Influence of acid and bile acid on ERK activity, PPARY expression and cell proliferation in normal h Influence of acid and bile acid on ERK activity, PPARY expression and cell proliferation in normal h

Influence of acid and bile acid on ERK activity, PPARY expression and cell proliferation in normal h

  • 期刊名字:世界胃肠病学杂志(英文版)
  • 文件大小:
  • 论文作者:Zhi-Ru Jiang,Jun Gong,Zhen-Ni
  • 作者单位:Department of Gastroenterology,Department of Anesthesiology,Department of Thoracic Surgery
  • 更新时间:2022-12-23
  • 下载次数:
论文简介

AIM: To observe the effects of acid and bile acid exposure on cell proliferation and the expression of extracellular signal-regulated protein kinase (ERK) and peroxisome proliferator-activated receptor Y (PPARy) in normal human esophageal epithelial cells in vitro.METHODS: In vitro cultured normal human esophageal epithelial cells were exposed to acidic media (pH 4.0-6.5), media containing different bile acid (250 μmol/L), media containing acid and bile acid, respectively.Cell proliferation was assessed using MTT and flow cytometry. The expressions of phosphorylated ERK1/2 and PPARy protein were determined by the immunoblotting technique.RESULTS: Acid-exposed (3 min) esophageal cells exhibited a significant increase in proliferation ratio,S phase of the cell cycle (P<0.05) and the level of phosphorylated ERK1/2 protein. When the acid-exposure period exceeded 6 min, we observed a decrease in proliferation ratio and S phase of the cell cycle, with an increased apoptosis ratio (P<0.05). Bile acid exposure (3-12 min) also produced an increase in proliferation ratio, S phase of the cell cycle (P<0.05)and phosphorylated ERK1/2 expression. On the contrary,deoxycholic acid (DCA) exposure (>20 min) decreased proliferation ratio. Compared with bile acid exposure (pH 7.4), bile acid exposure (pH 6.5, 4) significantly decreased proliferation ratio (P<0.05). There was no expression of PPARY in normal human esophageal epithelial cells.CONCLUSION: The rapid stimuli of acid or bile acid increase proliferation in normal human esophageal epithelial cells by activating the ERK pathway.

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