mouse model system, which relies on streptomycin-pretreatment prior to Salmonella infection, was employed. Histopathologic signs of inflammation and cecum colonization at various time-points after infection of wild type and PARP1 knockout mice were analyzed. PARP1 expression in the gut mucosa was studied by quantitative RT-PCR, Western blot and immunofluorescence. Gene expression profiles of infected and control infected mice in the wild type or PARP1 knockout background were obtained by whole mouse genome arrays and confirmed by quantitative RT-PCR.
 
Overall design 2 genotypes (wildtype, PARP1 knockout), 2 treatments (Salmonella SB300 infection, Salmonella SB161 control infection), 2 time-points (6h, 10h). 2-3 replicates/condition.
 
Contributor(s) Altmeyer M, Barthel M, Eberhard M, Rehrauer H, Hardt W, Hottiger M
Citation(s) 20515923
Submission date Nov 24, 2009
Last update date May 10, 2018
Contact name Hubert Rehrauer
E-mail(s) [email protected]
Organization name ETH Zurich / University of Zurich
Department FGCZ
Street address Winterthurerstr. 190
City Zurich
ZIP/Postal code 8057
Country Switzerland
 
Platforms (1)
GPL4134 Agilent-014868 Whole Mouse Genome Microarray 4x44K G4122F (Feature Number version)
Samples (11)
GSM475303 MOH2wt Sm_infected 01
GSM475304 MOH2wt Sm_infected 02
GSM475305 MOH2wt Sm_infected 03
Relations
BioProject PRJNA120589

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

Supplementary file Size Download File type/resource
GSE19174_RAW.tar 106.8 Mb (http)(custom) TAR (of TXT)
Processed data included within Sample table

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