提达尔吉宁降低抑制剂 降低内皮细胞 血管生成潜力 通过影响 Akt 信号和血管生成因子的表达和分泌
Oskar Ciesielski1,2, Luciano Pirola3, Aneta Balcerczyk4
1Department of Oncobiology and Epigenetics, Faculty of Biology and Environmental Protection, University of Lodz, Pomorska 141/143, Lodz 90-236, Poland.
概括
用PAD抑制剂抑制蛋白质林化减少了内皮细胞迁移和管形成,这表明针对血管生成的潜在治疗应用.
科学领域:
- 内皮细胞生物学 内皮细胞生物学
- 表观遗传学 在表观遗传学中,表观遗传学是指表观遗传学.
- 血管生成的分子机制
背景情况:
- 内皮细胞 (ECs) 对于心血管和全身功能至关重要.
- 蛋白质素化,由基氨酸脱胺酶 (PADs) 调节,影响基因表达.
- PADs在血管生成中的作用尚不清楚.
研究的目的:
- 研究PADs在内皮血管生成中的作用.
- 评估PAD抑制对EC功能的影响.
主要方法:
- 使用人类静脉 (HUVEC) 和微血管内皮细胞 (HMEC-1).
- 使用不可逆转的抑制剂 (BB-Cl-amidine,Cl-amidine,F-amidine) 抑制了PADs的活动.
- 分析了EC的扩散,迁移,毛细血管状管的形成,基因表达和信号.
主要成果:
- PAD抑制剂降低了组织素H3的素化 (H3cit).
- 抑制PADs降低了EC迁移和毛细血管样管的形成.
- PAD抑制增加了PEDF,降低了VEGF的表达,促进了血管静止活性.
结论:
- 药理上抑制素化显示出针对血管生成的前景.
- PAD抑制剂可以作为治疗剂来控制病理性血管生成.
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