Grant: Discovery Grants Program - Individual
Memorial University of Newfoundland
$34,372.00
Mechanisms of action of Hsp27 and stress activated signaling
FY 2008-09
Summary
Heat shock proteins are a class of proteins whose cellular expression can be increased by exposure of the cells to a potentially lethal stress, such as heat shock. One of these proteins is the small heat shock protein called Hsp27. This protein is expressed in a variety of cell types, but my interest is in its role in cells of the nervous system. Our research has shown that this protein can protect neurons from damage from various stressors. However, this protein is also found normal sensory neurons and we do not fully understand its role in the normal cells. It appears to play a role in the ability of these sensory neurons to regenerate after nerve injury. The research we describe in this project is designed to help us understand how Hsp27 can interact with the neuronal cytoskeleton (that is required for regeneration) and how it may contribute to promoting regeneration after damage. Understanding how proteins such as the sHsps function in the normal nervous system, particularly in neurons whose regenerative potential is quite good, will provide basic information on ways in which neuronal growth can be regulated. The normal role of Hsp27 in neurons, particularly those in which it is constitutively expressed, is not fully known; not all neurons express Hsp27 nor can it be induced in all neurons. This suggests that there is something special about its presence in sensory neurons which could be related to the generally very high regenerative potential of peripheral nerve axons, in contrast to that of CNS axons.
Program
Discovery Grants Program - Individual
Recipient
Location
Newfoundland and Labrador, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data
As published
Application id
152940-2008
Name nom
Mearow, Karen
Department département
Medicine, Faculty of
Organization id
89
Institution établissement
Memorial University of Newfoundland
Province en
Newfoundland and Labrador
Province fr
Terre-Neuve-et-Labrador
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2008
Competition year année de concours
2008
Award amount
34372
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
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
5111
Research subject group en
Cell biology
Research subject group fr
Biologie cellulaire
Research subject en
Signal transduction
Research subject fr
Transduction de signal
Partie
1
Nb partie
5
Application title
Mechanisms of action of Hsp27 and stress activated signaling
Keyword
NA
Application summary
Heat shock proteins are a class of proteins whose cellular expression can be increased by exposure of the cells to a potentially lethal stress, such as heat shock. One of these proteins is the small heat shock protein called Hsp27. This protein is expressed in a variety of cell types, but my interest is in its role in cells of the nervous system. Our research has shown that this protein can protect neurons from damage from various stressors. However, this protein is also found normal sensory neurons and we do not fully understand its role in the normal cells. It appears to play a role in the ability of these sensory neurons to regenerate after nerve injury. The research we describe in this project is designed to help us understand how Hsp27 can interact with the neuronal cytoskeleton (that is required for regeneration) and how it may contribute to promoting regeneration after damage. Understanding how proteins such as the sHsps function in the normal nervous system, particularly in neurons whose regenerative potential is quite good, will provide basic information on ways in which neuronal growth can be regulated. The normal role of Hsp27 in neurons, particularly those in which it is constitutively expressed, is not fully known; not all neurons express Hsp27 nor can it be induced in all neurons. This suggests that there is something special about its presence in sensory neurons which could be related to the generally very high regenerative potential of peripheral nerve axons, in contrast to that of CNS axons.