Effects of long-term low oxygen tension in human chondrosarcoma cells

J Cell Biochem. 2018 Feb;119(2):2320-2332. doi: 10.1002/jcb.26394. Epub 2017 Oct 18.

Abstract

The cell-based therapies could be potential methods to treat damaged cartilage tissues. Instead of native hyaline cartilage, the current therapies generate mainly weaker fibrocartilage-type of repair tissue. A correct microenvironment influences the cellular phenotype, and together with external factors it can be used, for example, to aid the differentiation of mesenchymal stem cells to defined types of differentiated adult cells. In this study, we investigated the effect of long-term exposure to 5% low oxygen atmosphere on human chondrosarcoma HCS-2/8 cells. This atmosphere is close to normal oxygen tension of cartilage tissue. The proteome was analyzed with label-free mass spectrometric method and further bioinformatic analysis. The qRT-PCR method was used to gene expression analysis, and ELISA and dimethylmethylene blue assays for type II collagen and sulfated glycosaminoglycan measurements. The 5% oxygen atmosphere did not influence cell proliferation, but enhanced slightly ACAN and COL2A1 gene expression. Proteomic screening revealed a number of low oxygen-induced protein level responses. Increased ones included NDUFA4L2, P4HA1, NDRG1, MIF, LDHA, PYGL, while TXNRD1, BAG2, TXN2, AQSTM1, TNFRSF1B, and EPHX1 decreased during the long-term low oxygen atmosphere. Also a number of proteins previously not related to low oxygen tension changed during the treatment. Of those S100P, RPSS26, NDUFB11, CDV3, and TUBB8 had elevated levels, while ALCAM, HLA-B, EIF1, and ACOT9 were lower in the samples cultured at low oxygen tension. In conclusion, low oxygen condition causes changes in the cellular amounts of several proteins.

Keywords: S100 proteins; chondrosarcoma; extracellular matrix; hypoxia, label-free quantitative proteomics.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aggrecans / metabolism
  • Bone Neoplasms / metabolism*
  • Cell Culture Techniques / methods
  • Cell Differentiation / drug effects
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Chondrosarcoma / metabolism*
  • Collagen Type II / metabolism
  • Gene Expression Regulation / drug effects
  • Humans
  • Mass Spectrometry
  • Oxygen / pharmacology*
  • Phenotype
  • Proteome / drug effects*
  • Proteomics / methods*

Substances

  • ACAN protein, human
  • Aggrecans
  • COL2A1 protein, human
  • Collagen Type II
  • Proteome
  • Oxygen