Alteration of the microRNA network during the progression of Alzheimer's disease

  • Pierre Lau
  • , Koen Bossers
  • , Rekin's Janky
  • , Evgenia Salta
  • , Carlo Sala Frigerio
  • , Shahar Barbash
  • , Roy Rothman
  • , Annerieke S.R. Sierksma
  • , Amantha Thathiah
  • , David Greenberg
  • , Aikaterini S. Papadopoulou
  • , Tilmann Achsel
  • , Torik Ayoubi
  • , Hermona Soreq
  • , Joost Verhaagen
  • , Dick F. Swaab
  • , Stein Aerts
  • , Bart De Strooper*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

418 Scopus citations

Abstract

An overview of miRNAs altered in Alzheimer's disease (AD) was established by profiling the hippocampus of a cohort of 41 late-onset AD (LOAD) patients and 23 controls, showing deregulation of 35 miRNAs. Profiling of miRNAs in the prefrontal cortex of a second independent cohort of 49 patients grouped by Braak stages revealed 41 deregulated miRNAs. We focused on miR-132-3p which is strongly altered in both brain areas. Downregulation of this miRNA occurs already at Braak stages III and IV, before loss of neuron-specific miRNAs. Next-generation sequencing confirmed a strong decrease of miR-132-3p and of three family-related miRNAs encoded by the same miRNA cluster on chromosome 17. Deregulation of miR-132-3p in AD brain appears to occur mainly in neurons displaying Tau hyper-phosphorylation. We provide evidence that miR-132-3p may contribute to disease progression through aberrant regulation of mRNA targets in the Tau network. The transcription factor (TF) FOXO1a appears to be a key target of miR-132-3p in this pathway.

Original languageEnglish
Pages (from-to)1613-1634
Number of pages22
JournalEMBO Molecular Medicine
Volume5
Issue number10
DOIs
StatePublished - Oct 2013

Keywords

  • Alzheimer's disease
  • Hippocampus
  • MiR-132-3p
  • MicroRNA
  • Prefrontal cortex

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