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BDNF and NT4/5 promote survival and neurite outgrowth of pontocerebellar mossy fiber neurons

  • Sylvia A. Rabacchi
  • , Barbara Kruk
  • , Jason Hamilton
  • , Catrina Carney
  • , John R. Hoffman
  • , Sheryl L. Meyer
  • , Joe E. Springer
  • , Douglas H. Baird

Producción científica: Articlerevisión exhaustiva

41 Citas (Scopus)

Resumen

The neurotrophins nerve growth factor (NGF), brain-derived neurotrophic factor (BDNF), neurotrophin-3 (NT3), and NT4/5 are all found in the developing cerebellum. Granule cells, the major target neurons of mossy fibers, express BDNF during mossy fiber synaptogenesis. To determine whether neurotrophins contribute to the development of cerebellar afferent axons, we characterized the effects of neurotrophins on the growth of mossy fiber neurons from mice and rats in vitro. For a mossy fiber source, we used the basilar pontine nuclei (BPN), the major source of cerebellar mossy fibers in mammals. BDNF and NT4/5 increased BPN neuron survival, neurite outgrowth, growth cone size, and elongation rate, while neither NT3 nor NGF increased survival or outgrowth. In addition, BDNF and NT4/5 reduced the size of neurite bundles. Consistent with these effects, in situ hybridization on cultured basilar pontine neurons revealed the presence of mRNA encoding the TrkB receptor which binds both BDNF and NT4/5 with high affinity. We detected little or no message encoding the TrkC receptor which preferentially binds NT3. BDNF and NT4/5 also increased TrkB mRNA levels in BPN neurons. In addition to previously established functions as an autocrine/paracrine trophic factor for granule cells, the present results indicate that cerebellar BDNF may also act as a target-derived trophic factor for basilar pontine mossy fibers.

Idioma originalEnglish
Páginas (desde-hasta)254-269
Número de páginas16
PublicaciónJournal of Neurobiology
Volumen40
N.º2
DOI
EstadoPublished - 1999

Financiación

FinanciadoresNúmero del financiador
Eunice Kennedy Shriver National Institute of Child Health and Human DevelopmentT32HD007467

    ASJC Scopus subject areas

    • General Neuroscience
    • Cellular and Molecular Neuroscience

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