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Series GSE35601 Query DataSets for GSE35601
Status Public on Dec 01, 2012
Title Influence of Interferon-beta on expression profile of memory T-cells
Organism Homo sapiens
Experiment type Expression profiling by array
Summary Inflammasomes are multi-protein complexes that control the production of pro-inflammatory cytokines such as IL-1beta. Inflammasomes play an important role in the control of immunity to tumors and infections, and also in autoimmune diseases, but the mechanisms controlling the activation of human inflammasomes are largely unknown. We found that human activated CD4+CD45RO+ memory T-cells specifically suppress P2X7R-mediated NLRP3 inflammasome activation, without affecting P2X7R-independent NLRP3 or NLRP1 inflammasome activation. The concomitant increase in pro-IL-1β production induced by activated memory T-cells concealed this effect. Priming with IFNβ decreased pro-IL-1β production in addition to NLRP3 inflammasome inhibition and thus unmasked the inhibitory effect on NLRP3 inflammasome activation. IFNβ did not suppress NLRP3 inflammasome activation by acting directly on monocytes. The inhibition of pro-IL-1β production and suppression of NLRP3 inflammasome activation by IFNβ-primed human CD4+CD45RO+ memory T-cells is partly mediated by soluble FasL and is associated with down-regulated P2X7R mRNA expression and reduced response to ATP in monocytes. CD4+CD45RO+ memory T-cells from multiple sclerosis (MS) patients showed a reduced ability to suppress NLRP3 inflammasome activation, however their suppressive ability was recovered following in vivo treatment with IFNβ. Thus, our data demonstrate that human P2X7R-mediated NLRP3 inflammasome activation is regulated by activated CD4+CD45RO+ memory T cells, and provide new information on the mechanisms mediating the therapeutic effects of IFNβ in MS.
 
Overall design Memory T-cells were cultured in the presence of monocytes with and without Interferon-beta, resorted and expression profile was determined
 
Contributor(s) Beynon V, Quintana FJ, Weiner HL
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Submission date Feb 07, 2012
Last update date Jul 26, 2018
Contact name Vanessa Beynon
Organization name Brigham and Women's Hospital
Street address 77 Avenue Louis Pasteur
City Boston
ZIP/Postal code 02115
Country USA
 
Platforms (1)
GPL6244 [HuGene-1_0-st] Affymetrix Human Gene 1.0 ST Array [transcript (gene) version]
Samples (4)
GSM871405 Untreated 1
GSM871406 Untreated 2
GSM871407 Treated 1
Relations
BioProject PRJNA152523

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Supplementary file Size Download File type/resource
GSE35601_RAW.tar 17.9 Mb (http)(custom) TAR (of CEL)
Processed data included within Sample table

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