1. Academic Validation
  2. Lipopolysaccharide downregulates the expression of p53 through activation of MDM2 and enhances activation of nuclear factor-kappa B

Lipopolysaccharide downregulates the expression of p53 through activation of MDM2 and enhances activation of nuclear factor-kappa B

  • Immunobiology. 2015 Jan;220(1):136-41. doi: 10.1016/j.imbio.2014.08.010.
Erdenezaya Odkhuu 1 Adilsaikhan Mendjargal 2 Naoki Koide 3 Yoshikazu Naiki 3 Takayuki Komatsu 3 Takashi Yokochi 3
Affiliations

Affiliations

  • 1 Department of Microbiology and Immunology, Aichi Medical University School of Medicine, Nagakute, Aichi 480-1195, Japan; Departments of Anatomy, Mongolian National University of Medical Sciences, Ulaanbaatar 210648, Mongolia. Electronic address: zayamgl@aichi-med-u.ac.jp.
  • 2 Oncology, Mongolian National University of Medical Sciences, Ulaanbaatar 210648, Mongolia.
  • 3 Department of Microbiology and Immunology, Aichi Medical University School of Medicine, Nagakute, Aichi 480-1195, Japan.
Abstract

The effect of lipopolysaccharide (LPS) on the expression of p53 protein in RAW 264.7 macrophage cells was examined. LPS downregulated the expression of p53 protein 4-24 h after the stimulation. LPS-induced p53 inhibition was restored with pharmacological inhibitors of c-jun N-terminal kinase (JNK) and phosphatidylinositol 3-kinase (PI3K). It was also restored by inhibitors of MDM2 activation and Proteasome. LPS-induced p53 inhibition corresponded to activation of MDM2. LPS-induced MDM2 activation was prevented by inhibitors of JNK and PI3K. The expression of p65 NF-κB at a late stage after LPS stimulation was downregulated in the presence of a MDM2 Inhibitor. Nutlin-3 as a MDM2 Inhibitor reduced LPS-induced production of nitric oxide but not tumor necrosis factor-α. Administration of LPS into mice downregulated the in vivo expression of p53 in the livers. Taken together, LPS was suggested to downregulate the expression of p53 via activation of MDM2 and enhance the activation of NF-κB at a late stage.

Keywords

Lipopolysaccharide; MDM2; NF-κB; Nutlin-3; P53.

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