Proteomic analysis of bone tissues of patients with osteonecrosis of the femoral head

OMICS. 2009 Dec;13(6):453-66. doi: 10.1089/omi.2009.0057.

Abstract

Osteonecrosis of the femoral head (ONFH) is a devastating disease that can result in a femoral head collapse. By proteomics analysis, we identified 1,967 proteins with two or more unique peptides from ONFH and from control bones with a false discovery rate of 4.8%. Using spectral counting, we identified 141 overexpressed and 56 underexpressed proteins comparing ONFH bones to the controls. GSEA (gene set enrichment analysis) revealed that proteins overexpressed in ONFH are enriched for gene sets related to multiple myeloma and adult T-cell lymphoma (ATL), and to JAK2-dependent genes. We confirmed the underexpression of CHST2 (isoform 1 of carbohydrate sulfotransferase 2), a key protein involved in biosynthesis of chondroitin sulfate proteoglycans, and the underexpression of GPCR26 (G-protein coupled receptor 26), a protein that mediates intracellular calcium mobilization, in ONFH bones compared to controls. Taken together, our data suggest that biosynthesis of chondroitin sulfate proteoglycans and cation transport and mobilization may be a key process involved in the pathogenesis of ONFH. Our analysis sheds new light on the understanding of the pathogenesis of ONFH.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Bone and Bones / chemistry*
  • Bone and Bones / metabolism
  • Carbohydrate Sulfotransferases
  • Chromatography, Liquid / methods
  • Female
  • Femur Head Necrosis* / metabolism
  • Femur Head Necrosis* / pathology
  • Femur Head Necrosis* / physiopathology
  • Femur Head* / chemistry
  • Femur Head* / metabolism
  • Femur Head* / pathology
  • Humans
  • Male
  • Middle Aged
  • Molecular Sequence Data
  • Protein Isoforms / metabolism
  • Proteome / analysis*
  • Proteomics / methods
  • Receptors, G-Protein-Coupled / metabolism
  • Sulfotransferases / metabolism
  • Tandem Mass Spectrometry / methods

Substances

  • Protein Isoforms
  • Proteome
  • Receptors, G-Protein-Coupled
  • Sulfotransferases