| Literature DB >> 33505962 |
Tu Nguyen1,2, Daniel Urrutia-Cabrera1,2, Roxanne Hsiang-Chi Liou1,2, Chi D Luu1,2, Robyn Guymer1,2, Raymond Ching-Bong Wong1,2.
Abstract
Age-related macular degeneration (AMD) is the most common cause of irreversible vision loss in people over 50 years old in developed countries. Currently, we still lack a comprehensive understanding of the genetic factors contributing to AMD, which is critical to identify effective therapeutic targets to improve treatment outcomes for AMD patients. Here we discuss the latest technologies that can facilitate the identification and functional study of putative genes in AMD pathology. We review improved genomic methods to identify novel AMD genes, advances in single cell transcriptomics to profile gene expression in specific retinal cell types, and summarize recent development of in vitro models for studying AMD using induced pluripotent stem cells, organoids and biomaterials, as well as new molecular technologies using CRISPR/Cas that could facilitate functional studies of AMD-associated genes.Entities:
Keywords: CRISPR/Cas; age-related macular degeneration; induced pluripotent stem cell models; organoids; retina; single cell transcriptomics
Year: 2021 PMID: 33505962 PMCID: PMC7829507 DOI: 10.3389/fcell.2020.604220
Source DB: PubMed Journal: Front Cell Dev Biol ISSN: 2296-634X