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Status |
Public on Sep 15, 2006 |
Title |
Cell Specific Expression & Pathway Analyses Reveal Novel Alterations in Trauma-Related Human T-Cell & Monocyte Pathways |
Organism |
Homo sapiens |
Experiment type |
Expression profiling by array
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Summary |
Monitoring genome-wide, cell-specific responses to human disease, although challenging, holds great promise for medicine’s future. Patients with injury severe enough to develop multiple organ dysfunction syndrome (MODS) are known to have multiple immune derangements, including T-cell apoptosis and anergy combined with depressed monocyte antigen presentation. Genome-wide expression analysis of highly-enriched circulating leukocyte subpopulations, combined with cell-specific pathway analyses, offers a previously unavailable opportunity to discover novel leukocyte regulatory networks in critically injured patients. Severe injury induced significant changes in the T-cell, monocyte, and total leukocyte transcriptome, with only 12% of these genomic changes common to all three cell populations. T-cell-specific pathway analyses identified increased gene expression of several novel inhibitory receptors (PD-1, CD152, NRP-1, Lag3), and concomitant decreases in stimulatory receptors (CD28, CD4, IL-2Ralpha). Functional analysis of T-cells and monocytes confirmed reduced T-cell proliferation and increased cell surface expression of negative signaling receptors paired with decreased monocyte costimulation ligands. Thus, genome-wide expression from highly-enriched cell populations combined with knowledge-based pathway analyses leads to the identification of novel regulatory networks differentially expressed in injured patients. Importantly, application of cell separation, genome-wide expression, and cell specific pathway analyses can be used to discover novel pathway alterations in human disease. Keywords: Gene expression profiling of circulating total blood leukocytes, T-Cells, and Monocytes in severe trauma patients and healthy subjects.
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Overall design |
Type of experiment: Gene expression profiling of circulating total blood leukocytes, T-Cells, and Monocytes in severe trauma patients and healthy subjects. Experimental factors: Healthy subjects, 7 severely traumatized patients and 7 healthy subjects for transcriptome analysis. Venous blood samples were collected. Total blood leukocytes were isolated, and T-cell and monocyte populations were obtained from two subsequent aliquots of the leukocytes. Total leukocytes, enriched T-cells, and enriched monocytes were analyzed using Affymetrix GeneChip arrays. Number of hybridizations: 42 Human U133A GeneChip arrays (Affymetrix)
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Web link |
http://www.gluegrant.org/pubsupport/supplement-3
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Contributor(s) |
Laudanski K, Miller-Graziano C, Xiao W, Mindrinos MN, Richards DR, De A, Moldawer LL, Maier RV, Bankey P, Baker HV, Brownstein BH, Cobb JP, Calvano SE, Davis RW, Tompkins RG |
Citation(s) |
17032758 |
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Submission date |
Aug 23, 2006 |
Last update date |
Aug 10, 2018 |
Contact name |
Wenzhong Xiao, Inflammation & the Host Response to Injury |
E-mail(s) |
[email protected]
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Phone |
617 726 0082
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Organization name |
Massachusetts General Hospital
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Department |
Department of Surgery
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Lab |
Burn & Trauma Research
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Street address |
55 Fruit Street, GRV 1302
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City |
Boston |
State/province |
MA |
ZIP/Postal code |
02114 |
Country |
USA |
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Platforms (1) |
GPL96 |
[HG-U133A] Affymetrix Human Genome U133A Array |
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Samples (42)
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Relations |
BioProject |
PRJNA95443 |
Supplementary file |
Size |
Download |
File type/resource |
GSE5580_RAW.tar |
145.4 Mb |
(http)(custom) |
TAR (of CEL) |
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