AI Article Synopsis

  • Retinal degeneration is a key issue in eye disorders, and Mesenchymal Stem Cells (MSCs) show promise in treating these conditions by delivering therapeutic agents like erythropoietin (EPO) to protect retinal neurons.
  • Through the study, human MSCs from umbilical cord tissue were genetically modified and used to create a medium that improved cell viability in retinal neuron models exposed to harmful stressors like glutamate.
  • The findings suggest that MSCs can effectively deliver therapeutic genes, opening up potential new avenues for treating retinal degeneration.

Article Abstract

Retinal degeneration is a prominent feature in ocular disorders. In exploring possible treatments, Mesenchymal Stem Cells (MSCs) have been recognized to yield therapeutic role for retinal degenerative diseases. Studies have also displayed that erythropoietin (EPO) administration into degenerative retina models confers significant neuroprotective actions in limiting pathological cell death. In this study, we aimed to use MSCs to deliver EPO and to evaluate the ability of EPO to rescue retinal neurons from dying upon reactive oxidative stress induction. We derived human MSCs from Wharton's jelly (hWJMSCs) of the umbilical cord and cells were transduced with lentivirus particles encoding and a reporter gene of green fluorescent protein (). The supernatants of both transduced and non-transduced cells were collected and used as a pre-conditioning medium for Y79 retinoblastoma cells (retinal neuron cell line) following exposure to glutamate induction. Retinal cells exposed to glutamate showed reduced mitochondrial depolarization and enhanced improvement in cell viability when incubated with pre-conditioned media of transduced cells. Our results established a proof-of-concept that MSCs could be used as a candidate for the delivery of therapeutic gene in the treatment of retinal degenerations.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6079241PMC
http://dx.doi.org/10.3389/fncel.2018.00190DOI Listing

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