APC2 controls dendrite development by promoting microtubule dynamics

Olga I Kahn, Philipp Schätzle, Dieudonnée van de Willige, Roderick P Tas, Feline W Lindhout, Sybren Portegies, Lukas C Kapitein, Casper C Hoogenraad

Research output: Contribution to journalArticleAcademicpeer-review


Mixed polarity microtubule organization is the signature characteristic of vertebrate dendrites. Oppositely oriented microtubules form the basis for selective cargo trafficking in neurons, however the mechanisms that establish and maintain this organization are unclear. Here, we show that APC2, the brain-specific homolog of tumor-suppressor protein adenomatous polyposis coli (APC), promotes dynamics of minus-end-out microtubules in dendrites. We found that APC2 localizes as distinct clusters along microtubule bundles in dendrites and that this localization is driven by LC8-binding and two separate microtubule-interacting domains. Depletion of APC2 reduces the plus end dynamics of minus-end-out oriented microtubules, increases microtubule sliding, and causes defects in dendritic morphology. We propose a model in which APC2 regulates dendrite development by promoting dynamics of minus-end-out microtubules.

Original languageEnglish
Article number2773
Number of pages17
JournalNature Communications
Publication statusPublished - 17 Jul 2018


  • Animals
  • COS Cells
  • Cercopithecus aethiops
  • Cytoplasmic Dyneins/genetics
  • Cytoskeletal Proteins/genetics
  • Dendrites/metabolism
  • Embryo, Mammalian
  • Gene Expression Regulation
  • Genes, Reporter
  • Green Fluorescent Proteins/genetics
  • HEK293 Cells
  • Hippocampus/cytology
  • Humans
  • Luminescent Proteins/genetics
  • Microtubules/metabolism
  • Molecular Imaging
  • Neurogenesis/genetics
  • Neurons/metabolism
  • Primary Cell Culture
  • Protein Binding
  • Protein Isoforms/genetics
  • Rats
  • Rats, Wistar
  • Signal Transduction
  • Time-Lapse Imaging


Dive into the research topics of 'APC2 controls dendrite development by promoting microtubule dynamics'. Together they form a unique fingerprint.

Cite this