SEPT8 modulates β-amyloidogenic processing of APP by affecting the sorting and accumulation of BACE1

J Cell Sci. 2016 Jun 1;129(11):2224-38. doi: 10.1242/jcs.185215. Epub 2016 Apr 15.

Abstract

Dysfunction and loss of synapses are early pathogenic events in Alzheimer's disease. A central step in the generation of toxic amyloid-β (Aβ) peptides is the cleavage of amyloid precursor protein (APP) by β-site APP-cleaving enzyme (BACE1). Here, we have elucidated whether downregulation of septin (SEPT) protein family members, which are implicated in synaptic plasticity and vesicular trafficking, affects APP processing and Aβ generation. SEPT8 was found to reduce soluble APPβ and Aβ levels in neuronal cells through a post-translational mechanism leading to decreased levels of BACE1 protein. In the human temporal cortex, we identified alterations in the expression of specific SEPT8 transcript variants in a manner that correlated with Alzheimer's-disease-related neurofibrillary pathology. These changes were associated with altered β-secretase activity. We also discovered that the overexpression of a specific Alzheimer's-disease-associated SEPT8 transcript variant increased the levels of BACE1 and Aβ peptides in neuronal cells. These changes were related to an increased half-life of BACE1 and the localization of BACE1 in recycling endosomes. These data suggest that SEPT8 modulates β-amyloidogenic processing of APP through a mechanism affecting the intracellular sorting and accumulation of BACE1.

Keywords: Alzheimer's disease; Amyloid precursor protein; Amyloid-β; BACE1; SEPT8.

MeSH terms

  • Alzheimer Disease / genetics
  • Alzheimer Disease / pathology
  • Amyloid Precursor Protein Secretases / metabolism*
  • Amyloid beta-Peptides / metabolism*
  • Animals
  • Aspartic Acid Endopeptidases / metabolism*
  • Cell Line, Tumor
  • Down-Regulation
  • Gene Expression Profiling
  • HEK293 Cells
  • Half-Life
  • Hippocampus / pathology
  • Humans
  • Intracellular Space / metabolism
  • Mice, Inbred C57BL
  • Models, Biological
  • Neurofibrillary Tangles / genetics
  • Neurofibrillary Tangles / pathology
  • Neurons / metabolism
  • Protein Processing, Post-Translational*
  • Protein Stability
  • Protein Transport
  • RNA Interference
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Septins / genetics
  • Septins / metabolism*
  • Temporal Lobe / metabolism
  • Temporal Lobe / pathology

Substances

  • Amyloid beta-Peptides
  • RNA, Messenger
  • SEPT8 protein, mouse
  • Amyloid Precursor Protein Secretases
  • Aspartic Acid Endopeptidases
  • BACE1 protein, human
  • Bace1 protein, mouse
  • SEPTIN8 protein, human
  • Septins