Grant: Discovery Grants Program - Individual
University of Western Ontario
$43,100.00
MMP activation during xenopus development
EF 2008-09
Résumé
Animals have evolved numerous ways to grow from a fertilized egg to a reproductive adult. Many developmental strategies and approaches are used, but there are several constants. Among these constants is the need for cell-to-cell communication and interactions. These interactions allow for important signalling events to occur at the correct time and place during development. Interestingly these events in part are regulated by proteins found outside of cells - the extracellular matrix (ECM). The ECM has been recognized for decades, but it is only recently that its importance is clearly understood. The ECM can influence how cells communicate with each other, and so the degradation or remodelling of the ECM will affect this cell-cell communication. These changes and remodelling of the ECM have been observed in diseases such as cancer where secreted enzymes (matrix metalloproteinases, MMPs) were identified that changed the ECM. MMPs are now known to play important roles in development, where they appropriately regulate the structure of the ECM. As MMPs can have profound impacts, their activity is regulated in a number of ways. Most MMPs are secreted outside of cells in an inactive form and are activated when needed. MMPs are often activated by other cell-surface MMPs called MT-MMPs. Intriguingly (and counter intuitively) MT-MMPs work with secreted inhibitors, TIMPs (their inhibitors) to activate other MMPs. This activation process is delicately balanced as an excess of TIMP molecules would inhibit all MT-MMPs and thus stop the activation process. MMPs, MT-MMP and TIMPs individually have important developmental functions. However, very little is known about how they interact with each other to appropriately regulate the remodelling of the ECM during development. This research proposal uses frog as a developmental model with which the functions and interactions of these molecules can be assayed. By understanding their role and how they act during the development of a living organism we can then better understand the underlying mechanisms that play a role in normal and abnormal embryogenesis.
Programme
Discovery Grants Program - Individual
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data
Tel que publié
Application id
238412-2006
Name nom
Damjanovski, Sashko
Department département
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
2008
Competition year année de concours
2006
Award amount
43100
Program id
RGPIN
Program nane 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
33
Committee name en
Molec. & Develop. Genetics
Committee name fr
Gén. moléculaire et dévelop.
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
5106
Research subject group en
Cell biology
Research subject group fr
Biologie cellulaire
Research subject en
Extra-cellular matrix
Research subject fr
Matrice extra-cellulaire
Partie
3
Nb partie
5
Application title
MMP activation during xenopus development
Keyword
NA
Application summary
Animals have evolved numerous ways to grow from a fertilized egg to a reproductive adult. Many developmental strategies and approaches are used, but there are several constants. Among these constants is the need for cell-to-cell communication and interactions. These interactions allow for important signalling events to occur at the correct time and place during development. Interestingly these events in part are regulated by proteins found outside of cells - the extracellular matrix (ECM). The ECM has been recognized for decades, but it is only recently that its importance is clearly understood. The ECM can influence how cells communicate with each other, and so the degradation or remodelling of the ECM will affect this cell-cell communication. These changes and remodelling of the ECM have been observed in diseases such as cancer where secreted enzymes (matrix metalloproteinases, MMPs) were identified that changed the ECM. MMPs are now known to play important roles in development, where they appropriately regulate the structure of the ECM. As MMPs can have profound impacts, their activity is regulated in a number of ways. Most MMPs are secreted outside of cells in an inactive form and are activated when needed. MMPs are often activated by other cell-surface MMPs called MT-MMPs. Intriguingly (and counter intuitively) MT-MMPs work with secreted inhibitors, TIMPs (their inhibitors) to activate other MMPs. This activation process is delicately balanced as an excess of TIMP molecules would inhibit all MT-MMPs and thus stop the activation process. MMPs, MT-MMP and TIMPs individually have important developmental functions. However, very little is known about how they interact with each other to appropriately regulate the remodelling of the ECM during development. This research proposal uses frog as a developmental model with which the functions and interactions of these molecules can be assayed. By understanding their role and how they act during the development of a living organism we can then better understand the underlying mechanisms that play a role in normal and abnormal embryogenesis.