[Biology and mechanobiology of the intervertebral disc]

Neurocirugia (Astur). 2017 May-Jun;28(3):135-140. doi: 10.1016/j.neucir.2016.12.002. Epub 2017 Jan 24.
[Article in Spanish]

Abstract

The intervertebral disc (IVD) is noted for its low cell content, and being the largest avascular structure of human body. The low amount of cells in the disc have to adapt to an anaerobic metabolism with low oxygen pressure and acidic pH. Apart from surviving in an adverse microenvironment, they are exposed to a high level of mechanical stress. The biological adaptation of cells to acidosis and hyperosmolarity conditions are regulated by mechanoproteins, which are responsible for converting a mechanical signal into a cellular response, thus modifying its gene expression. Mechanobiology helps us to better understand the pathophysiology of IVD and its potential biological repair.

Keywords: Biología del disco intervertebral; Disco intervertebral; Intervertebral disc; Intervertebral disc biology; Intervertebral disc mechanobiology; Mecanobiología del disco intervertebral; Mecanoproteínas en el disco intervertebral; Mechanoproteins in the intervertebral disc.

Publication types

  • Review

MeSH terms

  • Cell Hypoxia
  • Cellular Microenvironment
  • Chondrocytes / physiology
  • Energy Metabolism
  • Extracellular Matrix Proteins / biosynthesis
  • Extracellular Matrix Proteins / genetics
  • Fibroblasts / physiology
  • Gene Expression Regulation
  • Humans
  • Hydrogen-Ion Concentration
  • Intervertebral Disc / anatomy & histology
  • Intervertebral Disc / blood supply
  • Intervertebral Disc / cytology
  • Intervertebral Disc / physiology*
  • Intervertebral Disc Displacement / metabolism
  • Intervertebral Disc Displacement / pathology
  • Mechanotransduction, Cellular / physiology
  • Metalloproteases / biosynthesis
  • Metalloproteases / genetics
  • Osmolar Concentration
  • Proteoglycans / biosynthesis
  • Proteoglycans / genetics
  • Stress, Mechanical

Substances

  • Extracellular Matrix Proteins
  • Proteoglycans
  • Metalloproteases