The molecular physiology of activity-dependent bulk endocytosis of synaptic vesicles

J Neurochem. 2009 Nov;111(4):901-14. doi: 10.1111/j.1471-4159.2009.06384.x. Epub 2009 Sep 16.


Central nerve terminals release neurotransmitter in response to a wide variety of stimuli. Because maintenance of neurotransmitter release is dependent on the continual supply of synaptic vesicles (SVs), nerve terminals possess an array of endocytosis modes to retrieve and recycle SV membrane and proteins. During mild stimulation conditions, single SV retrieval modes such as clathrin-mediated endocytosis predominate. However, during increased neuronal activity, additional SV retrieval capacity is required, which is provided by activity-dependent bulk endocytosis (ADBE). ADBE is the dominant SV retrieval mechanism during elevated neuronal activity. It is a high capacity SV retrieval mode that is immediately triggered during such stimulation conditions. This review will summarize the current knowledge regarding the molecular mechanism of ADBE, including molecules required for its triggering and subsequent steps, including SV budding from bulk endosomes. The molecular relationship between ADBE and the SV reserve pool will also be discussed. It is becoming clear that an understanding of the molecular physiology of ADBE will be of critical importance in attempts to modulate both normal and abnormal synaptic function during intense neuronal activity.

Publication types

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

MeSH terms

  • Actins / metabolism
  • Animals
  • Calcineurin / metabolism
  • Dynamin I / metabolism
  • Endocytosis / genetics
  • Endocytosis / physiology*
  • Lipid Metabolism / physiology
  • Nerve Tissue Proteins / metabolism
  • Neurons / cytology*
  • Presynaptic Terminals / physiology*
  • Presynaptic Terminals / ultrastructure
  • Synaptic Vesicles / physiology*


  • Actins
  • Nerve Tissue Proteins
  • Calcineurin
  • Dynamin I