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Series GSE5580 Query DataSets for GSE5580
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
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.
 
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)
Web link http://www.gluegrant.org/pubsupport/supplement-3
 
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
Submission date Aug 23, 2006
Last update date Aug 10, 2018
Contact name Wenzhong Xiao, Inflammation & the Host Response to Injury
E-mail(s) data_curator@gluegrant.org
Phone 617 726 0082
Organization name Massachusetts General Hospital
Department Department of Surgery
Lab Burn & Trauma Research
Street address 55 Fruit Street, GRV 1302
City Boston
State/province MA
ZIP/Postal code 02114
Country USA
 
Platforms (1)
GPL96 [HG-U133A] Affymetrix Human Genome U133A Array
Samples (42)
GSM129729 C1L
GSM129730 C1M
GSM129731 C1T
Relations
BioProject PRJNA95443

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Supplementary file Size Download File type/resource
GSE5580_RAW.tar 145.4 Mb (http)(custom) TAR (of CEL)

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