4.3 Article

Inhibition by miR-410 facilitates direct retinal pigment epithelium differentiation of umbilical cord blood-derived mesenchymal stem cells

期刊

JOURNAL OF VETERINARY SCIENCE
卷 18, 期 1, 页码 59-65

出版社

KOREAN SOC VETERINARY SCIENCE
DOI: 10.4142/jvs.2017.18.1.59

关键词

microRNA; miR-410; retinal pigment epithelium; umbilical cord blood-derived mesenchymal stem cells

资金

  1. Korea Health Technology R&D Project through the Korea Health Industry Development Institute (KHIDI)-Ministry of Health & Welfare, Republic of Korea [11114C3301]
  2. Research Institute for Veterinary Science, Seoul National University (Republic of Korea)

向作者/读者索取更多资源

Retinal pigment epithelium (RPE) is a major component of the eye. This highly specialized cell type facilitates maintenance of the visual system. Because RPE loss induces an irreversible visual impairment, RPE generation techniques have recently been investigated as a potential therapeutic approach to RPE degeneration. The microRNA-based technique is a new strategy for producing RPE cells from adult stem cell sources. Previously, we identified that antisense microRNA-410 (anti-miR-410) induces RPE differentiation from amniotic epithelial stem cells. In this study, we investigated RPE differentiation from umbilical cord blood -derived mesenchymal stem cells (UCB-MSCs) via anti-miR-410 treatment. We identified miR-410 as a RPE-relevant microRNA in UCB-MSCs from among 21 putative human RPE-depleted microRNAs. Inhibition of miR-410 induces overexpression of immature and mature RPE-specific factors, including MITF, LRAT, RPE65, Bestrophin, and EMMPRIN. The RPE-induced cells were able to phagocytize microbeads. Results of our microRNA-based strategy demonstrated proof-of-principle for RPE differentiation in UCB-MSCs by using anti-miR-410 treatment without the use of additional factors or exogenous transduction.

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