Résumé
The aim of this study was to approach the question of neuronal dependence on neurotrophins during embryonic development in mice in a way other than gene targeting. We employed amyogenic mouse embryos and fetuses that develop without any skeletal myoblasts or skeletal muscle and consequently lose motor and proprioceptive neurons. We hypothesized that if, in spite of the complete inability to maintain motor and proprioceptive neurons, the remaining spinal and dorsal root ganglia tissues of amyogenic fetuses still contain any of the neurotrophins, that particular neurotrophin alone is not sufficient for the maintenance of motor and proprioceptive neurons. Moreover, if the remaining spinal and dorsal root ganglia tissues still contain any of the neurotrophins, that particular neurotrophin alone may be sufficient for the maintenance of the remaining neurons (i.e., mostly non-muscle- and a few muscle-innervating neurons). To test the role of the spinal cord and dorsal root ganglia tissues in the maintenance of its neurons, we performed immunohistochemistry employing double-mutant and control tissues and antibodies against neurotrophins and their receptors. Our data suggested that: (a) during the peak of motor neuron cell death, the spinal cord and dorsal root ganglia distribution of neurotrophins was not altered; (b) the distribution of BDNF, NT-4/5, TrkB and TrkC, and not NT-3, was necessary for the maintenance of the spinal cord motor neurons; (c) the distribution of BDNF, NT-4/5 and TrkC, and not NT-3 and Trk B, was necessary for the maintenance of the DRG proprioceptive neurons; (d) NT-3 was responsible for the maintenance of the remaining neurons and glia in the spinal cord and dorsal root ganglia (possibly via TrkB).
Langue d'origine | English |
---|---|
Pages (de-à) | 613-620 |
Nombre de pages | 8 |
Journal | International Journal of Developmental Neuroscience |
Volume | 23 |
Numéro de publication | 7 |
DOI | |
Statut de publication | Published - nov. 2005 |
Note bibliographique
Funding Information:This work was supported by a Canadian Institutes of Health Research (CIHR) and the Hospital for Sick Children Foundation (HSCF) research grant and infrastructure grants from Canada Foundation for Innovation (CFI) and Dalhousie Medical research Foundation (DMRF) to B.K.
ASJC Scopus Subject Areas
- Developmental Neuroscience
- Developmental Biology