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EFRI- BSBA: Novel microsystems for manipulation and analysis of immune cells  

The goal of the proposal will be the development of novel microsystems for analysis and manipulation of immune cells. Immune cells serve as sentinels of infections, malignancies and autoimmune disorders afflicting an individual. Therefore, these cells may be used to gain diagnostic information as well as to enhance understanding of mechanism of immune disease progression. Analysis of immune cells (leukocytes) represents a singular challenge because there is multiple cell subsets present in the body that are often distinguishable only based on the secreted products. This is true for T-lymphocytes that can be categorized into T-helper 1, T-helper 2 or T-helper 17 phenotype based on the secretion of specific proteins (cytokines). Similarly, B-cells represent a heterogeneous population of cells that are distinguished solely based on the production of specific antibodies. Single cell-level, real-time analysis of products secreted by live T-cells and B-cells is not currently possible due to the lack of appropriate bioanalytical tools. To address this shortcoming, this proposal will develop novel microsystems allowing to arrange immune cells in high density single cell arrays and then monitor production of secreted proteins at a single cell level. In addition, they will develop a "sense-and-release" electrode array system for identifying immune cells based on the secreted product and subsequently sorting/releasing these cells. The microsystems developed in this proposal will be used for the analysis of T-cells from normal and autistic children with the goal of helping to identify correlates between immune function and behavioral aberrations. An individual cell is the smallest living building block of tissues and organs. Therefore, analysis of single living cells has been at the frontier of biological/life science research for the past decade and half. The use of green fluorescence protein (GFP) and other fluorescent proteins to report on dynamics of how and when genes get turned on in individual cells has revolutionized the field of biological and medical sciences. However, the requirement of having to get GFP-encoding DNA into cells limits application of reporter gene technology to the most robust and easy to transfect cells. In addition, reporter gene technology monitors gene expression as opposed to protein production. The vision of this proposal is to develop novel and transformative bio-microsystems for non-invasive, dynamic monitoring of protein production in difficult-to-transfect primary cells. This proposal will focus on the analysis of leukocytes and will develop biosensors and microsystems for monitoring cytokine production of individual T-lymphocytes. The interdisciplinary team of investigators will provide surface engineering and microfabrication-based solutions to challenges that currently confound single cell analysis, including: 1) creating high-density single cell arrays, 2) integrating multi-analyte sensors with single cells, 3) co-localizing sensing elements with single cells to ensure high local concentration of secreted metabolite. The novel biosensors to be developed in this proposal will be translatable to other cellular systems (e.g. circulating as well as anchorage-dependent cells) and will be broadly applicable in bioengineering, biotechnology and life sciences fields. The interdisciplinary collaboration of researchers with a diverse expertise in this project provides a unique opportunity and framework for interdisciplinary education and training of secondary school through postdoctoral students at the frontiers of engineering and the life sciences. Project Status
ONGOING

2010

Funder National Science Foundation
Fiscal Year Funding $524,890.25
Current Award Period 2009-2013
Project Number 937997
Principal Investigator Revzin, Alexander
Received ARRA Funding? No
Strategic Plan Question Question 2: How Can I Understand What Is Happening? (Biology)
Subcategory Immune/Metabolic Pathways
Strategic Plan Objective Green dot: Objective has greater than or equal to the recommended funding. 2SA. Support at least four research projects to identify mechanisms of fever, metabolic and/or immune system interactions with the central nervous system that may influence ASD during prenatal-postnatal life by 2010. IACC Recommended Budget: $9,800,000 over 4 years. (Fever studies to be started by 2012.)
Federal or Private? Federal
Institution University of California, Davis
State/Country California
Web Link 1 EFRI- BSBA: Novel microsystems for manipulation and analysis of immune cells (External web link)
Web Link 2 EFRI- BSBA: Novel microsystems for manipulation and analysis of immune cells (External web link)
Web Link 3 No URL available.
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