Cellular-Level Evaluation of the Effects of Mesenchymal Stem Cell–Derived Exosomes in a Retinal Pigment Epithelium Culture Model of Proliferative Vitreoretinopathy
Project no. 32123 · Status: Kapanmış (Yayın bekleniyor) · 2024
Summary
<p>The retinal pigment epithelium plays a critical role in maintaining both the anatomical integrity and functional activity of the retinal photoreceptor layer, as well as the continuity of choroidal vascularization. Alterations in retinal pigment epithelium differentiation may lead to various retinal pathologies, including rod-cone dystrophies, inherited macular degeneration, age-related macular degeneration, and proliferative vitreoretinopathy (PVR). Since there is currently no established definitive treatment for PVR, the potential effects of alternative therapeutic approaches, particularly stem cell–based therapies, are being extensively investigated.</p><p>Exosomes secreted by mesenchymal stem cells (MSC-Exos) are phospholipid biomolecular vesicles containing proteins, lipids, and various nucleotides. MSC-Exos have attracted considerable attention as innovative therapeutic agents because of their involvement in a variety of physiological and pathological processes, including neural regeneration, atherosclerosis, fibrosis, and immune regulation. Exosomes, which participate in the transmission of biological signals and can influence the behavior of recipient cells by carrying functional biomolecules, are capable of communicating locally or systemically and may affect various biological processes such as immune responses, tissue regeneration, and disease progression. Investigation of the therapeutic effects of mesenchymal stem cells in ocular disease models has therefore emerged as a current and significant area of research.</p><p>The aim of this study was to investigate the effects of mesenchymal stem cell–derived exosomes on proliferation, apoptosis, and wound healing in an in vitro PVR model. As a result of this research, the cellular effects of MSC-Exos on maintaining retinal pigment epithelium cell function and integrity will be elucidated. In addition, this study is expected to contribute novel insights to the literature regarding PVR modeling and treatment.</p>