Macrophages are the cornerstone of the innate immune response to infection. They define the nature of pathogens through germ-line encoded pattern recognition receptors that then process the information and specify appropriate responses. The Toll-like receptors are prototypic pattern recognition receptors; TLR4 recognizes the Gram-negative cell-wall component LPS, while TLR5 detects bacterial flagellin. TLR4 and TLR5 trigger both common and distinct signaling pathways in macrophages, and these elicit different responses to different pathogens. To obtain the structure of these pathways we will use isotope-coded affinity tags (ICAT) to quantify early phosphorylation events triggered by TLR4 and TLR5, and correlate these events with specific biological outcomes defined by cDNA arrays representing more than 1600 macrophage inflammatory genes. These data will permit development of a predictive model that will be confirmed and refined by additional perturbations of constriction points in the signaling pathways. This model will be a starting point for the development of a comprehensive network model of macrophage signaling. This approach will ultimately be applicable to a broad array of biological systems.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Clinical Investigator Award (CIA) (K08)
Project #
5K08AI056092-04
Application #
7072622
Study Section
Allergy & Clinical Immunology-1 (AITC)
Program Officer
Prograis, Lawrence J
Project Start
2003-06-01
Project End
2008-05-31
Budget Start
2006-06-01
Budget End
2007-05-31
Support Year
4
Fiscal Year
2006
Total Cost
$126,900
Indirect Cost
Name
Institute for Systems Biology
Department
Type
DUNS #
135646524
City
Seattle
State
WA
Country
United States
Zip Code
98109
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