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Transcriptome Analysis of Cultured Limbal Epithelial Cells on an Intact Amniotic Membrane following Hypothermic Storage in Optisol-GS

机译:在Optisol-GS中低温保存后完整羊膜上培养的肢体上皮细胞的转录组分析

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摘要

The aim of the present study was to investigate the molecular mechanisms underlying activation of cell death pathways using genome-wide transcriptional analysis in human limbal epithelial cell (HLEC) cultures following conventional hypothermic storage in Optisol-GS. Three-week HLEC cultures were stored in Optisol-GS for 2, 4, and 7 days at 4 °C. Partek Genomics Suite software v.6.15.0422, (Partec Inc., St. Louis, MO, USA) was used to identify genes that showed significantly different (P < 0.05) levels of expression following hypothermic storage compared to non-stored cell sheets. There were few changes in gene expression after 2 days of storage, but several genes were differently regulated following 4 and 7 days of storage. The histone-coding genes HIST1H3A and HIST4H4 were among the most upregulated genes following 4 and 7 days of hypothermic storage. Bioinformatic analysis suggested that these two genes are involved in a functional network highly associated with cell death, necrosis, and transcription of RNA. HDAC1, encoding histone deacetylase 1, was the most downregulated gene after 7 days of storage. Together with other downregulated genes, it is suggested that HDAC1 is involved in a regulating network significantly associated with cellular function and maintenance, differentiation of cells, and DNA repair. Our data suggest that the upregulated expression of histone-coding genes together with downregulated genes affecting cell differentiation and DNA repair may be responsible for increased cell death following hypothermic storage of cultured HLEC. In summary, our results demonstrated that a higher number of genes changed with increasing storage time. Moreover, in general, larger differences in absolute gene expression values were observed with increasing storage time. Further understanding of these molecular mechanisms is important for optimization of storage technology for limbal epithelial sheets.
机译:本研究的目的是在Optisol-GS中常规低温保存后,使用人全缘上皮细胞(HLEC)培养物中的全基因组转录分析,研究激活细胞死亡途径的分子机制。将三周的HLEC培养物在4°C下储存在Optisol-GS中2、4和7天。使用Partek Genomics Suite软件v.6.15.0422(Partec Inc.,美国密苏里州圣路易斯)来鉴定与低温保存的细胞片相比低温保存后表达水平显着不同(P <0.05)的基因。 。储存2天后基因表达几乎没有变化,但是储存4天和7天后几个基因受到不同的调节。在低温保存4天和7天后,组蛋白编码基因HIST1H3A和HIST4H4是上调程度最高的基因之一。生物信息学分析表明,这两个基因参与了与细胞死亡,坏死和RNA转录高度相关的功能网络。编码组蛋白脱乙酰基酶1的HDAC1是储存7天后表达最下调的基因。与其他下调的基因一起,表明HDAC1参与了与细胞功能和维持,细胞分化以及DNA修复显着相关的调节网络。我们的数据表明,组蛋白编码基因的表达上调与影响细胞分化和DNA修复的基因下调可能是培养的HLEC低温保存后细胞死亡增加的原因。总之,我们的结果表明,随着存储时间的增加,更多的基因发生了变化。而且,通常,随着保存时间的增加,在绝对基因表达值中观察到较大的差异。进一步了解这些分子机制对于优化角膜缘上皮细胞片的存储技术很重要。

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