Activity-dependent trafficking of lysosomes in dendrites and dendritic spines

J Cell Biol. 2017 Aug 7;216(8):2499-2513. doi: 10.1083/jcb.201704068. Epub 2017 Jun 19.

Abstract

In neurons, lysosomes, which degrade membrane and cytoplasmic components, are thought to primarily reside in somatic and axonal compartments, but there is little understanding of their distribution and function in dendrites. Here, we used conventional and two-photon imaging and electron microscopy to show that lysosomes traffic bidirectionally in dendrites and are present in dendritic spines. We find that lysosome inhibition alters their mobility and also decreases dendritic spine number. Furthermore, perturbing microtubule and actin cytoskeletal dynamics has an inverse relationship on the distribution and motility of lysosomes in dendrites. We also find trafficking of lysosomes is correlated with synaptic α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid-type glutamate receptors. Strikingly, lysosomes traffic to dendritic spines in an activity-dependent manner and can be recruited to individual spines in response to local activation. These data indicate the position of lysosomes is regulated by synaptic activity and thus plays an instructive role in the turnover of synaptic membrane proteins.

Publication types

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

MeSH terms

  • Actin Cytoskeleton / metabolism
  • Animals
  • Animals, Newborn
  • Dendrites / metabolism*
  • Dendrites / ultrastructure
  • Dendritic Spines / metabolism*
  • Dendritic Spines / ultrastructure
  • Female
  • HEK293 Cells
  • Hippocampus / metabolism*
  • Hippocampus / ultrastructure
  • Humans
  • Lysosomes / metabolism*
  • Lysosomes / ultrastructure
  • Male
  • Membrane Proteins / metabolism*
  • Microscopy, Electron
  • Microscopy, Fluorescence, Multiphoton
  • Microscopy, Video
  • Microtubules / metabolism
  • Nerve Tissue Proteins / metabolism*
  • Protein Denaturation
  • Rats, Sprague-Dawley
  • Receptors, Glutamate / metabolism
  • Receptors, N-Methyl-D-Aspartate / metabolism
  • Synaptic Membranes / metabolism*
  • Time Factors
  • Time-Lapse Imaging
  • Transfection

Substances

  • Membrane Proteins
  • Nerve Tissue Proteins
  • Receptors, Glutamate
  • Receptors, N-Methyl-D-Aspartate
  • alpha-amino-3-hydroxy-5-methylisoxazole-4-propionic acid subtype glutamate receptor, human