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Home › Dataset Library › Transcription profiling of human endothelial and fibroblast cells isolated from umbilical cord veins treated with interferons to identify...

Dataset: Transcription profiling of human endothelial and fibroblast cells isolated from umbilical cord veins treated with interferons to identify genes regulated by interferons

IFNs are highly pleiotropic cytokines also endowed with marked anti-angiogenic activity. In this study, the mRNA expression profiles of...

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IFNs are highly pleiotropic cytokines also endowed with marked anti-angiogenic activity. In this study, the mRNA expression profiles of endothelial cells (EC) exposed in vitro to IFN-alpha, IFN-beta, or; IFN-gamma were determined. We found that in HUVEC as well as in other EC types 175 genes were upregulated (>2-fold increase) by IFNs, including genes involved in the host response to RNA viruses, inflammation, and apoptosis. Interestingly, 41 genes showed a >5-fold higher induction by IFN-alpha in EC compared to human fibroblasts; among them, the gene encoding the angiostatic chemokine CXCL11 was selectively induced by IFN-alpha in EC along with other genes associated; with angiogenesis regulation, including CXCL10, TRAIL, and guanylate binding protein 1 (GBP-1). These transcriptional changes were confirmed and extended by quantitative PCR analysis and ELISA; whereas IFN-alpha and IFN-beta exerted virtually identical effects on transcriptome modulation, a differential gene regulation by type I and type II IFN emerged, especially as far as quantitative aspects were concerned. In vivo, IFN-alpha-producing tumors over-expressed murine CXCL10-11,; GBP-1 and TRAIL, with evidence of CXCL11 production by tumor-associated EC. Overall, these findings improve our understanding of the anti-angiogenic effects of IFNs by showing that these cytokines trigger an anti-angiogenic transcriptional program in EC. Moreover, we suggest that quantitative differences in the magnitude of the transcriptional activation of IFNresponsive genes could form the basis for cell-specific transcriptional signatures. In press, J. Immunol. 2007. Experiment Overall Design: comparison of interferon effects on endothelial cells (HUVEC, HMVEC) and fibrobloasts

Species:
human

Samples:
23

Source:
E-GEOD-3920

PubMed:
17202376

Updated:
Dec.12, 2014

Registered:
Jun.19, 2014


Factors: (via ArrayExpress)
Sample CELLTYPE COMPOUND
GSE3920GSM89650 endothelial cell interferon gamma
GSE3920GSM89652 fibroblast interferon alpha
GSE3920GSM89642 endothelial cell control
GSE3920GSM89647 endothelial cell interferon alpha
GSE3920GSM89654 fibroblast control
GSE3920GSM89647 endothelial cell interferon alpha
GSE3920GSM89647 endothelial cell interferon alpha
GSE3920GSM89647 endothelial cell interferon alpha
GSE3920GSM89642 endothelial cell control
GSE3920GSM89654 fibroblast control
GSE3920GSM89658 fibroblast interferon gamma
GSE3920GSM89650 endothelial cell interferon gamma
GSE3920GSM89642 endothelial cell control
GSE3920GSM89641 endothelial cell interferon beta
GSE3920GSM89642 endothelial cell control
GSE3920GSM89654 fibroblast control
GSE3920GSM89658 fibroblast interferon gamma
GSE3920GSM89647 endothelial cell interferon alpha
GSE3920GSM89650 endothelial cell interferon gamma
GSE3920GSM89652 fibroblast interferon alpha
GSE3920GSM89641 endothelial cell interferon beta
GSE3920GSM89652 fibroblast interferon alpha
GSE3920GSM89642 endothelial cell control

Tags

  • cell
  • chemokine
  • protein

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