Dulak Józef, Tomala Katarzyna, Loboda Agnieszka, Józkowicz Alicja
Department of Cell Biochemistry, Faculty of Biotechnology, Jagiellonian University, Gronostajowa 7, 30-387 Kraków, Poland.
Life Sci. 2004 Oct 8;75(21):2573-86. doi: 10.1016/j.lfs.2004.05.021.
Synthesis of vascular endothelial growth factor (VEGF), the major angiogenic molecule, is induced by nitric oxide (NO) in various cell types, including vascular smooth muscle cells (VSMC). Therefore, compounds which inhibit NO generation can also influence VEGF synthesis. Here we investigated the effect of increased glucose concentration (25 mM vs. 5.5 mM) on cytokine-induced VEGF synthesis in rat VSMC. The cells growing in the medium containing 5.5 mM glucose and exposed to IL-1-beta, TNF-alpha and IFN-gamma induced expression of an inducible isoform of nitric oxide synthase (NOS II). This is followed by generation of NO and the concomitant expression of VEGF gene and release of VEGF protein. In contrast, 25 mM glucose impaired induction of NOS II expression and thus NO synthesis was lower than in 5.5 mM glucose. Consequently, the VEGF promoter activation was attenuated, resulting in decreased mRNA synthesis and lower production of VEGF protein. The results indicate that abnormally high concentrations of glucose can impair generation of NO and the NO-dependent VEGF synthesis. This may play a role in the development and progression of vascular dysfunctions in cardiovascular diseases.
血管内皮生长因子(VEGF)是主要的血管生成分子,在包括血管平滑肌细胞(VSMC)在内的多种细胞类型中,一氧化氮(NO)可诱导其合成。因此,抑制NO生成的化合物也会影响VEGF的合成。在此,我们研究了高糖浓度(25 mM与5.5 mM相比)对大鼠VSMC中细胞因子诱导的VEGF合成的影响。在含有5.5 mM葡萄糖的培养基中生长并暴露于白细胞介素-1β(IL-1-β)、肿瘤坏死因子-α(TNF-α)和干扰素-γ(IFN-γ)的细胞,可诱导一氧化氮合酶(NOS II)诱导型同工型的表达。随后产生NO,并伴随VEGF基因的表达和VEGF蛋白的释放。相比之下,25 mM葡萄糖会损害NOS II表达的诱导,因此NO合成低于5.5 mM葡萄糖时的水平。结果,VEGF启动子的激活减弱,导致mRNA合成减少和VEGF蛋白产生降低。这些结果表明,异常高浓度的葡萄糖会损害NO的生成以及NO依赖的VEGF合成。这可能在心血管疾病中血管功能障碍的发生和发展中起作用。