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缺氧和α-酮戊二酸对巩膜成纤维细胞胶原蛋白表达的分子机制

Molecular mechanism of hypoxia and alpha-ketoglutaric acid on collagen expression in scleral fibroblasts.

作者信息

Sun Yun, Li Zhuo-Zheng, Yang Jing, Sha Ya-Ru, Hou Xin-Yu, Fu Hong, Li Jia-Yin, Bai Shu-Chang, Xie Yong-Fang, Wang Guo-Hui

机构信息

School of Life Science and Technology, Shandong Second Medical University, Weifang 261053, Shandong Province, China.

出版信息

Int J Ophthalmol. 2024 Oct 18;17(10):1780-1790. doi: 10.18240/ijo.2024.10.03. eCollection 2024.

Abstract

AIM

To investigate the molecular mechanisms underlying the influence of hypoxia and alpha-ketoglutaric acid (α-KG) on scleral collagen expression.

METHODS

Meta-analysis and clinical statistics were used to prove the changes in choroidal thickness (ChT) during myopia. The establishment of a hypoxic myopia model (HYP) for rabbit scleral fibroblasts through hypoxic culture and the effects of hypoxia and α-KG on collagen expression were demonstrated by Sirius red staining. Transcriptome analysis was used to verify the genes and pathways that hypoxia and α-KG affect collagen expression. Finally, real-time quantitative reverse transcription polymerase chain reaction (RT-qPCR) was used for reverse verification.

RESULTS

Meta-analysis results aligned with clinical statistics, revealing a thinning of ChT, leading to scleral hypoxia. Sirius red staining indicated lower collagen expression in the HYP group and higher collagen expression in the HYP+α-KG group, showed that hypoxia reduced collagen expression in scleral fibroblasts, while α-KG can elevated collagen expression under HYP conditions. Transcriptome analysis unveiled the related genes and signaling pathways of hypoxia and α-KG affect scleral collagen expression and the results were verified by RT-qPCR.

CONCLUSION

The potential molecular mechanisms through which hypoxia and α-KG influencing myopia is unraveled and three novel genes , , and are identified. These findings provide a new perspective on the prevention and treatment of myopia regulating collagen expression.

摘要

目的

探讨缺氧和α-酮戊二酸(α-KG)对巩膜胶原表达影响的分子机制。

方法

采用荟萃分析和临床统计来证实近视期间脉络膜厚度(ChT)的变化。通过缺氧培养建立兔巩膜成纤维细胞缺氧近视模型(HYP),并通过天狼星红染色证明缺氧和α-KG对胶原表达的影响。利用转录组分析来验证缺氧和α-KG影响胶原表达的基因和通路。最后,使用实时定量逆转录聚合酶链反应(RT-qPCR)进行反向验证。

结果

荟萃分析结果与临床统计一致,显示ChT变薄,导致巩膜缺氧。天狼星红染色表明HYP组胶原表达较低,而HYP+α-KG组胶原表达较高,表明缺氧降低了巩膜成纤维细胞中的胶原表达,而α-KG可在缺氧条件下提高胶原表达。转录组分析揭示了缺氧和α-KG影响巩膜胶原表达的相关基因和信号通路,结果通过RT-qPCR得到验证。

结论

阐明了缺氧和α-KG影响近视的潜在分子机制,并鉴定出三个新基因 、 和 。这些发现为通过调节胶原表达预防和治疗近视提供了新的视角。

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