Inhibition of clathrin-mediated endocytosis prevents amyloid β-induced axonal damage

Neurobiol Aging. 2015 May;36(5):1808-19. doi: 10.1016/j.neurobiolaging.2015.02.005. Epub 2015 Feb 13.

Abstract

Amyloid β (Aβ)-induced axonal degeneration is a major cause of Alzheimer's disease (AD) pathology. However, the critical target to prevent Aβ-induced axonal degeneration remains unknown. Here, we analyzed growth cone collapse elicited by Aβ, a putative early Aβ-induced event in axons. Although no study has yet shown influence of Aβ on the growth cone, we first visualized Aβ-initiated growth cone collapse in cultured neurons. Furthermore, we determined that the collapse was triggered by clathrin-mediated endocytosis probably via Aβ-Ca(2+) signaling. The inhibition of clathrin-mediated endocytosis prevented Aβ-induced axonal loss both in vitro and in vivo and prevented memory impairment in an AD mouse model. Our results clarified the important role of clathrin-mediated endocytosis in Aβ-induced collapse of growth cone that leads to axonal degeneration and memory impairment.

Keywords: Amyloid β (Aβ); Axonal degeneration; Clathrin-mediated endocytosis; Growth cone collapse; Memory impairment.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alzheimer Disease / etiology*
  • Alzheimer Disease / pathology*
  • Amyloid beta-Peptides / adverse effects*
  • Amyloid beta-Peptides / metabolism*
  • Animals
  • Axons / metabolism*
  • Axons / pathology*
  • Calcium Signaling / physiology
  • Cells, Cultured
  • Cerebral Cortex / cytology
  • Clathrin / physiology
  • Disease Models, Animal
  • Endocytosis / physiology*
  • Growth Cones / metabolism
  • Growth Cones / pathology
  • Memory Disorders / etiology
  • Mice, Inbred Strains
  • Nerve Degeneration / etiology*
  • Neurons

Substances

  • Amyloid beta-Peptides
  • Clathrin