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Series GSE153926 Query DataSets for GSE153926
Status Public on Jul 08, 2020
Title Gene expression profiles of wild type and Nr4a-triple knockout (Nr4a-TKO) Tnaive and iTreg 3 h
Organism Mus musculus
Experiment type Expression profiling by array
Summary In this study, we investigated the roles of Nr4a family transcription factors in Th and Treg cell differentiation from Tnaive cells. Nr4a factors were found to promote Treg cell differentiation and repress Th1 and Th2 differentiation. During Treg cell differentiation, all Nr4a factors are transiently induced in Tnaive cells immediately after TCR stimulation, whereby they mediate epigenetic changes directly or by cooperating with other transcription factors. To reveal Nr4a factors' mediated transcrptional events, we analyzed gene expression of wild type and Nr4a-tripple knockout (Nr4a-TKO) Tnaive and iTreg cells by microarray analysis.
 
Overall design Wild type and Nr4a-TKO Tnaive cells and iTreg cells at 3 h of differentiation were analyzed.
 
Contributor(s) Sekiya T, Kagawa S, Masaki K, Fukunaga K, Yoshimura A, Takaki S
Citation(s) 33665581
Submission date Jul 07, 2020
Last update date Mar 11, 2021
Contact name Takashi Sekiya
E-mail(s) lb-sekiya@hospk.ncgm.go.jp
Organization name National Center for Global Health and Medicine
Street address 1-7-1 Kohnodai
City Ichikawa
State/province Chiba
ZIP/Postal code 272-0827
Country Japan
 
Platforms (1)
GPL21163 Agilent-074809 SurePrint G3 Mouse GE v2 8x60K Microarray [Probe Name version]
Samples (4)
GSM4658487 WT Tnaive
GSM4658488 Nr4a-TKO Taive
GSM4658489 WT iTreg 3 h
This SubSeries is part of SuperSeries:
GSE153928 Roles of Nr4a family transcription factors in Th and Treg cell differentiation from Tnaive cells
Relations
BioProject PRJNA644558

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

Supplementary file Size Download File type/resource
GSE153926_RAW.tar 60.9 Mb (http)(custom) TAR (of TXT)
Processed data included within Sample table

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