| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 4346284 | Neuroscience Letters | 2010 | 5 Pages |
Confocal immunohistochemistry shows that neurotrophin-3 (NT-3) and its receptor tropomyosin-related tyrosin kinase C (trkC) are present in both neonatal (P6) and adult (P45) mouse motor nerve terminals in neuromuscular junctions (NMJ) colocalized with several synaptic proteins. NT-3 incubation (1–3 h, in the range 10–200 ng/ml) does not change the size of the evoked and spontaneous endplate potentials at P45. However, NT-3 (1 h, 100 ng/ml) strongly potentiates evoked ACh release from the weak (70%) and the strong (50%) axonal inputs on dually innervated postnatal endplates (P6) but not in the most developed postnatal singly innervated synapses at P6. The present results indicate that NT-3 has a role in the developmental mechanism that eliminates redundant synapses though it cannot modulate synaptic transmission locally as the NMJ matures.
