Effect of high concentration glucose and advanced glycation end products on MIP-1#alpha# mRNA expression in cultured human umbilical vein endothelial cells
Meng Xin, JIn Zhang, Difei Wang
Abstract
Meng Xin, JIn Zhang, Difei Wang
Abstract
To investigate the effect of high concentration glucose and advanced glycation end products (AGEs) on macrophage inflammatory protein-la (MlP-1#alpha#) mRNA expression in cultured human umbilical vein endothelial cells (HUVECs). HUVECs were cultured with AGEs alone at different concentrations (100, 200, or 400mg/L) for 24h and then co-cultured with 22mmol/L glucose and 400mg/L AGEs for 24h. The levels of MIP-l#alpha# mRNA expression in cultured HUVECs were detected by in situ hybridization. In situ hybridization showed that after exposure of HUVECs to AGEs alone at different concentrations (100, 200, 400mg/L) for 24h, the average integrated optical density values of MIP-1#alpha# mRNA expression in HUVECs were 18.76±3.17, 26.58±1.61 and 34.23 + 2.25 (BSA group, 13.83±1.24), with statistically significant differences between the groups (P<0.05). After exposure of HUVECs to 400mg/L AGEs and 22mmol/L glucose for 24h, the average integrated optical density values of MIP- 1#alpha# mRNA expression were 40.56±1.97, also with statistically significant differences between the groups (P<0.05). AGEs can promote the MIP-1#alpha# mRNA expression in cultured HUVECs in a dose-dependent manner, and there was a synergism between AGEs and high concentration glucose.
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To investigate the effect of high concentration glucose and advanced glycation end products (AGEs) on macrophage inflammatory protein-la (MlP-1#alpha#) mRNA expression in cultured human umbilical vein endothelial cells (HUVECs). HUVECs were cultured with AGEs alone at different concentrations (100, 200, or 400mg/L) for 24h and then co-cultured with 22mmol/L glucose and 400mg/L AGEs for 24h. The levels of MIP-l#alpha# mRNA expression in cultured HUVECs were detected by in situ hybridization. In situ hybridization showed that after exposure of HUVECs to AGEs alone at different concentrations (100, 200, 400mg/L) for 24h, the average integrated optical density values of MIP-1#alpha# mRNA expression in HUVECs were 18.76±3.17, 26.58±1.61 and 34.23 + 2.25 (BSA group, 13.83±1.24), with statistically significant differences between the groups (P<0.05). After exposure of HUVECs to 400mg/L AGEs and 22mmol/L glucose for 24h, the average integrated optical density values of MIP- 1#alpha# mRNA expression were 40.56±1.97, also with statistically significant differences between the groups (P<0.05). AGEs can promote the MIP-1#alpha# mRNA expression in cultured HUVECs in a dose-dependent manner, and there was a synergism between AGEs and high concentration glucose.
Key concepts: Umbilical vein, Glycation, Messenger RNA, In situ hybridization, Chemistry, Alpha (finance), Andrology, Molecular biology