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Homocysteine induces vascular endothelial growth factor expression in differentiated THP-1 macrophages

机译:同型半胱氨酸诱导分化的THP-1巨噬细胞表达血管内皮生长因子

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Hyperhomocysteinemia has been reported to be an independent risk factor for atherosclerosis and atherothrombosis. However, the molecular mechanism by which hyperhomocysteinemia can lead to atherosclerosis and atherothrombosis has not been completely described. Vascular endothelial growth factor (VEGF) has been proposed to play an important role in the progression of atherosclerosis. In the present study, we hypothesized that hyperhomocysteinemia might be associated with VEGF expression in atherosclerotic lesions. We investigated VEGF mRNA expression and VEGF secretion by homocysteine (Hcy) in differentiated THP-1 macrophages. As a result, it has been revealed that VEGF mRNA was upregulated by Hcy in a dose- and time-dependent manner in THP-1 macrophages with the increase in VEGF secretion. Importantly, other sulfur compounds, such as methionine and cysteine, showed no effect on VEGF expression, indicating that homocysteine specifically induced VEGF. Our findings suggest that hyperhomocysteinemia could promote the development of atherosclerotic lesions through VEGF induction in macrophages.
机译:据报道,高同型半胱氨酸血症是动脉粥样硬化和动脉血栓形成的独立危险因素。然而,高同型半胱氨酸血症可导致动脉粥样硬化和动脉粥样硬化的分子机制尚未完全描述。已经提出血管内皮生长因子(VEGF)在动脉粥样硬化的进展中起重要作用。在本研究中,我们假设高同型半胱氨酸血症可能与动脉粥样硬化病变中的VEGF表达有关。我们调查了高分化的THP-1巨噬细胞中高半胱氨酸(Hcy)的VEGF mRNA表达和VEGF分泌。结果表明,在THP-1巨噬细胞中,Hcy以剂量和时间依赖性方式上调VEGF mRNA,这与VEGF分泌增加有关。重要的是,其他硫化合物,例如蛋氨酸和半胱氨酸,对VEGF表达无影响,表明同型半胱氨酸可特异性诱导VEGF。我们的发现表明高半胱氨酸血症可以通过巨噬细胞中的VEGF诱导促进动脉粥样硬化病变的发展。

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