β-Amyloid context intensifies vascular smooth muscle cells induced inflammatory response and de-differentiation

Aging Cell. 2013 Jun;12(3):358-69. doi: 10.1111/acel.12056. Epub 2013 Apr 1.

Abstract

Several studies have shown that the accumulation of β-amyloid peptides in the brain parenchyma or vessel wall generates an inflammatory environment. Some even suggest that there is a cause-and-effect relationship between inflammation and the development of Alzheimer's disease and/or cerebral amyloid angiopathy (CAA). Here, we studied the ability of wild-type Aβ1-40 -peptide (the main amyloid peptide that accumulates in the vessel wall in sporadic forms of CAA) to modulate the phenotypic transition of vascular smooth muscle cells (VSMCs) toward an inflammatory/de-differentiated state. We found that Aβ1-40 -peptide alone neither induces an inflammatory response, nor decreases the expression of contractile markers; however, the inflammatory response of VSMCs exposed to Aβ1-40 -peptide prior to the addition of the pro-inflammatory cytokine IL-1β is greatly intensified compared with IL-1β-treated VSMCs previously un-exposed to Aβ1-40 -peptide. Similar conclusions could be drawn when tracking the decline of contractile markers. Furthermore, we found that the mechanism of this potentiation highly depends on an Aβ1-40 preactivation of the PI3 Kinase and possibly NFκB pathway; indeed, blocking the activation of these pathways during Aβ1-40 -peptide treatment completely suppressed the observed potentiation. Finally, strengthening the possible in vivo relevance of our findings, we evidenced that endothelial cells exposed to Aβ1-40 -peptide generate an inflammatory context and have similar effects than the ones described with IL-1β. These results reinforce the idea that intraparietal amyloid deposits triggering adhesion molecules in endothelial cells, contribute to the transition of VSMCs to an inflammatory/de-differentiated phenotype. Therefore, we suggest that acute inflammatory episodes may increase vascular alterations and contribute to the ontogenesis of CAA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alzheimer Disease
  • Amyloid beta-Peptides / metabolism*
  • Animals
  • Brain / blood supply*
  • Cell Dedifferentiation*
  • Cells, Cultured
  • Cerebral Amyloid Angiopathy / immunology
  • Culture Media, Conditioned
  • Enzyme Activation
  • Inflammation / immunology*
  • Interleukin-1beta / pharmacology
  • Mice
  • Muscle, Smooth, Vascular / cytology*
  • Muscle, Smooth, Vascular / immunology*
  • Muscle, Smooth, Vascular / metabolism
  • NF-kappa B / metabolism
  • Peptide Fragments / metabolism*
  • Phosphatidylinositol 3-Kinases / metabolism

Substances

  • Amyloid beta-Peptides
  • Culture Media, Conditioned
  • Interleukin-1beta
  • NF-kappa B
  • Peptide Fragments
  • amyloid beta-protein (1-40)
  • Phosphatidylinositol 3-Kinases