Reduction of intramuscular nerve branching and synaptogenesis is correlated with decreased motoneuron survival

J Tang1, L Landmesser

  • 1Department of Physiology and Neurobiology, University of Connecticut, Storrs 06269-3042.

Insights

Removing polysialic acid (PSA) reduces nerve branching and synapse formation in developing chicken embryos. This reduction in neural connections correlates with decreased motor neuron survival, independent of muscle activity.

Area of Science:

  • Developmental Neuroscience
  • Neurobiology
  • Cell Biology

Background:

  • Neuromuscular activity blockade enhances motor neuron survival, nerve branching, and synaptogenesis.
  • Enhanced motor neuron survival may stem from increased trophic factor uptake via more branches/synapses, not increased factor production.

Purpose of the Study:

  • To investigate if removing polysialic acid (PSA) reduces synapse formation.
  • To determine if reduced synapse formation correlates with decreased motor neuron survival.
  • To assess the role of PSA in motor neuron survival during development, independent of muscle activity.

Main Methods:

  • Removal of PSA using PSA-specific endoneuraminidase (endo N) in embryonic chicken limbs from day 6 (E6) to E9.
  • Quantification of synapse numbers in the posterior iliotibialis muscle at E6.5 and E7.5-E8.
  • Assessment of total motoneuron counts at E7.5-E8 and E10.

Main Results:

  • PSA removal significantly reduced synapse numbers at the onset and middle of the motor neuron cell death period.
  • Total motoneuron counts were significantly decreased in PSA-depleted embryos compared to controls.
  • Embryonic motility and muscle activation patterns remained unaltered by PSA removal.

Conclusions:

  • Reduced intramuscular nerve branching and synapse formation due to PSA removal negatively impact motor neuron survival.
  • The findings suggest PSA plays a crucial role in supporting motor neuron survival through its influence on neural connectivity.
  • This study isolates the effects of PSA on neural development from confounding factors like neuromuscular activity blockade.

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