Distinct subsets of Syt-IV/BDNF vesicles are sorted to axons versus dendrites and recruited to synapses by activity

J Neurosci. 2012 Apr 18;32(16):5398-413. doi: 10.1523/JNEUROSCI.4515-11.2012.

Abstract

BDNF plays a critical role in the regulation of synaptic strength and is essential for long-term potentiation, a phenomenon that underlies learning and memory. However, whether BDNF acts in a diffuse manner or is targeted to specific neuronal subcompartments or synaptic sites to affect circuit function remains unknown. Here, using photoactivation of BDNF or syt-IV (a regulator of exocytosis present on BDNF-containing vesicles) in transfected rat hippocampal neurons, we discovered that distinct subsets of BDNF vesicles are targeted to axons versus dendrites and are not shared between these compartments. Moreover, syt-IV- and BDNF-harboring vesicles are recruited to both presynaptic and postsynaptic sites in response to increased neuronal activity. Finally, using syt-IV knockout mouse neurons, we found that syt-IV is necessary for both presynaptic and postsynaptic scaling of synaptic strength in response to changes in network activity. These findings demonstrate that BDNF-containing vesicles can be targeted to specific sites in neurons and suggest that syt-IV-regulated BDNF secretion is subject to spatial control to regulate synaptic function in a site-specific manner.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Activated-Leukocyte Cell Adhesion Molecule / metabolism
  • Animals
  • Animals, Newborn
  • Axons / metabolism*
  • Brain-Derived Neurotrophic Factor / genetics
  • Brain-Derived Neurotrophic Factor / metabolism
  • Cells, Cultured
  • Coculture Techniques
  • Colforsin / pharmacology
  • Dendrites / metabolism*
  • Disks Large Homolog 4 Protein
  • Embryo, Mammalian
  • Excitatory Amino Acid Agents / pharmacology
  • Excitatory Postsynaptic Potentials / drug effects
  • Excitatory Postsynaptic Potentials / genetics
  • Female
  • Glycine / pharmacology
  • Hippocampus / cytology
  • Humans
  • Intracellular Signaling Peptides and Proteins / metabolism
  • Luminescent Proteins / genetics
  • Luminescent Proteins / metabolism
  • Male
  • Membrane Proteins / metabolism
  • Mice
  • Mice, Knockout
  • Microtubule-Associated Proteins / metabolism
  • Neurons / cytology*
  • Neurons / metabolism
  • Patch-Clamp Techniques
  • Rats
  • Receptors, AMPA / metabolism
  • Sodium Channel Blockers / pharmacology
  • Synapses / physiology
  • Synaptic Vesicles / classification*
  • Synaptic Vesicles / metabolism*
  • Synaptophysin / metabolism
  • Synaptotagmins / deficiency
  • Synaptotagmins / metabolism*
  • Tetrodotoxin / pharmacology
  • Time Factors
  • Transfection
  • Vesicular Glutamate Transport Protein 1 / metabolism
  • Vesicular Inhibitory Amino Acid Transport Proteins / metabolism

Substances

  • Activated-Leukocyte Cell Adhesion Molecule
  • Brain-Derived Neurotrophic Factor
  • Disks Large Homolog 4 Protein
  • Dlg4 protein, rat
  • Excitatory Amino Acid Agents
  • Intracellular Signaling Peptides and Proteins
  • Luminescent Proteins
  • MAP2 protein, human
  • Membrane Proteins
  • Microtubule-Associated Proteins
  • Receptors, AMPA
  • SLC32A1 protein, human
  • Sodium Channel Blockers
  • Synaptophysin
  • Vesicular Glutamate Transport Protein 1
  • Vesicular Inhibitory Amino Acid Transport Proteins
  • Synaptotagmins
  • Colforsin
  • Tetrodotoxin
  • glutamate receptor ionotropic, AMPA 2
  • Glycine