在HRMEC中,乳酸结合蛋白DNMT3A通过HIF-1α乳化对VEGFA进行上调,从而促进血管新生
Xiaotang Wang1,2,3, Jiaxing Huang1,2,3, Wei Fan1,2,3
1The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Genome biology
|October 31, 2025
概括
基因甲基转移酶DNMT3A调节蛋白质乳酸和血管内皮生长因子 (VEGF) 的产生,影响眼部新血管化. 针对这种途径为失明提供了新的治疗策略.
科学领域:
- 眼科医生 眼科 眼科
- 分子生物学分子生物学
- 细胞生物学 细胞生物学
背景情况:
- 眼部新血管化是导致失明的主要原因.
- 缺氧诱导的视网膜血管生成涉及乳酸积累和蛋白质乳酸化.
- 连接这些过程的确切机制仍在调查中.
研究的目的:
- 研究DNA甲基转移酶3A (DNMT3A) 在低氧诱导的眼球新血管化过程中调节乳糖化的作用.
- 阐明DNMT3A影响血管生成的机制.
主要方法:
- 研究了氧气诱导的视网膜病变模型.
- 在内皮细胞中评估了DNMT3A,HIF-1α乳酸和VEGF的水平.
- 给出的外源乳酸和抑制的乳酸摄取.
- 调节DNMT3A表达在体外和体内.
主要成果:
- 在视网膜病变期间,DNMT3A水平,HIF-1α乳酸和VEGF增加.
- 乳酸盐的使用增强了血管化;乳酸盐摄取抑制降低了血管生成.
- DNMT3A表达水平与HIF-1α乳酸和血管生成相关.
- DNMT3A促进了核乳酸盐运输,通过HIF-1α乳化促进了VEGFA.
结论:
- DNMT3A对于通过HIF-1α乳化促进VEGFA上调调节来调节血管生成至关重要.
- 乳酸-DNMT3A/HIF-1α乳化/VEGFA途径为眼部新血管化提供了潜在的治疗标.
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