Local zones of endoplasmic reticulum complexity confine cargo in neuronal dendrites

Cell. 2012 Jan 20;148(1-2):309-21. doi: 10.1016/j.cell.2011.11.056.


Following synthesis, integral membrane proteins dwell in the endoplasmic reticulum (ER) for variable periods that are typically rate limiting for plasma membrane delivery. In neurons, the ER extends for hundreds of microns as an anastomosing network throughout highly branched dendrites. However, little is known about the mobility, spatial scales, or dynamic regulation of cargo in the dendritic ER. Here, we show that membrane proteins, including AMPA-type glutamate receptors, rapidly diffuse within the continuous network of dendritic ER but are confined by increased ER complexity at dendritic branch points and near dendritic spines. The spatial range of receptor mobility is rapidly restricted by type I mGluR signaling through a mechanism involving protein kinase C (PKC) and the ER protein CLIMP63. Moreover, local zones of ER complexity compartmentalize ER export and correspond to sites of new dendritic branches. Thus, local control of ER complexity spatially scales secretory trafficking within elaborate dendritic arbors.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Dendrites / metabolism*
  • Embryo, Mammalian / metabolism
  • Endoplasmic Reticulum / metabolism*
  • Hippocampus / cytology
  • Hippocampus / metabolism
  • Male
  • Membrane Proteins / metabolism*
  • Molecular Sequence Data
  • Protein Kinase C / metabolism
  • Rats
  • Receptors, AMPA / metabolism
  • Receptors, Cell Surface / chemistry
  • Receptors, Cell Surface / metabolism
  • Receptors, Metabotropic Glutamate / metabolism
  • Synapses / metabolism


  • CKAP4 protein, rat
  • Membrane Proteins
  • Receptors, AMPA
  • Receptors, Cell Surface
  • Receptors, Metabotropic Glutamate
  • Protein Kinase C