Volume 8 Supplement 1

Molecular Neurodegeneration: Basic biology and disease pathways

Open Access

Regulation of dynamic BACE1 trafficking in neurons

  • Virginie Buggia-Prévot1,
  • Celia G Fernandez3,
  • Sean Riordan4,
  • Kulandaivelu S Vetrivel1,
  • Vinod Udayar6,
  • Aureliane Elie1,
  • Margaret Lefkow3,
  • Jelita Roseman1,
  • Xavier Meckler1,
  • Sohinee Bhattacharyya6,
  • Manju George7,
  • Jack Waters5,
  • Vytautas P Bindokas2,
  • Angèle T Parent1,
  • Lawrence Rajendran6,
  • Hamid Band7,
  • Robert Vassar4 and
  • Gopal Thinakaran1, 3
Molecular Neurodegeneration20138(Suppl 1):O8


Published: 13 September 2013

Proteolytic processing of amyloid precursor protein (APP) by β-site APP cleaving enzyme 1 (BACE1) and γ-secretase generates Aβ peptides. APP is constitutively trafficked through the secretory and endocytic pathways in cultured cells and neurons. The identities of cellular organelles and sorting pathways involved in amyloidogenic processing of APP have been extensively investigated. Although a consensus has not yet emerged, there is a general agreement from biochemical and genetic studies on the importance of endocytic APP trafficking for Aβ production. In neurons, APP is trafficked anterogradely along peripheral and central axons, and proteolytically processed during transit. Recent in vivo studies estimated that ~70% of Aβ released in the brain requires ongoing endocytosis, and synaptic activity regulates the vast majority of this endocytosis-dependent Aβ. BACE1 cleavage is thought to be the rate-limiting step in amyloidogenic processing of APP. Little, however, is known about endocytic BACE1 sorting and dynamic transport in neurons. We investigated BACE1 trafficking in cultured hippocampal neurons using live-cell imaging and selective labeling. This approach revealed dynamic neuronal transport of internalized BACE1 in dendrites and axons. BACE1 was transported in vesicles that were positive for markers of recycling endosomes. Dominant-negative expression and siRNA knock-down of proteins involved in endocytic transit revealed that BACE1 is dynamically transported in recycling endosomes and this process significantly contributes to amyloidogenic APP processing. Our results suggest that BACE1 trafficking in neuronal recycling endosomes is likely relevant for presynaptic Aβ production and contributes to Alzheimer’s disease pathogenesis.

Authors’ Affiliations

Departments of Neurobiology, Neurology, and Pathology, The University of Chicago
Department of Pharmacological and Physiological Sciences, The University of Chicago
Committee on Neurobiology, The University of Chicago
Department of Cell and Molecular Biology, Feinberg School of Medicine, Northwestern University
Department of Physiology, Feinberg School of Medicine, Northwestern University
Systems and Cell Biology of Neurodegeneration, Division of Psychiatry Research, University of Zurich
Eppley Institute for Research in Cancer and Allied Diseases and Eppley Cancer Center, University of Nebraska Medical Center


© Buggia-Prévot et al; licensee BioMed Central Ltd. 2013

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.