Altered expression of Notch1 in Alzheimer's disease

PLoS One. 2019 Nov 26;14(11):e0224941. doi: 10.1371/journal.pone.0224941. eCollection 2019.

Abstract

Notch signaling is an evolutionarily conserved pathway that regulates cell-cell interactions through binding of Notch family receptors to their cognate ligands. Notch signaling has an essential role in vascular development and angiogenesis. Recent studies have reported that Notch may be implicated in Alzheimer's disease (AD) pathophysiology. We measured the levels of soluble Notch1 (sNotch1) in the plasma samples from 72 dementia patients (average age 75.1 y), 89 subjects with amnestic mild cognitive impairment (MCI) (average age 73.72 y), and 150 cognitively normal controls (average age 72.34 y). Plasma levels of sNotch1 were 25.27% lower in dementia patients as compared to healthy control subjects. However, the level of Notch1 protein was significantly increased in human brain microvascular endothelial cells (HBMECs) after amyloid-beta treatment. Also, Notch1 mRNA level was significantly increased in HBMECs and iPSC-derived neuronal cells from AD patient compared to normal control. These results indicate that altered expression of Notch1 might be associated with the risk of Alzheimer's disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ADAM10 Protein / genetics
  • ADAM10 Protein / metabolism
  • Aged
  • Aged, 80 and over
  • Alzheimer Disease / blood
  • Alzheimer Disease / metabolism*
  • Amyloid beta-Peptides / metabolism
  • Case-Control Studies
  • Dementia / metabolism
  • Female
  • Human Umbilical Vein Endothelial Cells / metabolism
  • Humans
  • Induced Pluripotent Stem Cells / metabolism
  • Male
  • Middle Aged
  • Neurons / metabolism
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Receptor, Notch1 / blood
  • Receptor, Notch1 / genetics
  • Receptor, Notch1 / metabolism*

Substances

  • Amyloid beta-Peptides
  • NOTCH1 protein, human
  • RNA, Messenger
  • Receptor, Notch1
  • ADAM10 Protein

Grants and funding

This work was supported by the Korea Centers for Disease Control and Prevention (KCDC) 2016-NG62002-00, 2017-NI62001-00, (http://www.cdc.go.kr). The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.