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Status |
Public on Feb 10, 2017 |
Title |
Elucidation of roles of Nr4a nuclear orphan receptors and Foxp3 in thymic Treg cell development |
Organism |
Mus musculus |
Experiment type |
Expression profiling by array
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Summary |
Both Nr4a family nuclear orphan receptors and Foxp3 had been revealed to be crucial transcription factors in Treg cell development. In this study, to reveal their roles in a Treg cell developmental transcriptional programs, we compared transcriptomes among wild-type conventional CD4 T (Tconv) cells, wild-type Treg cells, Nr4a-triple-knockout (Nr4a-TKO) Treg precursor (preTreg) cells, and Foxp3-KO preTreg cells by microarray.
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Overall design |
Total RNA was extracted from wild-type Tconv (CD4-single positive (CD4SP),CD25-low) thymocytes, wild-type thymic Treg (CD4SP, Foxp3+), Nr4a-TKO preTreg (CD4SP, CD25-high, GITR-high, Nr4a3-high), and Foxp3-KO preTreg (CD4SP, CD25high, Foxp3-reporter+) cells. Each cell population was analyzed with two biological replicates.
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Contributor(s) |
Sekiya T, Yoshimura A |
Citation missing |
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Submission date |
Feb 09, 2017 |
Last update date |
Feb 02, 2018 |
Contact name |
Takashi Sekiya |
E-mail(s) |
lb-sekiya@hospk.ncgm.go.jp
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Organization name |
National Center for Global Health and Medicine
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Street address |
1-7-1 Kohnodai
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City |
Ichikawa |
State/province |
Chiba |
ZIP/Postal code |
272-0827 |
Country |
Japan |
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Platforms (1) |
GPL10787 |
Agilent-028005 SurePrint G3 Mouse GE 8x60K Microarray (Probe Name version) |
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Samples (8)
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Relations |
BioProject |
PRJNA373860 |