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  4. Local and long-range endogenous resting potential gradients antagonistically regulate apoptosis and proliferation in the embryonic CNS

Local and long-range endogenous resting potential gradients antagonistically regulate apoptosis and proliferation in the embryonic CNS

Int J Dev Biol, 2015 · DOI: 10.1387/ijdb.150197ml · Published: January 1, 2015

PhysiologyNeurologyGenetics

Simple Explanation

This study explores how bioelectric signals, specifically transmembrane voltage potentials (Vmem), influence brain development in Xenopus embryos. These signals act as instructive factors, guiding processes like eye and brain formation. The research found that disrupting local bioelectric signals within the developing neural tube increases cell death (apoptosis) and decreases cell division (proliferation), leading to brain mispatterning. Conversely, disrupting bioelectric signals from distant regions has the opposite effect, decreasing apoptosis and increasing proliferation, while maintaining normal brain patterning. The combined disruption of both local and distant bioelectric signals results in opposing effects on cell death and division. These findings suggest that brain and spinal cord development relies on a binary control system of local and long-range bioelectric signals to regulate apoptosis and proliferation.

Study Duration
Not specified
Participants
Xenopus laevis embryos
Evidence Level
Not specified

Key Findings

  • 1
    Disrupting local bioelectric signals in the developing neural tube increases apoptosis and decreases proliferation, leading to brain mispatterning.
  • 2
    Disrupting distant bioelectric signals decreases apoptosis and increases proliferation in the brain, without disrupting normal brain patterning.
  • 3
    Local and distant bioelectric signals have antagonistic effects on apoptosis and proliferation, forming a binary control system for fine-tuning these processes in the developing CNS.

Research Summary

This study investigates the role of transmembrane voltage potentials (Vmem) in regulating apoptosis and proliferation during embryonic CNS development using Xenopus laevis embryos. Disrupting local Vmem signals increases apoptosis and decreases proliferation, causing brain mispatterning. Disrupting distant Vmem signals decreases apoptosis and increases proliferation in the brain. Combining both local and distant disruptions leads to antagonistic effects, suggesting a binary control system. The findings highlight the importance of bioelectric signals in fine-tuning apoptosis-proliferation balance for proper brain and spinal cord development, offering potential strategies for interventions in birth defects and degenerative diseases.

Practical Implications

Diagnostic Modality

Bioelectric state can be used as a diagnostic marker for CNS-related birth defects and degenerative diseases.

Therapeutic Intervention

Modulating bioelectric signals, particularly through ion channel drugs, can be a convenient intervention parameter for treating CNS disorders.

Regenerative Medicine

Targeting non-neural tissues with electroceuticals can be a strategy for manipulating neurogenesis and neural patterning in regenerative medicine.

Study Limitations

  • 1
    The specific molecular mechanisms by which bioelectric signals regulate apoptosis and proliferation are not fully understood.
  • 2
    The study focuses on Xenopus embryos, and the findings may not be directly applicable to other species or humans.
  • 3
    The interplay between local and long-distance bioelectric transduction mechanisms requires further investigation.

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