Abstract

IntroductionDevelopment of cell therapies for repairing the intervertebral disc is limited by the lack of a source of healthy human disc cells. Stem cells, particularly mesenchymal stem cells, are seen as a potential source but differentiation strategies are limited by the lack of specific markers that can distinguish disc cells from articular chondrocytes.MethodsWe searched for markers using the differential in-gel electrophoresis proteomic technology to compare proteins of bovine nucleus pulposus cells, phenotypically similar to mature human nucleus cells, with those of bovine articular chondrocytes. In the cohort of the differentially expressed proteins identified by mass spectrometry, cytokeratin 8 (CK8) was further validated by immunostaining of freshly isolated cells and frozen tissue sections using monoclonal antibodies.ResultsWe identified a set of 14 differentially expressed proteins. Immunohistochemistry showed that only a subset of cells (approximately 10%) was positive for one of these proteins, CK8, an intermediate filament protein present in epithelial but not mesenchymal cells. In tissue sections, CK8-positive cells were seen in all discs examined and appeared as small isolated clusters surrounded by gelatinous matrix. Notochordal nucleus pulposus cells from pig, phenotypically similar to human infant nucleus pulposus cells, were all CK8-positive. The mesenchymal intermediate filament protein vimentin was present in all bovine and porcine nucleus pulposus cells.ConclusionsThe notochordal cell population is reported to disappear from the nucleus pulposus of bovine discs before birth and from human discs in childhood. However our finding of the co-expression of vimentin and CK8 in small isolated clusters of the bovine nucleus pulposus cells indicates that a subpopulation of notochordal-like cells remains in the mature bovine disc. This finding agrees with reports in the literature on co-expression of cytokeratins and vimentin in adult human discs. As notochordal cells produce factors that promote matrix production, the CK8-positive subpopulation could have important implications for activity and survival of the nucleus pulposus, and should be considered in development of cell therapies for disc repair. In addition, the finding of differential expression of proteins in the cell population of nucleus pulposus has implications with regard to the search for specific markers.

Highlights

  • Development of cell therapies for repairing the intervertebral disc is limited by the lack of a source of healthy human disc cells

  • Notochordal cells were obtained from the pig nucleus pulposus (NP) by a 1-hour digestion in 0.025% protease serum-free Dulbecco's modified Eagle's medium (DMEM) followed by an overnight digestion with 0.0125% type I collagenase in DMEM supplemented with 10% fetal bovine serum (Invitrogen Corporation) in accordance with the protocol described by Guehring and colleagues [28]

  • Two-dimensional proteome map of freshly isolated bovine nucleus pulposus cells To identify specific markers of freshly isolated bovine NP cells, the Cy3- and Cy5-labelled water-soluble protein fractions of NP cells and articular chondrocyte (AC) were resolved by 2D gel electrophoresis

Read more

Summary

Introduction

Development of cell therapies for repairing the intervertebral disc is limited by the lack of a source of healthy human disc cells. Low back pain constitutes a major health problem and a huge economic burden [1] It is highly associated with degeneration of the intervertebral disc [2]. Treatments on offer are still mainly palliative or surgical and do not improve the ability of the disc to regain its original architecture and function. Biological approaches, those that aim to produce a tissue-engineered disc or to insert cells into the damaged NP to regenerate the matrix and restore the disc's biomechanical function, are seen as a potential alternative [5].

Methods
Results
Discussion
Conclusion

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.