Grant: Discovery Grants Program - Individual
University of Western Ontario
$35,858.00
Biology of cell-surface interactions
FY 2012-13
Summary
In organs and tissues of the human body, cells adhere to a complex scaffold-like protein mesh called the extracellular matrix (ECM). The ECM provides cells with many stimuli and signals that cells need to behave normally. However, sometimes cells are forced to come into contact with artificial materials. Central in many bioengineering applications is the attachment of human cells to artificial materials, but the factors important in successful cell-material attachment are not well understood. Our previous research has identified that the topography and chemistry of materials can be altered to enhance cell attachment. When a cell attaches to a surface, it results in activation of important signaling molecules required by the cells to survive. Cells attach to surfaces through specialized sites called focal adhesions (FA), and research is highlighting that these adhesions are very important sites in cells. FAs are responsible for relaying the attachment event to other areas within the cells that control normal cell behaviour. We hypothesize that by altering the chemistry and topography of the materials, we can enhance the function of human fibroblasts. Using techniques harnessed from the microelectronic industry, it has become possible to produce structures with precisely defined surfaces for cell-biological studies, thus allowing the reaction of cells to defined topographic and chemical features to be observed. The aim of our research is 1) to investigate the interactions of human fibroblasts with nano- and micro-metric repeating groove topographies, 2) to quantify matrix assembly and tissue development by fibroblasts on nano- and micro-metric repeating groove topographies. The results of the study will directly address how cells transmit external stimuli into signals that regulate their normal behaviour, which will be important for all areas of cell biology. We anticipate that the information produced by our program could in the long term be used in cell and tissue engineering applications, where our lack of understanding of cell-material interactions are limiting the development of engineered tissue substitutes.
Program
Discovery Grants Program - Individual
Recipient
Location
Ontario, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data
As published
Application id
355615-2009
Name nom
Hamilton, Douglas
Department département
Anatomy and Cell Biology
Organization id
36
Institution établissement
University of Western Ontario
Province en
Ontario
Province fr
Ontario
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2012
Competition year année de concours
2009
Award amount
35858
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
1201
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Life sciences (including biotechnology)
Area of application fr
Sciences de la vie (y compris biotechnologie)
Research subject code
5100
Research subject group en
Cell biology
Research subject group fr
Biologie cellulaire
Research subject en
Cell biology
Research subject fr
Biologie cellulaire
Partie
4
Nb partie
5
Application title
Biology of cell-surface interactions
Keyword
NSERC
Application summary
In organs and tissues of the human body, cells adhere to a complex scaffold-like protein mesh called the extracellular matrix (ECM). The ECM provides cells with many stimuli and signals that cells need to behave normally. However, sometimes cells are forced to come into contact with artificial materials. Central in many bioengineering applications is the attachment of human cells to artificial materials, but the factors important in successful cell-material attachment are not well understood. Our previous research has identified that the topography and chemistry of materials can be altered to enhance cell attachment. When a cell attaches to a surface, it results in activation of important signaling molecules required by the cells to survive. Cells attach to surfaces through specialized sites called focal adhesions (FA), and research is highlighting that these adhesions are very important sites in cells. FAs are responsible for relaying the attachment event to other areas within the cells that control normal cell behaviour. We hypothesize that by altering the chemistry and topography of the materials, we can enhance the function of human fibroblasts. Using techniques harnessed from the microelectronic industry, it has become possible to produce structures with precisely defined surfaces for cell-biological studies, thus allowing the reaction of cells to defined topographic and chemical features to be observed. The aim of our research is 1) to investigate the interactions of human fibroblasts with nano- and micro-metric repeating groove topographies, 2) to quantify matrix assembly and tissue development by fibroblasts on nano- and micro-metric repeating groove topographies. The results of the study will directly address how cells transmit external stimuli into signals that regulate their normal behaviour, which will be important for all areas of cell biology. We anticipate that the information produced by our program could in the long term be used in cell and tissue engineering applications, where our lack of understanding of cell-material interactions are limiting the development of engineered tissue substitutes.