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Ascorbic Acid Promotes the Stemness of Corneal Epithelial Stem/Progenitor Cells and Accelerates Epithelial Wound Healing in the Cornea

机译:抗坏血酸促进角膜上皮干细胞/祖细胞的干性,并加速角膜上皮的伤口愈合。

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摘要

High concentration of ascorbic acid (vitamin C) has been found in corneal epithelium of various species. However, the specific functions and mechanisms of ascorbic acid in the repair of corneal epithelium are not clear. In this study, it was found that ascorbic acid accelerates corneal epithelial wound healing in vivo in mouse. In addition, ascorbic acid enhanced the stemness of cultured mouse corneal epithelial stem/progenitor cells (TKE2) in vitro, as shown by elevated clone formation ability and increased expression of stemness markers (especially p63 and SOX2). The contribution of ascorbic acid on the stemness enhancement was not dependent on the promotion of Akt phosphorylation, as concluded by using Akt inhibitor, nor was the stemness found to be dependent on the regulation of oxidative stress, as seen by the use of two other antioxidants (GMEE and NAC). However, ascorbic acid was found to promote extracellular matrix (ECM) production, and by using two collagen synthesis inhibitors (AzC and CIS), the increased expression of p63 and SOX2 by ascorbic acid was decreased by around 50%, showing that the increased stemness by ascorbic acid can be attributed to its regulation of ECM components. Moreover, the expression of p63 and SOX2 was elevated when TKE2 cells were cultured on collagen I coated plates, a situation that mimics the in vivo situation as collagen I is the main component in the corneal stroma. This study shows direct therapeutic benefits of ascorbic acid on corneal epithelial wound healing and provides new insights into the mechanisms involved.
机译:在各种物种的角膜上皮中发现了高浓度的抗坏血酸(维生素C)。但是,抗坏血酸在角膜上皮修复中的具体功能和机制尚不清楚。在这项研究中,发现抗坏血酸在小鼠体内可加速角膜上皮伤口的愈合。此外,抗坏血酸增强了体外培养的小鼠角膜上皮干/祖细胞(TKE2)的干性,如克隆形成能力增强和干性标志物(尤其是p63和SOX2)的表达增强所表明的。如使用Akt抑制剂所得出的结论,抗坏血酸对茎增强的贡献不取决于促进Akt磷酸化,也不如通过使用其他两种抗氧化剂看到的那样,茎抗取决于氧化应激的调节(GMEE和NAC)。然而,发现抗坏血酸促进细胞外基质(ECM)的产生,并且通过使用两种胶原蛋白合成抑制剂(AzC和CIS),抗坏血酸使p63和SOX2的表达增加减少了约50%,表明增加的干度抗坏血酸的作用可以归因于其对ECM成分的调节。而且,当在胶原蛋白I包被的板上培养TKE2细胞时,p63和SOX2的表达升高,这种情况模仿了体内情况,因为胶原蛋白I是角膜基质中的主要成分。这项研究显示了抗坏血酸对角膜上皮伤口愈合的直接治疗作用,并为涉及的机制提供了新见解。

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