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      Differential Response of Bovine Mature Nucleus Pulposus and Notochordal Cells to Hydrostatic Pressure and Glucose Restriction

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          Abstract

          Objective

          The nucleus pulposus of the human intervertebral disc contains 2 cell types: notochordal (NC) and mature nucleus pulposus (MNP) cells. NC cell loss is associated with disc degeneration and this process may be initiated by mechanical stress and/or nutrient deprivation. This study aimed to investigate the functional responses of NC and MNP cells to hydrostatic pressures and glucose restriction.

          Design

          Bovine MNP and NC cells were cultured in 3-dimensional alginate beads under low (0.4-0.8 MPa) and high (1.6-2.4 MPa) dynamic pressure for 24 hours. Cells were cultured in either physiological (5.5 mM) glucose media or glucose-restriction (0.55 mM) media. Finally, the combined effect of glucose restriction and high pressure was examined.

          Results

          Cell viability and notochordal phenotypic markers were not significantly altered in response to pressure or glucose restriction. MNP cells responded to low pressure with an increase in glycosaminoglycan (GAG) production while high pressure significantly decreased ACAN gene expression compared with atmospheric controls. NC cells showed no response in matrix gene expression or GAG production with either loading regime. Glucose restriction decreased NC cell TIMP-1 expression but had no effect on MNP cells. The combination of glucose restriction and high pressure only affected MNP cell gene expression, with decreased ACAN, Col2α1, and ADAMTS-5 expression.

          Conclusion

          This study shows that NC cells are more resistant to acute mechanical stresses than MNP cells and provides a strong rationale for future studies to further our understanding the role of NC cells within the disc, and the effects of long-term exposure to physical stresses.

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          Author and article information

          Journal
          Cartilage
          Cartilage
          CAR
          spcar
          Cartilage
          SAGE Publications (Sage CA: Los Angeles, CA )
          1947-6035
          1947-6043
          29 May 2018
          April 2020
          : 11
          : 2 , Special Issue: Spine
          : 221-233
          Affiliations
          [1 ]Department of Anatomy and Medical Imaging, Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand
          [2 ]Department of Chemical and Materials Engineering, Faculty of Engineering, University of Auckland, Auckland, New Zealand
          Author notes
          [*]Susan Read McGlashan, Department of Anatomy and Medical Imaging, School of Medical Sciences, University of Auckland, 85 Park Road, Private Bag 92019, Auckland 1023, New Zealand. Email: s.mcglashan@ 123456auckland.ac.nz
          Author information
          https://orcid.org/0000-0002-8666-2456
          Article
          PMC7097982 PMC7097982 7097982 10.1177_1947603518775795
          10.1177/1947603518775795
          7097982
          29808709
          9366855c-7343-4e82-bcb5-8833b9bb32a0
          © The Author(s) 2018
          History
          Funding
          Funded by: Auckland Medical Research Foundation, FundRef https://doi.org/10.13039/501100001511;
          Award ID: 3626882
          Categories
          Basic Science Papers
          Different Cells for Spinal Tissue Engineering
          Custom metadata
          ts1

          extracellular matrix,alginate culture,notochordal cells,glucose,hydrostatic pressure

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