Grant: Project Grant
University of Toronto
$504,900.00
The molecular basis of Müller cell dedifferentiation during retinal regeneration
EF 2019-20
Résumé
Humans exhibit a poor ability to regenerate photoreceptors in response to injury or disease. In contrast, other animals, like zebrafish, are capable of regenerating photoreceptors. The regenerative response in zebrafish is mediated by Müller glial cells, which are normally quiescent cells (i.e., they do not divide) and are thought to acquire stem cell characteristics by reprogramming their genome in a process called dedifferentiation in order to replace the lost photoreceptors and ultimately restore vision. However, not all Müller cells participate in the regenerative response and those that do have very limited cell division, and this is presumably to control the numbers of new cells that are produced. In general, the behaviour of Müller cells during dedifferentiation in zebrafish, arguably the best model system to study retinal regeneration, is poorly understood.
We aim to capitalize on the natural regenerative ability of Müller cells in zebrafish in order to gain insight into how dedifferentiation is regulated. Specifically, we aim to: (1) Test if genes related to wound repair affect Müller cell shape changes and function in response to a lesion; and (2) Characterize the role of gene networks that control how Müller cells make the decision to divide.
Although some regenerative properties are evident in human Müller cells, these cells do not produce new photoreceptors in vivo. Our research will allow us to discover new methods for overcoming the barriers to human Müller cell reprogramming into an active stem cell state. In the long term, this could facilitate the development of new pre-clinical models of human retinal regeneration and bring us closer to an endogenous repair strategy for treating blindness.
Programme
Project Grant
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
419978
Name
Tropepe Vincent
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Genetics
Theme2
Biomedical
Prcname2
Developmental Biology
Projecttitle
The molecular basis of Müller cell dedifferentiation during retinal regeneration
Programtype2
Operating Grants
Orgnameinp2
University of Toronto
Cihramount2
$504,900
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Clipseq; Gene Editing; Neurogenesis; Regeneration; Retina; Stem Cell; Transgenic; Wound Repair; Zebrafish
Abstract
Humans exhibit a poor ability to regenerate photoreceptors in response to injury or disease. In contrast, other animals, like zebrafish, are capable of regenerating photoreceptors. The regenerative response in zebrafish is mediated by Müller glial cells, which are normally quiescent cells (i.e., they do not divide) and are thought to acquire stem cell characteristics by reprogramming their genome in a process called dedifferentiation in order to replace the lost photoreceptors and ultimately restore vision. However, not all Müller cells participate in the regenerative response and those that do have very limited cell division, and this is presumably to control the numbers of new cells that are produced. In general, the behaviour of Müller cells during dedifferentiation in zebrafish, arguably the best model system to study retinal regeneration, is poorly understood.
We aim to capitalize on the natural regenerative ability of Müller cells in zebrafish in order to gain insight into how dedifferentiation is regulated. Specifically, we aim to: (1) Test if genes related to wound repair affect Müller cell shape changes and function in response to a lesion; and (2) Characterize the role of gene networks that control how Müller cells make the decision to divide.
Although some regenerative properties are evident in human Müller cells, these cells do not produce new photoreceptors in vivo. Our research will allow us to discover new methods for overcoming the barriers to human Müller cell reprogramming into an active stem cell state. In the long term, this could facilitate the development of new pre-clinical models of human retinal regeneration and bring us closer to an endogenous repair strategy for treating blindness.
Competitiondate
202003
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Tropepe, Vincent
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $504,900~ $0~