Elevated Cerebrospinal Fluid and Plasma N-Cadherin in Alzheimer Disease

J Neuropathol Exp Neurol. 2020 May 1;79(5):484-492. doi: 10.1093/jnen/nlaa019.

Abstract

N-cadherin is a synaptic adhesion molecule stabilizing synaptic cell structure and function. Cleavage of N-cadherin by γ-secretase produces a C-terminal fragment, which is increased in the brains of Alzheimer disease (AD) patients. Here, we investigated the relationship between fluid N-cadherin levels and AD pathology. We first showed that the cleaved levels of N-cadherin were increased in homogenates of postmortem brain from AD patients compared with that in non-AD patients. We found that cleaved N-cadherin levels in the cerebrospinal fluid were increased in AD dementia compared with that in healthy control. ELISA results revealed that plasma levels of N-cadherin in 76 patients with AD were higher than those in 133 healthy control subjects. The N-cadherin levels in the brains of an AD mouse model, APP Swedish/PS1delE9 Tg (APP Tg) were reduced compared with that in control. The N-terminal fragment of N-cadherin produced by cleavage at a plasma membrane was detected extravascularly, accumulated in senile plaques in the cortex of an APP Tg mouse. In addition, N-cadherin plasma levels were increased in APP Tg mice. Collectively, our study suggests that alteration of N-cadherin levels might be associated with AD pathology.

Keywords: Alzheimer disease; Brain; Cerebrospinal fluid; Dementia; N-cadherin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • Alzheimer Disease / cerebrospinal fluid*
  • Amyloid beta-Peptides / administration & dosage
  • Animals
  • Antigens, CD / blood*
  • Antigens, CD / cerebrospinal fluid*
  • Brain / blood supply
  • Brain Chemistry*
  • Cadherins / blood*
  • Cadherins / cerebrospinal fluid*
  • Cells, Cultured
  • Disease Models, Animal
  • Female
  • Humans
  • Male
  • Mice, Transgenic
  • Microglia / drug effects
  • Microglia / metabolism

Substances

  • Amyloid beta-Peptides
  • Antigens, CD
  • CDH2 protein, human
  • Cadherins