Urine-derived mesenchymal stem cells-derived exosomes enhances survival and proliferation of aging retinal ganglion cells

BMC Molecular and Cell Biology

article

Dan, Qi-Qin¹  Chen, Li¹  shi, Lan-Lan²  Zhou, Xiu³  Wang, Ting-Hua¹  Liu, Hua⁴ 

[1]Institute of Neurological Disease, West China Hospital, Sichuan University

[2]Department of Human Anatomy and Tissue Embryology, Kunming Medical University

[3]Laboratory Animal Department, Institute of Neuroscience, Kunming Medical University

[4]Department of Anatomy, Institute of Eyes, Jinzhou Medical University

关键词: Retinal ganglion cells;    Urine-derived stem cells-derived exosomes;    Aging-related RGCs function loss;    Cell viability and proliferation;   

DOI  :  10.1186/s12860-023-00467-4

学科分类：内科医学

来源: Colegio Oficial de Psicologos

【 摘 要 】

This study was designed to investigate to test the effect of exosomes from urine-derived mesenchymal stem cells (USCs) on the survival and viability of aging retinal ganglion cells (RGCs), and explored the preliminary related mechanisms. Primary USCs were cultured and identified by immunofluorescence staining. Aging RGCs models were established by D-galactose treatment and identified by β-Galactosidase staining. After treatment with USCs conditioned medium (with USCs removal), flow cytometry was performed to examine the apoptosis and cell cycle of RGCs. Cell viability of RGCs was detected by Cell-counting Kit 8 (CCK8) assay. Moreover, gene sequencing and bioinformatics analysis were applied to analyze the genetic variation after medium treatment in RGCs along with the biological functions of differentially expressed genes (DEGs). The number of apoptotic aging RGCs was significantly reduced in USCs medium-treated RGCs. Besides, USCs-derived exosomes exert significant promotion on the cell viability and proliferation of aging RGCs. Further, sequencing data analyzed and identified DEGs expressed in aging RGCs and aging RGCs treated with USCs conditioned medium. The sequencing outcomes demonstrated 117 upregulated genes and 186 downregulated genes in normal RGCs group vs aging RGCs group, 137 upregulated ones and 517 downregulated ones in aging RGCs group vs aging RGCs + USCs medium group. These DEGs involves in numerous positive molecular activities to promote the recovery of RGCs function. Collectively, the therapeutic potentials of USCs-derived exosomes include suppression on cell apoptosis, enhancement on cell viability and proliferation of aging RGCs. The underlying mechanism involves multiple genetic variation and changes of transduction signaling pathways.

【 授权许可】

CC BY|CC0