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Grant: Fellowship: Bisby (Prize)

Direct Payment

$12,500.00

Identifying the Molecular Determinants of Axonal Regeneration

EF 2013-14

Résumé
The central nervous system (CNS) is comprised of the brain and spinal cord. CNS injuries are very complicated and unfortunately lead to permanent disability. For example, patients with spinal cord injuries typically spend the rest of their lives confined to a wheelchair. Despite several decades of research in this field there is currently no treatment available for spinal cord injury patients. Researchers and clinicians are trying to find new avenues for enhancing repair and improving outcomes. The main contributing factor is the poor regeneration of axons (essential connections between neurons) in the CNS. This limited axon growth in the CNS is largely due to the inherently inefficient capacity for axons to regrow. The current literature suggests that networks of genes are responsible for their growth but they are not known at this stage. Through this work, I want to explore those genes and the factors regulating them. Once I identify these genes, I wish to manipulate them (by adding and deleting) and thereby transform CNS neurons into an actively growing state. I will introduce these genes into the poorly growing CNS neurons of a mouse strain in order to convert them to robustly growing CNS neurons. Additionally, I will analyse the impact of these factors/genes in an animal model of CNS injury to confirm their impact on recovery. I hope that understanding the mechanisms of regrowth and identifying the responsible genes will help researchers to advance this field and allow them to explore new promises for clinical use.
Programme
Fellowship: Bisby (Prize)
Bénéficiaire
Emplacement
Massachusetts, United States of America
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
308819
Name
Singh Bhagat
Region
Massachusetts
Country
United States of America
Orgtype
Research Institution
Instname2
Neurosciences, Mental Health and Addiction
Theme2
Biomedical
Prcname2
Fellowships - Post-PhD
Projecttitle
Identifying the Molecular Determinants of Axonal Regeneration
Programtype2
Fellowship Programs
Orgnameinp2
Direct Payment
Cihramount2
$12,500
Cihrequipment2
$0
Programname2
Fellowship: Bisby (Prize)
Keyworddelim
Drg Neurons; Nerve Regeneration; Nextgen Sequencing; Optic Nerve Injury; Phosphoproteomics; Transcription Factors
Abstract
The central nervous system (CNS) is comprised of the brain and spinal cord. CNS injuries are very complicated and unfortunately lead to permanent disability. For example, patients with spinal cord injuries typically spend the rest of their lives confined to a wheelchair. Despite several decades of research in this field there is currently no treatment available for spinal cord injury patients. Researchers and clinicians are trying to find new avenues for enhancing repair and improving outcomes. The main contributing factor is the poor regeneration of axons (essential connections between neurons) in the CNS. This limited axon growth in the CNS is largely due to the inherently inefficient capacity for axons to regrow. The current literature suggests that networks of genes are responsible for their growth but they are not known at this stage. Through this work, I want to explore those genes and the factors regulating them. Once I identify these genes, I wish to manipulate them (by adding and deleting) and thereby transform CNS neurons into an actively growing state. I will introduce these genes into the poorly growing CNS neurons of a mouse strain in order to convert them to robustly growing CNS neurons. Additionally, I will analyse the impact of these factors/genes in an animal model of CNS injury to confirm their impact on recovery. I hope that understanding the mechanisms of regrowth and identifying the responsible genes will help researchers to advance this field and allow them to explore new promises for clinical use.
Competitiondate
201311
Approvedterm2
2 yrs 6 mths
Pinamesdelim
Singh, Bhagat
Approvedterm
2 ans 6 mois
Cihrcontribution2
~ $12,500~ $0~