Grant: DRA : Canada Graduate Research Scholarship - Doctoral Program (CGRS D)
University of British Columbia
$120,000.00
Comprehensive Investigation of Molecular Mechanisms and Therapeutic Potential of Extracellular Granzyme B in Pterygium
EF 2025-26
Résumé
Pterygium is a common eye disease where a fleshy growth forms on the white part of the eye and can grow onto the cornea, the clear front window of the eye. This growth can cause discomfort, blurred vision, and vision loss. It affects more than 100 million people worldwide, especially those who are older and live in sunny climates where ultraviolet (UV) rays from sunlight are stronger. Currently, surgery is the main treatment, but the fleshy growth often returns after removal, and there are no effective drug treatments. Research shows that inflammation, tissue scarring, abnormal blood vessel growth, and changes in the eye's surface cells all contribute to pterygium. We are studying a protein called granzyme B (GrB), which acts like molecular scissors. GrB is normally used by the immune system to destroy damaged or infected cells. However, when released outside of cells, it can harm healthy tissue by breaking down important structural proteins. Our recent findings show that GrB levels are much higher in pterygium tissues compared to healthy eyes. We also found that certain immune cells, such as mast cells, produce and release GrB. Our other lab experiments show that adding GrB to healthy eye cells makes them more mobile and causes changes similar to those seen in pterygium. In this project, we will examine eye tissues from patients with pterygium to find out which other cells produce and release GrB, what triggers its release (like aging or UV exposure), and how it might cause eye damage. We will also test whether blocking GrB can prevent or reduce these harmful effects. By better understanding how GrB contributes to pterygium, this research may lead to the development of new drug-based treatments for the disease. Because GrB is also involved in other conditions like immune disorders, aging-related diseases, and cancer, our findings could help researchers in many fields.
Programme
DRA : Canada Graduate Research Scholarship - Doctoral Program (CGRS D)
Bénéficiaire
Emplacement
British Columbia, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
560049
Name
Hosseini Amirali
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Neurosciences, Mental Health and Addiction
Theme2
Biomedical
Prcname2
DT1 (Biomedical and/or Clinical Research) CGRS Doctoral
Projecttitle
Comprehensive Investigation of Molecular Mechanisms and Therapeutic Potential of Extracellular Granzyme B in Pterygium
Programtype2
Studentship Programs
Orgnameinp2
University of British Columbia
Cihramount2
$120,000
Cihrequipment2
$0
Programname2
DRA : Canada Graduate Research Scholarship - Doctoral Program (CGRS D)
Keyworddelim
Aging Eye; Granzyme B; Immune Cell Characterization; In Vitro And Ex Vivo Models; Neovascularization And Fibrosis; Ocular Surface; Ocular Surface Squamous Neoplasia; Pterygium; Therapeutics; Ultraviolet Exposure
Abstract
Pterygium is a common eye disease where a fleshy growth forms on the white part of the eye and can grow onto the cornea, the clear front window of the eye. This growth can cause discomfort, blurred vision, and vision loss. It affects more than 100 million people worldwide, especially those who are older and live in sunny climates where ultraviolet (UV) rays from sunlight are stronger. Currently, surgery is the main treatment, but the fleshy growth often returns after removal, and there are no effective drug treatments. Research shows that inflammation, tissue scarring, abnormal blood vessel growth, and changes in the eye's surface cells all contribute to pterygium. We are studying a protein called granzyme B (GrB), which acts like molecular scissors. GrB is normally used by the immune system to destroy damaged or infected cells. However, when released outside of cells, it can harm healthy tissue by breaking down important structural proteins. Our recent findings show that GrB levels are much higher in pterygium tissues compared to healthy eyes. We also found that certain immune cells, such as mast cells, produce and release GrB. Our other lab experiments show that adding GrB to healthy eye cells makes them more mobile and causes changes similar to those seen in pterygium. In this project, we will examine eye tissues from patients with pterygium to find out which other cells produce and release GrB, what triggers its release (like aging or UV exposure), and how it might cause eye damage. We will also test whether blocking GrB can prevent or reduce these harmful effects. By better understanding how GrB contributes to pterygium, this research may lead to the development of new drug-based treatments for the disease. Because GrB is also involved in other conditions like immune disorders, aging-related diseases, and cancer, our findings could help researchers in many fields.
Competitiondate
202511
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Hosseini, Amirali
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $120,000~ $0~