Protective effect of p53 on the viability of intervertebral disc nucleus pulposus cells under low glucose condition

Biochem Biophys Res Commun. 2017 Sep 2;490(4):1414-1419. doi: 10.1016/j.bbrc.2017.07.055. Epub 2017 Jul 11.

Abstract

P53 is a famous cancer suppressor and plays key roles in metabolism. Intervertebral disc (IVD) is the largest avascular cartilaginous structure in humans and its degeneration is a common cause of spine diseases initiated from damaged nucleus pulposus (NP) cells. The potential cause of disc degeneration has been attributed to aging, genetic factors, mechanical factors and nutrition. In this study, we found that p53 decreased and leaked to the cytoplasm in NP cells as the glucose level decreases, in contrast to cancer cells in which p53 increases and concentrates to the nuclei. Comparing with in p53 knockdown NP cells, relative high p53 expression in normal control NP cells inhibited autophagy and the pentose phosphate pathway. Furthermore, the expression of Sox 9 and type II collagen were higher in p53 normal control than p53 knockdown NP cells. Based on these results, we believe that relative high p53 facilitates NP cell viability and integrity.

Keywords: Intervertebral disc (IVD); Low glucose; Nucleus pulposus (NP) cells; p53.

MeSH terms

  • Autophagy / drug effects
  • Cell Line, Tumor
  • Cell Nucleus / genetics
  • Cell Nucleus / metabolism
  • Cell Survival / drug effects
  • Chondrocytes / cytology
  • Chondrocytes / drug effects*
  • Chondrocytes / metabolism
  • Collagen Type II / genetics
  • Collagen Type II / metabolism
  • Cytoplasm / drug effects
  • Cytoplasm / metabolism
  • Epithelial Cells / cytology
  • Epithelial Cells / drug effects
  • Epithelial Cells / metabolism
  • Gene Expression Regulation
  • Glucose / pharmacology*
  • Humans
  • Mesenchymal Stem Cells / cytology
  • Mesenchymal Stem Cells / drug effects*
  • Mesenchymal Stem Cells / metabolism
  • Nucleus Pulposus / cytology
  • Nucleus Pulposus / drug effects*
  • Nucleus Pulposus / metabolism
  • Pentose Phosphate Pathway / drug effects
  • Primary Cell Culture
  • RNA, Small Interfering / genetics
  • RNA, Small Interfering / metabolism
  • SOX9 Transcription Factor / genetics
  • SOX9 Transcription Factor / metabolism
  • Tumor Suppressor Protein p53 / antagonists & inhibitors
  • Tumor Suppressor Protein p53 / genetics*
  • Tumor Suppressor Protein p53 / metabolism

Substances

  • Collagen Type II
  • RNA, Small Interfering
  • SOX9 Transcription Factor
  • SOX9 protein, human
  • Tumor Suppressor Protein p53
  • Glucose