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Substratum preferences of motor and sensory neurons in postnatal and adult rats
Author(s) -
GonzalezPerez Francisco,
Alé Albert,
Santos Daniel,
Barwig Christina,
Freier Thomas,
Navarro Xavier,
Udina Esther
Publication year - 2016
Publication title -
european journal of neuroscience
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.346
H-Index - 206
eISSN - 1460-9568
pISSN - 0953-816X
DOI - 10.1111/ejn.13057
Subject(s) - neurite , laminin , fibronectin , neuroscience , sensory system , reinnervation , spinal cord , neurofilament , biology , extracellular matrix , axon , sciatic nerve , anatomy , microbiology and biotechnology , immunology , immunohistochemistry , in vitro , biochemistry
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 (~50%) or fibronectin (~35%), whereas motoneurons extended longer neurites (~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 in vivo , 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 1 month 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 α5β1 (receptor for fibronectin) and α7β1 integrin (receptor for laminin) in spinal cord and DRG 2 days after injury. Postnatal animals showed a higher increase of α5β1 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.