Starvation triggers Abeta42 generation from human umbilical vascular endothelial cells

FEBS Lett. 2010 Jul 16;584(14):3101-6. doi: 10.1016/j.febslet.2010.05.048. Epub 2010 Jun 1.

Abstract

Cerebral amyloid angiopathy is a common feature in Alzheimer's disease (AD), which is characterized by amyloid deposit around brain vessels including capillaries. The origin of the amyloid protein of CAA remains controversial. In our work, we provide data to show that primary umbilical vein endothelial cells (HUVEC) harbor APP processing secretases and can produce Abeta(42) under starvation. Starvation can increase the secretion of Abeta(42) by altering the expression of beta-secretases (BACE1) and gamma-secretases (APH and PEN2). This process is regulated by macroautophagy. Suppression of macroautophagy induction by 3MA further increased the level of Abeta(42) produced under starvation in HUVECs. These results suggest that starvation-induced Abeta(42) secretion might contribute to the formation of CAA and hence vascular degeneration in AD.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alzheimer Disease / metabolism
  • Amyloid Precursor Protein Secretases / metabolism*
  • Amyloid beta-Protein Precursor
  • Animals
  • Blood Vessels / metabolism
  • Brain / metabolism
  • Cerebral Amyloid Angiopathy / metabolism
  • Endothelial Cells / metabolism
  • Humans
  • Mice
  • Mice, Transgenic
  • Protease Nexins
  • Receptors, Cell Surface
  • Starvation / metabolism
  • Umbilical Veins / metabolism
  • Umbilicus

Substances

  • APP protein, human
  • Amyloid beta-Protein Precursor
  • Protease Nexins
  • Receptors, Cell Surface
  • Amyloid Precursor Protein Secretases