Muscle-derived neurotrophin-4 as an activity-dependent trophic signal for adult motor neurons.

@article{Funakoshi1995MusclederivedNA,
  title={Muscle-derived neurotrophin-4 as an activity-dependent trophic signal for adult motor neurons.},
  author={Hiroshi Funakoshi and Natale Belluardo and Ernest Arenas and Y. Yamamoto and Antonino Casabona and H{\aa}kan Persson and Carlos F. Ib{\'a}{\~n}ez},
  journal={Science},
  year={1995},
  volume={268 5216},
  pages={
          1495-9
        }
}
The production of neurotrophin-4 (NT-4) in rat skeletal muscle was found to depend on muscle activity. The amounts of NT-4 messenger RNA present decreased after blockade of neuromuscular transmission with alpha-bungarotoxin and increased during postnatal development and after electrical stimulation in a dose-dependent manner. NT-4 immunoreactivity was detected in slow, type I muscle fibers. Intramuscular administration of NT-4 induced sprouting of intact adult motor nerves. Thus, muscle-derived… 
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Neurotrophin 4/5 is required for the normal development of the slow muscle fiber phenotype in the rat soleus
TLDR
The developmental upregulation of NT-4/5 mRNA in rat SOL muscle fibers occurred earlier than theUpregulation of MyHC I/b mRNA associated with muscle fiber transformation, consistent with the idea that NT- 4/5 is involved in early events that lead to the up regulation of the slow MyHC isoform in this muscle.
Localized Synaptic Actions of Neurotrophin-4
TLDR
It is demonstrated that presynaptic potentiation is restricted to synapses on myocytes overexpressing NT-4 without affecting nearby synapses formed by the same neuron on control myocytes, suggesting activity-dependent secretion of neurotrophins can result in highly localized modification of neuronal connections.
Activity-Dependent Expression of NT-3 in Muscle Cells in Culture: Implications in the Development of Neuromuscular Junctions
TLDR
Activity-dependent expression of muscle NT-3 may contribute to the development of the neuromuscular synapse, and factor(s) induced by membrane depolarization appeared to enhance synaptic transmission at the developing neuromoscular junction.
Exercise-dependent regulation of glial cell line-derived neurotrophic factor (GDNF) expression in skeletal muscle and its importance for the neuromuscular system
TLDR
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The mRNA expression of neurotrophins in different skeletal muscles of young rats.
TLDR
Investigating the mRNA expressions of BDNF and NT-3 in three different skeletal muscles in 4- to 8- week-old rats using the reverse transcriptional polymerase chain reaction (RT-PCR) method found that there is a possibility that the different expression patterns of neurotrophins in muscles may be involved in the maturation of neuromuscular function in different muscles during the young developmental period.
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References

SHOWING 1-10 OF 55 REFERENCES
Neurotrophin 4/5 is a trophic factor for mammalian facial motor neurons.
TLDR
It is demonstrated that NT-4/5 also prevents injury-induced death of facial motor neurons in neonatal rats and may serve as therapeutic agents for motor neuron disease.
Neurotrophin-4 is a target-derived neurotrophic factor for neurons of the trigeminal ganglion.
TLDR
It is proposed that NT-4, together with the other three neurotrophins, orchestrate the innervation of the different structures of the developing whisker pad by the trigeminal ganglion, acting as target-derived neurotrophic factors for different subpopulations of trigemINAL ganglions neurons.
Brain-derived neurotrophic factor prevents the death of motoneurons in newborn rats after nerve section
TLDR
It is reported here that brain-derived neurotrophic factor can prevent the death of axotomized motoneurons in newborn rats, suggesting a role for this neurotrophin for motoneuron survival in vivo.
Differential expression of mRNAs for neurotrophins and their receptors after axotomy of the sciatic nerve
TLDR
Results show that expression of mRNAs for neurotrophins and their Trk receptors is differentially regulated after a peripheral nerve injury and a model is presented for how the different neurotrophin could cooperate to promote regeneration of injured peripheral nerves.
Neurotrophins promote motor neuron survival and are present in embryonic limb bud
TLDR
It is shown that picomolar concentrations of three neurotrophins, brain-derived neurotrophic factor, neurotroph in-3 and neurotrophin-5, can prevent the death of cultured embryonic rat spinal motor neurons and may be physiological motor neuron growth factors.
Widespread and Developmentally Regulated Expression of Neurotrophin‐4 mRNA in Rat Brain and Peripheral Tissues
TLDR
The peak of NT‐4 mRNA expression in several of the peripheral tissues coincided with the peak of naturally occurring neuronal cell death in peripheral ganglia, consistent with the possibility thatNT‐4 acts as a target‐derived trophic factor in vivo.
Role of muscle insulin-like growth factors in nerve sprouting: suppression of terminal sprouting in paralyzed muscle by IGF-binding protein 4
TLDR
In in vivo experiments, it is shown that local delivery of IGF-BP4 to Botulinum toxin A-paralyzed skeletal muscle effectively prevents nerve sprouting in that muscle, indicating that muscle IGFs play an essential role in intramuscular nerve sprouts.
Induction of motor neuron sprouting in vivo by ciliary neurotrophic factor and basic fibroblast growth factor
TLDR
The sprouting stimulus delivered by the factors showed limited penetrance into the muscle and restricted lateral spread from the injection site, and the effect of CNTF was potentiated twofold by coadministration of bFGF at doses of 2-20 ng daily, whereas treatment with bF GF alone failed to induce sprouting from either end plates or nodes of Ranvier.
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