Metabolomics,Unknown,Transcriptomics,Genomics,Proteomics

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Transcription profiling of mouse immature pDC and pDC activated with CpG 1826 and influenza virus PR8


ABSTRACT: CpG 1826 binds to Toll-like receptor (TLR)9, whereas influenza virus PR8 activates pDC via TLR7. Differential stimulation of pDCs is expected to result in unique activation mechanism(s) leading to a different phenotypically and functionally matured pDC; We used microarrays to detail the global programme of gene expression underlying the maturation process of pDC activated with CpG 1826 and influenza virus PR8. We identified a distinct expression profile of upregulated immunomediators. Experiment Overall Design: Sorted pDCs were cultured for 1h and 4hs in medium control or with 5 µg/ml CpG 1826 or 300 HAU/ml purified influenza A/PR/8 virus. The first experiment (e1) included pDC in media and stimulated with CpG for 4h. In two other independent experimental batches (e2 and e3), we obtained samples of sorted pDC cultured in medium alone (med), and with CpG or PR8 (flu) for 1h and 4h. RNA extraction was performed using the RNeasy Kit (Qiagen) and hybridization on Affymetrix microarrays was performed using standard protocols. We sought to obtain homogeneous populations of pDCs at different time points under defined activation conditions in order to decipher the temporal resolution of expression profiles during the process of their maturation.

ORGANISM(S): Mus musculus

SUBMITTER: Amaya Iparraguirre 

PROVIDER: E-GEOD-7831 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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Publications

Two distinct activation states of plasmacytoid dendritic cells induced by influenza virus and CpG 1826 oligonucleotide.

Iparraguirre Amaya A   Tobias John W JW   Hensley Scott E SE   Masek Katherine S KS   Cavanagh Lois L LL   Rendl Michael M   Hunter Christopher A CA   Ertl Hildegund C HC   von Andrian Ulrich H UH   Weninger Wolfgang W  

Journal of leukocyte biology 20071120 3


There is growing evidence that plasmacytoid dendritic cells (pDC) are involved in the innate recognition of various microbes. However, the precise consequences of pathogen recognition on pDC activation and function are incompletely understood. Using a novel transgenic mouse model that facilitates the isolation of highly pure pDC populations, we found that influenza virus PR/8, a TLR7 ligand, and CpG 1826 oligonucleotide, a TLR9 ligand, induced surprisingly divergent activation programs in these  ...[more]

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