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Grant: Discovery Grants Program - Individual

Brock University

$32,000.00

Regulation of neural stem cells by retinoic acid and Notch signalling in the regenerating axolotl spinal cord

EF 2023-24

Résumé
The ability to regenerate a functional spinal cord is restricted to only a few vertebrate species, foremost among them tailed amphibians such as newts and salamanders, and some bony fish. The complex processes that underlie this ability in "regeneration-competent" species is still largely unknown. We are proposing to use the Mexican axolotl, a well-established regeneration-competent amphibian, to examine how spinal cord regeneration works. Based on our previous research, we plan to examine two communication pathways that coordinate interactions between cells during regeneration: the retinoic acid (RA) and Notch pathways. We will do this by using genetically modified "transgenic" axolotl larvae to identify and visualize the cellular sites of activity of multiple nuclear receptors for RA signaling in a key population of spinal cord cells - the ependymoglial (EG) neural stem cells. We will bring to bear newly developed `optogenetic' methods that will enable us to use light to regulate the communication events that occur in EG cells at various times during normal spinal cord regeneration. Importantly, our work will be the first to examine, at this level, how some intercellular communication networks are coordinated during spinal cord regeneration. All of this work will be performed by MSc and PhD students, who will receive valuable training in cutting edge methods in spinal cord research. Through the course of our work we will develop new research tools that will be shared with the spinal cord research community in Canada and abroad. We hope to make important new discoveries that can begin to unravel the complex signaling pathways that lead to regeneration competence in these species and which could shed light on why mammals have lost this ability during evolution.
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
RGPIN-2019-06380
Name nom
Carlone, Robert
Department département
Biological Sciences
Organization id
22
Institution établissement
Brock University
Province en
Ontario
Province fr
Ontario
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2023
Competition year année de concours
2019
Award amount
32000
Program id
RGPIN
Program name en
Discovery Grants Program - Individual
Program name fr
Programme de subventions à la découverte - individuelles
Group en
DISCOVERY RESEARCH
Group fr
RECHERCHE AXÉE SUR LA DÉCOUVERTE
Committee code
1501
Committee name en
Genes, Cells and Molecules
Committee name fr
Gènes, cellules et molécules
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
5111
Research subject group en
Cell biology
Research subject group fr
Signal transduction
Research subject en
Biologie cellulaire
Research subject fr
Transduction de signal
Application title
Regulation of neural stem cells by retinoic acid and Notch signalling in the regenerating axolotl spinal cord
Keyword
axolotl; ependymoglia; Notch; optogenetic; regeneration; retinoic acid; spinal cord; transgenic
Application summary
The ability to regenerate a functional spinal cord is restricted to only a few vertebrate species, foremost among them tailed amphibians such as newts and salamanders, and some bony fish. The complex processes that underlie this ability in "regeneration-competent" species is still largely unknown. We are proposing to use the Mexican axolotl, a well-established regeneration-competent amphibian, to examine how spinal cord regeneration works. Based on our previous research, we plan to examine two communication pathways that coordinate interactions between cells during regeneration: the retinoic acid (RA) and Notch pathways. We will do this by using genetically modified "transgenic" axolotl larvae to identify and visualize the cellular sites of activity of multiple nuclear receptors for RA signaling in a key population of spinal cord cells - the ependymoglial (EG) neural stem cells. We will bring to bear newly developed `optogenetic' methods that will enable us to use light to regulate the communication events that occur in EG cells at various times during normal spinal cord regeneration. Importantly, our work will be the first to examine, at this level, how some intercellular communication networks are coordinated during spinal cord regeneration. All of this work will be performed by MSc and PhD students, who will receive valuable training in cutting edge methods in spinal cord research. Through the course of our work we will develop new research tools that will be shared with the spinal cord research community in Canada and abroad. We hope to make important new discoveries that can begin to unravel the complex signaling pathways that lead to regeneration competence in these species and which could shed light on why mammals have lost this ability during evolution.