4.5 Article

Substratum preferences of motor and sensory neurons in postnatal and adult rats

Journal

EUROPEAN JOURNAL OF NEUROSCIENCE
Volume 43, Issue 3, Pages 431-442

Publisher

WILEY
DOI: 10.1111/ejn.13057

Keywords

chitosan; extracellular matrix; neurite outgrowth; peripheral nerve; regeneration

Categories

Funding

  1. European Community [278612]

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After peripheral nerve injuries, damaged axons can regenerate but functional recovery is limited by the specific reinnervation of targets. In this study we evaluated if motor and sensory neurites have a substrate preference for laminin and fibronectin in postnatal and adult stages. In postnatal dorsal root ganglia (DRG) explants, sensory neurons extended longer neurites on collagen matrices enriched with laminin (similar to 50%) or fibronectin (similar to 35%), whereas motoneurons extended longer neurites (similar to 100%) in organotypic spinal cord slices embedded in fibronectin-enriched matrix. An increased percentage of parvalbumin-positive neurites (presumptive proprioceptive) vs. neurofilament-positive neurites was also found in DRG in fibronectin-enriched matrix. To test if the different preference of neurons for extracellular matrix components was maintained invivo, these matrices were used to fill a chitosan guide to repair a 6-mm gap in the sciatic nerve of adult rats. However, the number of regenerating motor and sensory neurons after 1month was similar between groups. Moreover, none of the retrotraced sensory neurons in DRG was positive for parvalbumin, suggesting that presumptive proprioceptive neurons had poor regenerative capabilities compared with other peripheral neurons. Using real-time PCR we evaluated the expression of 51 (receptor for fibronectin) and 71 integrin (receptor for laminin) in spinal cord and DRG 2days after injury. Postnatal animals showed a higher increase of 51 integrin, whereas both integrins were similarly expressed in adult neurons. Therefore, we conclude that motor and sensory axons have a different substrate preference at early postnatal stages but this difference is lost in the adult.

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