Proceedings of the National Academy of Sciences · 2012 · 189 citations · 31 references
Life SciencesNeurobiologyNeuroscienceDevelopmental NeuroscienceMolecular NeuroscienceSignal TransductionNeural DevelopmentNeurochemical Signaling PathwaysNeuromuscular JunctionNeurotrophic FactorsSynaptic Strength RegulationSynaptic TransmissionActivity-dependent Synapse EliminationAxon TerminalsDevelopmental Synapse EliminationNeurotrophic Factor SignalingNeurotrophin Receptor SignalingSynapse Elimination In NeurodevelopmentSynaptic CompetitionTrkb Signaling
Formation of specific neuronal connections often involves competition between adjacent axons, leading to stabilization of the active terminal, while retraction of the less active ones. The underlying molecular mechanisms remain unknown. We show that activity-dependent conversion of pro-brain-derived neurotrophic factor (proBDNF) to mature (m)BDNF mediates synaptic competition. Stimulation of motoneurons triggers proteolytic conversion of proBDNF to mBDNF at nerve terminals. In Xenopus nerve-muscle cocultures, in which two motoneurons innervate one myocyte, proBDNF-p75(NTR) signaling promotes retraction of the less active terminal, whereas mBDNF-tyrosine-related kinase B (TrkB) p75NTR (p75 neurotrophin receptor) facilitates stabilization of the active one. Thus, proBDNF and mBDNF may serve as potential "punishment" and "reward" signals for inactive and active terminals, respectively, and activity-dependent conversion of proBDNF to mBDNF may regulate synapse elimination.
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Cleavage of proBDNF by tPA/Plasmin Is Essential for Long-Term Hippocampal Plasticity
Petti T. Pang, Henry Teng, Eugene Zaitsev et al. · Science · 2004 · 1.1K citations