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| Status |
Public on Jun 20, 2014 |
| Title |
Transcriptome and Molecular Pathways Analysis of CD4 T-Cells from Young NOD Mice |
| Organism |
Mus musculus |
| Experiment type |
Expression profiling by array
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| Summary |
Type 1 diabetes is a multigenic disease caused by T-cell mediated destruction of the insulin producing β-cells. Although conventional (targeted) approaches of identifying causative genes have advanced our knowledge of this disease, many questions remain unanswered. Using a whole molecular systems study, we unraveled the genes/molecular pathways that are altered in CD4 T-cells from young NOD mice prior to insulitis (lymphocytic infiltration into the pancreas). Many of the CD4 T-cell altered genes lie within known diabetes susceptibility regions (Idd), including several genes in the diabetes resistance region Idd13 and two genes (Khdrbs1 and Ptp4a2) in the CD4 T-cell diabetogenic activity region Idd9/11. Alterations involved apoptosis/cell proliferation and metabolic pathways (predominant at 2 weeks), inflammation and cell signaling/activation (predominant at 3 weeks), and innate and adaptive immune responses (predominant at 4 weeks). We identified several factors that may regulate these abnormalities: IRF-1, HNF4A, TP53, BCL2L1 (lies within Idd13), IFNG, IL4, IL15, and prostaglandin E2, which were common to all 3 ages; AR and IL6 to 2 and 4 weeks; and Interferon (IFN-I) and IRF-7 to 3 and 4 weeks. Others were unique to the various ages (e. g. MYC, JUN, and APP to 2 weeks; TNF, TGFB1, NFKB, ERK, and p38MAPK to 3 weeks; and IL12 and STAT4 to 4 weeks). Our data suggest that diabetes resistance genes in Idd13 and Idd9/11, and BCL2L1, IL6-AR and IFNG-IRF-1-IFN-I/IRF-7-IL12 pathways play an important role in CD4 T-cells in the early pathogenesis of autoimmune diabetes. Thus, the alternative approach of investigation at the molecular systems level has captured new information, which combined with validation studies, offers the opportunity to test hypotheses on the role played by the genes/molecular pathways identified in this study, to understand better the mechanisms of autoimmune diabetes in CD4 T-cells, and to develop new therapeutic strategies for the disease.
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| Overall design |
CD4 T-cells were purified from spleen leukocytes collected from 2-, 3- and 4-week old NOD mice and two age-matched control strains, NOR, and C57BL/6, (n=5 for each strain and each age group; except NOD2wk). NOR is an insulitis- and diabetes-free control strain that shares shares ~88% of its genome with NOD mice, including the diabetogenic H2g7 MHC haplotype and several important non-MHC T1D susceptibility loci. C57BL/6 is also a diabetes-resitant strain, but it is more genetically distantly related to NOD.
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| Contributor(s) |
Kakoola DN, Curcio-Brint A, Lenchik NI, Gerling IC |
| Citation(s) |
24918037 |
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| Submission date |
May 02, 2013 |
| Last update date |
Feb 11, 2019 |
| Contact name |
Dorothy N. Kakoola |
| E-mail(s) |
dkakoola@uthsc.edu
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| Organization name |
University of Tennessee Health Science Center
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| Department |
Medicine
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| Lab |
VA Research
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| Street address |
1030 Jefferson Avenue
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| City |
Memphis |
| State/province |
TN |
| ZIP/Postal code |
38104 |
| Country |
USA |
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| Platforms (1) |
| GPL1261 |
[Mouse430_2] Affymetrix Mouse Genome 430 2.0 Array |
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| Samples (44)
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| Relations |
| BioProject |
PRJNA201061 |
| Supplementary file |
Size |
Download |
File type/resource |
| GSE46600_RAW.tar |
154.2 Mb |
(http)(custom) |
TAR (of CEL) |
| Processed data included within Sample table |
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