Synchronous onset of NGF and TrkA survival dependence in developing dorsal root ganglia

Fletcher White, Inmaculada Silos-Santiago, Derek C. Molliver, Merry Nishimura, Heidi Phillips, Mariano Barbacid, William D. Snider

Research output: Contribution to journalArticle

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Abstract

Determinations of dorsal root ganglion (DRG) neuron loss in nerve growth factor (NGF) and neurotrophin-3 (NT-3) null mutant mice have supported the concept that neurons can switch neurotrophin dependence by revealing that many neurons must require both of these factors acting either sequentially or simultaneously during development. The situation is complex, however, in that NT-3(-/-) mutant mice show far greater neuron loss than mice deficient in the NT-3 receptor TrkC, suggesting that NT-3 may support many DRG neurons via actions on the NGF receptor TrkA. To assess the possibility of ligand- receptor cross-talk as a developmental mechanism, we have compared the onset of survival dependence of lumbar DRG neurons on NT-3, TrkC, NGF, and TrkA signaling in mice deficient in these molecules as a result of gene targeting. At embryonic day 11.5 (E11.5), virtually all lumbar DRG cells express TrkC mRNA and many require NT-3 and TrkC signaling for survival. In contrast, although many lumbar DRG cells also express TrkA at E11.5, there is little survival dependence on TrkA signaling. By E13.5, most lumbar DRG cells have downregulated TrkC mRNA. The onset of survival dependence on NGF and TrkA- signaling is concurrent and of equal magnitude at E13.5, demonstrating that NT-3 alone does not support DRG neurons via TrkA, nor can NT-3 compensate for the loss of NGF. We conclude that many murine DRG cells require NT-3 for survival before exhibiting NGF dependence and that NT-3 activation of TrkA is unimportant to these early NT-3 survival-promoting actions. We suggest that the discrepancy in cell loss between NT-3(-/-) and trkC(-/-) mutants is attributable to the ability of NT-3 to support DRG neurons via TrkA in the artificial situation where TrkC is absent.

Original languageEnglish (US)
Pages (from-to)4662-4672
Number of pages11
JournalJournal of Neuroscience
Volume16
Issue number15
StatePublished - Aug 1 1996
Externally publishedYes

Fingerprint

Neurotrophin 3
Spinal Ganglia
Nerve Growth Factor
Neurons
trkC Receptor
Receptor Cross-Talk
Nerve Growth Factor Receptor
Messenger RNA
Gene Targeting
Nerve Growth Factors

Keywords

  • DRG development
  • naturally occurring cell death
  • NGF
  • NT-3
  • TrkA
  • TrkC

ASJC Scopus subject areas

  • Neuroscience(all)

Cite this

White, F., Silos-Santiago, I., Molliver, D. C., Nishimura, M., Phillips, H., Barbacid, M., & Snider, W. D. (1996). Synchronous onset of NGF and TrkA survival dependence in developing dorsal root ganglia. Journal of Neuroscience, 16(15), 4662-4672.

Synchronous onset of NGF and TrkA survival dependence in developing dorsal root ganglia. / White, Fletcher; Silos-Santiago, Inmaculada; Molliver, Derek C.; Nishimura, Merry; Phillips, Heidi; Barbacid, Mariano; Snider, William D.

In: Journal of Neuroscience, Vol. 16, No. 15, 01.08.1996, p. 4662-4672.

Research output: Contribution to journalArticle

White, F, Silos-Santiago, I, Molliver, DC, Nishimura, M, Phillips, H, Barbacid, M & Snider, WD 1996, 'Synchronous onset of NGF and TrkA survival dependence in developing dorsal root ganglia', Journal of Neuroscience, vol. 16, no. 15, pp. 4662-4672.
White F, Silos-Santiago I, Molliver DC, Nishimura M, Phillips H, Barbacid M et al. Synchronous onset of NGF and TrkA survival dependence in developing dorsal root ganglia. Journal of Neuroscience. 1996 Aug 1;16(15):4662-4672.
White, Fletcher ; Silos-Santiago, Inmaculada ; Molliver, Derek C. ; Nishimura, Merry ; Phillips, Heidi ; Barbacid, Mariano ; Snider, William D. / Synchronous onset of NGF and TrkA survival dependence in developing dorsal root ganglia. In: Journal of Neuroscience. 1996 ; Vol. 16, No. 15. pp. 4662-4672.
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