Morphology and nanomechanics of sensory neurons growth cones following peripheral nerve injury

PLoS One. 2013;8(2):e56286. doi: 10.1371/journal.pone.0056286. Epub 2013 Feb 13.

Abstract

A prior peripheral nerve injury in vivo, promotes a rapid elongated mode of sensory neurons neurite regrowth in vitro. This in vitro model of conditioned axotomy allows analysis of the cellular and molecular mechanisms leading to an improved neurite re-growth. Our differential interference contrast microscopy and immunocytochemistry results show that conditioned axotomy, induced by sciatic nerve injury, did not increase somatic size of adult lumbar sensory neurons from mice dorsal root ganglia sensory neurons but promoted the appearance of larger neurites and growth cones. Using atomic force microscopy on live neurons, we investigated whether membrane mechanical properties of growth cones of axotomized neurons were modified following sciatic nerve injury. Our data revealed that neurons having a regenerative growth were characterized by softer growth cones, compared to control neurons. The increase of the growth cone membrane elasticity suggests a modification in the ratio and the inner framework of the main structural proteins.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / metabolism
  • Animals
  • Axotomy / methods
  • Biomechanical Phenomena
  • Cells, Cultured
  • Elasticity
  • Female
  • Ganglia, Spinal / cytology
  • Ganglia, Spinal / metabolism
  • Ganglia, Spinal / physiology*
  • Growth Cones / metabolism
  • Growth Cones / physiology*
  • Immunohistochemistry
  • Mice
  • Microscopy, Atomic Force
  • Microscopy, Phase-Contrast
  • Nerve Regeneration / physiology
  • Peripheral Nerve Injuries / physiopathology*
  • Sciatic Nerve / injuries
  • Sensory Receptor Cells / metabolism
  • Sensory Receptor Cells / physiology*
  • Tubulin / metabolism

Substances

  • Actins
  • Tubulin
  • beta3 tubulin, mouse

Grants and funding

This work was supported by the COST- EU Action on “Applications of Atomic Force Microscopy to NanoMedecine and Life Sciences” (TD1002- AFM4NanoMed&Bio) and by the Association française contre les myopathies (AFM). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.