Grant: Doctoral Award - Frederick Banting and Charles Best Canada Graduate Scholarships
University of British Columbia
$105,000.00
Treating retinal degeneration with stem cells - a multifaceted approach
EF 2012-13
Résumé
Retinal degenerative diseases can be devastating, as they can take away one's primary ability to interact with the world around them. The most common of these diseases is age-related macular degeneration (AMD), which affects nearly 600,000 Canadians and over 14 million people worldwide, with these figures continuing to rise given our aging population and increasing life-spans. Though remarkable progress has been made in the treatment of 'wet' AMD, the other 'dry' form, which accounts for over 90% of all AMD, has no effective treatment and there is little-to-no understanding of its underlying cause. In many retinal degenerative diseases, photoreceptors atrophy and then die off, while the neighboring network of neurons that mediate the passage of visual signals to the brain remain largely intact. In light of this, scientists have attempted to use stem cells to regenerate these photoreceptors, as stem cells have the unique ability to differentiate into any desired cell type when treated with the correct growth factors. Unfortunately, preclinical trials using stem-cell derived photoreceptor precursor cells (PPCs) to regenerate the retina have resulted in too few cells staying at the desired site in the retina, and those that remain rarely integrate - form connections with downstream neurons. The problem is that PPCs are dispersing from where they are needed most, and the majority of those that remain fail to live long enough to form synapses. To address this, I propose to utilize novel materials that gel once inside the eye as a vehicle for PPCs, thereby retaining them at the site of injection. I also propose to harness the neuroprotective effects of mesenchymal stem cells (MSCs) by co-injecting them with PPCs, which should increase PPC survival, while the addition of synapse-promoting factors should lead to greater integration. My research will help lead to an effective therapy that restores the sight of the many Canadians suffering from advance retinal degeneration.
Programme
Doctoral Award - Frederick Banting and Charles Best Canada Graduate Scholarships
Bénéficiaire
Emplacement
British Columbia, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
283832
Name
Laver Christopher R
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Aging
Theme2
Biomedical
Prcname2
Doctoral Research Awards - A
Projecttitle
Treating retinal degeneration with stem cells - a multifaceted approach
Programtype2
Studentship Programs
Orgnameinp2
University of British Columbia
Cihramount2
$105,000
Cihrequipment2
$0
Programname2
Doctoral Award - Frederick Banting and Charles Best Canada Graduate Scholarships
Keyworddelim
Electroretinography (Erg); Human Embryonic Stem Cells (Hescs); Liposomal Gene Therapy; Mesenchymal Stem Cells (Mscs); Optical Coherence Tamography (Oct); Optokinetic Tracking (Okt); Photoreceptor Precursor Cells (Ppcs); Retinal Degeneration; Stem-Cell Based Retinal Theraputics; Subretinal Injection Of Ppcs And Mscs
Abstract
Retinal degenerative diseases can be devastating, as they can take away one's primary ability to interact with the world around them. The most common of these diseases is age-related macular degeneration (AMD), which affects nearly 600,000 Canadians and over 14 million people worldwide, with these figures continuing to rise given our aging population and increasing life-spans. Though remarkable progress has been made in the treatment of 'wet' AMD, the other 'dry' form, which accounts for over 90% of all AMD, has no effective treatment and there is little-to-no understanding of its underlying cause. In many retinal degenerative diseases, photoreceptors atrophy and then die off, while the neighboring network of neurons that mediate the passage of visual signals to the brain remain largely intact. In light of this, scientists have attempted to use stem cells to regenerate these photoreceptors, as stem cells have the unique ability to differentiate into any desired cell type when treated with the correct growth factors. Unfortunately, preclinical trials using stem-cell derived photoreceptor precursor cells (PPCs) to regenerate the retina have resulted in too few cells staying at the desired site in the retina, and those that remain rarely integrate - form connections with downstream neurons. The problem is that PPCs are dispersing from where they are needed most, and the majority of those that remain fail to live long enough to form synapses. To address this, I propose to utilize novel materials that gel once inside the eye as a vehicle for PPCs, thereby retaining them at the site of injection. I also propose to harness the neuroprotective effects of mesenchymal stem cells (MSCs) by co-injecting them with PPCs, which should increase PPC survival, while the addition of synapse-promoting factors should lead to greater integration. My research will help lead to an effective therapy that restores the sight of the many Canadians suffering from advance retinal degeneration.
Competitiondate
201210
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Laver, Christopher R
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $105,000~ $0~