BDNF supports mammalian chemoafferent neurons in vitro and following peripheral target removal in vivo

Dev Biol. 1994 Dec;166(2):801-11. doi: 10.1006/dbio.1994.1358.

Abstract

Chemoreceptor neurons innervating the rat carotid body were used as a model system to define target regulation of visceral sensory development in fetal and newborn animals. In vitro, chemoafferents were selectively supported by coculture with the carotid body or by treatment with trkB ligands [brain-derived neurotrophic factor (BDNF) and neurotrophin-4], whereas nerve growth factor and neurotrophin 3 had no effect. In vivo, chemoafferent neurons died following carotid body removal at birth, indicating a predominant role of peripheral, rather than central, targets in mediating survival at this stage. However, in the absence of target tissues, a large proportion of carotid body afferents could be rescued by implants containing BDNF. Moreover, BDNF mRNA was detected in the newborn carotid body by reverse transcriptase polymerase chain reaction. These data provide the first demonstration that BDNF can substitute for peripheral target support of sensory neuron survival in vivo and indicate that trkB ligands may be particularly important for development of visceral afferents involved in cardiorespiratory control.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Afferent Pathways
  • Animals
  • Base Sequence
  • Brain-Derived Neurotrophic Factor
  • Carotid Body / physiology*
  • Chemoreceptor Cells / physiology*
  • DNA Primers / chemistry
  • Ganglia / physiology
  • Gene Expression Regulation, Developmental
  • Growth Substances / pharmacology*
  • Molecular Sequence Data
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / pharmacology*
  • Neurofilament Proteins / metabolism
  • RNA, Messenger / genetics
  • Rats
  • Rats, Sprague-Dawley
  • Tyrosine 3-Monooxygenase / metabolism

Substances

  • Brain-Derived Neurotrophic Factor
  • DNA Primers
  • Growth Substances
  • Nerve Tissue Proteins
  • Neurofilament Proteins
  • RNA, Messenger
  • Tyrosine 3-Monooxygenase