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Association of Cyclin Dependent Kinase 10 and Transcription Factor 2 during Human Corneal Epithelial Wound Healing in vitro model

机译:人角膜上皮伤口愈合过程中细胞周期蛋白依赖性激酶10和转录因子2的关联

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摘要

Proper wound healing is dynamic in order to maintain the corneal integrity and transparency. Impaired or delayed corneal epithelial wound healing is one of the most frequently observed ocular defect and difficult to treat. Cyclin dependen kinase (cdk), a known cell cycle regulator, required for proper proliferating and migration of cell. We therefore investigated the role of cell cycle regulator cdk10, member of cdk family and its functional association with transcriptional factor (ETS2) at active phase of corneal epithelial cell migration. Our data showed that cdk10 was associated with ETS2, while its expression was upregulated at the active phase (18 hours) of cell migration and gradually decrease as the wound was completely closed. Topical treatment with anti-cdk10 and ETS2 antibodies delayed the wound closure time at higest concentration (10 µg/ml) compared to control. Further, our results also showed increased mRNA expression of cdk10 and ETS2 at active phase of migration at approximately 2 fold. Collectively, our data reveals that cdk10 and ETS2 efficiently involved during corneal wound healing. Further studies are warranted to better understand the mechanism and safety of topical cdk10 and ETS2 proteins in corneal epithelial wound-healing and its potential role for human disease treatment.
机译:适当的伤口愈合是动态的,以保持角膜的完整性和透明度。角膜上皮伤口愈合受损或延迟是最常见的眼部缺陷之一,难以治疗。细胞周期蛋白依赖性激酶(cdk)是已知的细胞周期调节剂,是细胞正常增殖和迁移所必需的。因此,我们研究了角膜上皮细胞迁移活跃期细胞周期调节子cdk10(cdk家族成员)的作用及其与转录因子(ETS2)的功能关联。我们的数据显示cdk10与ETS2相关,而其表达在细胞迁移的活跃阶段(18小时)上调,并随着伤口完全闭合而逐渐降低。与对照相比,在最高浓度(10μg/ ml)下,抗cdk10和ETS2抗体的局部治疗延迟了伤口闭合时间。此外,我们的研究结果还表明,在迁移活跃期,cdk10和ETS2的mRNA表达增加了约2倍。总体而言,我们的数据表明cdk10和ETS2在角膜伤口愈合过程中有效参与。有必要进行进一步的研究,以更好地了解局部cdk10和ETS2蛋白在角膜上皮伤口愈合中的机制和安全性及其在人类疾病治疗中的潜在作用。

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