FURTHER-STUDIES ON MOTOR AND SENSORY NERVE REGENERATION IN MICE WITH DELAYED WALLERIAN DEGENERATION

Citation
Mc. Brown et al., FURTHER-STUDIES ON MOTOR AND SENSORY NERVE REGENERATION IN MICE WITH DELAYED WALLERIAN DEGENERATION, European journal of neuroscience, 6(3), 1994, pp. 420-428
Citations number
29
Categorie Soggetti
Neurosciences
ISSN journal
0953816X
Volume
6
Issue
3
Year of publication
1994
Pages
420 - 428
Database
ISI
SICI code
0953-816X(1994)6:3<420:FOMASN>2.0.ZU;2-X
Abstract
The axons of both peripheral and central neurons in C57BL/Wld(s) (C57B L/Ola) mice are unique among mammals in degenerating extremely slowly after axotomy. Motor and sensory axons attempting to regenerate are th us confronted with an intact distal nerve stump rather than axon- and myelin-free Schwann cell-filled endoneurial tubes. Surprisingly, howev er, motor axons in the sciatic nerve innervating the soleus muscle reg enerate rapidly , and there is evidence that they may use Schwann cell s associated with unmyelinated fibres as a pathway. If this is so, mot or axon regeneration might be impaired in C57BL/Wld(s) mice in the phr enic nerve, which has very few unmyelinated fibres. We found that as l ong as the myelinated axons in the distal stump of the phrenic nerve r emained intact (up to 10 days), regeneration of motor axons did not oc cur, in spite of vigorous production of sprouts at the crush site. In contrast to motor axons, myelinated sensory axons regenerate very poor ly in C57BL/Wld(s) mice, even in the presence of unmyelinated axons. W e showed that this was also due to adverse local conditions confrontin g nerve sprouts, for the dorsal root ganglion cell bodies responded no rmally to injury with a rapid induction of Jun protein-like immunoreac tivity and when the saphenous nerve was forced to degenerate more rapi dly by multiple crush lesions sensory axons regrew much more successfu lly. The findings show that motor and sensory axons in C57BL/Wld(s) mi ce, although very atypical in the way that they degenerate, are able t o regenerate normally but only in an appropriate environment. The resu lts also give support to the view that intact peripheral nerves either fail to encourage or actively inhibit axon growth, and that an unsuit able local environment can prevent regeneration even if the cell body is reacting normally to injury.