Potential of co-culture of nucleus pulposus mesenchymal stem cells and nucleus pulposus cells in hyperosmotic microenvironment for intervertebral disc regeneration

Cell Biol Int. 2013 Aug;37(8):826-34. doi: 10.1002/cbin.10110. Epub 2013 Apr 18.

Abstract

Nucleus pulposus mesenchymal stem cells (NPMSCs) are a potential cell source for intervertebral disc (IVD) regeneration, but little is known about their response to IVD-like high osmolarity (400 mOsm). This study was to investigate the viability, proliferation and protein biosynthesis of nucleus pulposus cells (NPCs), NPMSCs and co-cultured NPMSCs-NPCs under IVD-like high osmolarity conditions. NPCs and NPMSCs were isolated and cultured under standard and IVD-like high osmolarity conditions for 1 or 2 weeks. Cell viability was measured by annexin V-FITC and PI staining, and cell proliferation measured by MTT assay. The expression of SOX-9, aggrecan and collagen-II was measured by RT-PCR and Western blot analyses. IVD-like high osmolarity condition slightly inhibited cell viability and decreased the expression of SOX-9, aggrecan and collagen-II at the mRNA and protein levels in all groups compared with standard condition. NPMSCs could tolerate IVD-like high osmolarity, and NPCs-NPMSCs co-culture increased cell proliferation and the expression of SOX-9, aggrecan and collagen-II under both culture conditions, suggesting that co-culture of NPMSCs-NPCs has potential application for IVD regeneration.

Keywords: co-culture; intervertebral disc; mesenchymal stem cell; nucleus pulposus; osmolarity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aggrecans / genetics
  • Aggrecans / metabolism
  • Animals
  • Cell Differentiation
  • Cell Proliferation
  • Cell Survival
  • Cells, Cultured
  • Coculture Techniques
  • Collagen Type II / genetics
  • Collagen Type II / metabolism
  • Gene Expression
  • Intervertebral Disc / pathology
  • Intervertebral Disc / physiology*
  • Intervertebral Disc Degeneration / pathology
  • Intervertebral Disc Degeneration / therapy
  • Male
  • Mesenchymal Stem Cells / physiology*
  • Osmolar Concentration
  • Protein Biosynthesis
  • Rats
  • Rats, Sprague-Dawley
  • Regeneration*
  • Regenerative Medicine
  • SOX9 Transcription Factor / genetics
  • SOX9 Transcription Factor / metabolism

Substances

  • Aggrecans
  • Collagen Type II
  • SOX9 Transcription Factor