4.7 Article

Adenosine 5′-triphosphate stimulates the increase of TGF-β1 in rat mesangial cells under high-glucose conditions via reactive oxygen species and ERK1/2

Journal

ACTA PHARMACOLOGICA SINICA
Volume 30, Issue 12, Pages 1601-1606

Publisher

ACTA PHARMACOLOGICA SINICA
DOI: 10.1038/aps.2009.155

Keywords

diabetic nephropathy; reactive oxygen species; adenosine 5'-triphosphate; extracellular signal-regulated kinase 1/2; transforming growth factor-beta 1; mesangial cells

Funding

  1. Shanghai Natural Science Foundation [09ZR1404200]
  2. National Natural Science Foundation of China [3047627]

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Aim: To investigate the role of adenosine 5'-triphosphate (ATP)-induced generation of reactive oxygen species (ROS) and phosphorylation of extracellular signal-regulated kinase 1/2 (ERK1/2) in the production of transforming growth factor-beta 1 (TGF-beta 1) in cultured rat glomerular mesangial cells under high-glucose conditions. Methods: Subconfluent glomerular mesangial cells were serum-starved for 24 h and pretreated with suramin, diphenylenechloride iodonium (DPI) or PD98059 followed by stimulation with a high concentration of glucose (30 mmol/L D-glucose) or ATP (300 mu mol/L). Extracellular and total ATP and ROS production were detected using commercially available kits. Phosphorylation of ERK1/2 was evaluated by Western blot. TGF-beta 1 mRNA expression was examined by real-time PCR. Results: Suramin had a dose-dependent inhibitory effect on the generation of ROS induced by high glucose. Extracellular ATP production by mesangial cells increased markedly after a 2-h incubation with high glucose. ROS production was upregulated in mesangial cells after 5 min incubation with 300 mu mol/L ATP and was sustained for 120 min. ERK1/2 was significantly activated after 5 min incubation of mesangial cells with ATP, this activation was partially inhibited by DPI. The effects of high glucose on TGF-beta 1 mRNA were markedly inhibited by suramin, DPI or PD98059. Conclusion: Our results suggest that a high concentration of glucose increases the extracellular levels of ATP in mesangial cells within a short time-frame. ATP, in turn, activates ERK1/2, an effect which is at least partially dependent on ROS, which results in the upregulation of TGF-beta 1.

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