Grant: Discovery Grants Program - Individual
University of Manitoba
$51,000.00
Investigation of immune cell trafficking in complex cellular environment
EF 2012-13
Résumé
Immune cell trafficking in tissues is crucial for immune responses and is mediated by various environmental cues such as adhesion molecules and chemoattractants. The focus of past research has been on the roles of individual adhesion molecules and chemoattractants in guiding immune cell trafficking, and the biological mechanisms for cells to detect and respond to simplified non-varying adhesion and migration signals. Because cells are exposed to multiple and spatiotemporally varying directing signals in vivo, understanding immune cell trafficking in complex cellular environment is important for both basic science and clinical research. But very few studies have tried to examine such challenging complexities. The long-term goal of my Discovery program aims at integrating cell biology and immunology approaches, biophysical analysis and novel microfluidic tools to achieve a quantitative and systematic understanding of immune cell trafficking in complex cellular environments. In the first granting period, my focus is on understanding immune cell migration in complex chemoattractant fields. I will apply unique microfluidic systems for quantitative analysis of the migratory behaviours of leukocytes in superimposed and dynamically varying chemoattractant fields. Furthermore, I will investigate the underlying molecular mechanisms with the focus on the role of ligand-induced chemoattractant receptor signalling for immune cell migration in response to spatiotemporal chemotactic signals. I will use a combined approach by experimentally examining the effect of several mutated nondesensitizable chemokine receptors in the migration of both primary leukocytes and myeloid cell lines, and through mathematical modelling and computer simulations. The proposed research will generate exciting insights into immune cell migration and chemotaxis in complex chemoattractant fields and will pave the way for understanding the complex interactions between cells and the guiding environment. My research program will contribute significantly to the biology of immune cell trafficking in tissues, which will be highly relevant to a wide range of physiological problems and diseases such as wound healing, autoimmune diseases and cancers.
Programme
Discovery Grants Program - Individual
Bénéficiaire
Emplacement
Manitoba, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data
Tel que publié
Application id
371474-2009
Name nom
Lin, Francis
Department département
Physics and Astronomy
Organization id
19
Institution établissement
University of Manitoba
Province en
Manitoba
Province fr
Manitoba
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2012
Competition year année de concours
2009
Award amount
51000
Program id
RGPIN
Program name en
Discovery Grants Program - Individual
Program name fr
Programme de subventions à la découverte - individuelles
Group en
Discovery grants programs
Group fr
Programmes de subventions à la découverte
Committee code
32
Committee name en
Cell Biology
Committee name fr
Biologie cellulaire
Area of application code
1200
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Advancement of knowledge
Area of application fr
Avancement des connaissances
Research subject code
3113
Research subject group en
Physics
Research subject group fr
Physique
Research subject en
Biophysics
Research subject fr
Biophysique
Partie
4
Nb partie
5
Application title
Investigation of immune cell trafficking in complex cellular environment
Keyword
NSERC
Application summary
Immune cell trafficking in tissues is crucial for immune responses and is mediated by various environmental cues such as adhesion molecules and chemoattractants. The focus of past research has been on the roles of individual adhesion molecules and chemoattractants in guiding immune cell trafficking, and the biological mechanisms for cells to detect and respond to simplified non-varying adhesion and migration signals. Because cells are exposed to multiple and spatiotemporally varying directing signals in vivo, understanding immune cell trafficking in complex cellular environment is important for both basic science and clinical research. But very few studies have tried to examine such challenging complexities. The long-term goal of my Discovery program aims at integrating cell biology and immunology approaches, biophysical analysis and novel microfluidic tools to achieve a quantitative and systematic understanding of immune cell trafficking in complex cellular environments. In the first granting period, my focus is on understanding immune cell migration in complex chemoattractant fields. I will apply unique microfluidic systems for quantitative analysis of the migratory behaviours of leukocytes in superimposed and dynamically varying chemoattractant fields. Furthermore, I will investigate the underlying molecular mechanisms with the focus on the role of ligand-induced chemoattractant receptor signalling for immune cell migration in response to spatiotemporal chemotactic signals. I will use a combined approach by experimentally examining the effect of several mutated nondesensitizable chemokine receptors in the migration of both primary leukocytes and myeloid cell lines, and through mathematical modelling and computer simulations. The proposed research will generate exciting insights into immune cell migration and chemotaxis in complex chemoattractant fields and will pave the way for understanding the complex interactions between cells and the guiding environment. My research program will contribute significantly to the biology of immune cell trafficking in tissues, which will be highly relevant to a wide range of physiological problems and diseases such as wound healing, autoimmune diseases and cancers.