A novel polish presenilin-1 mutation (P117L) is associated with familial Alzheimer's disease and leads to death as early as the age of 28 years

Thomas Wisniewski, Wieslaw K. Dowjat, Joseph D. Buxbaum, Olga Khorkova, Spiros Efthimiopoulos, Jerzy Kulczycki, Wanda Lojkowska, Jerzy Wegiel, H. M. Wisniewski, B. Frangione

Research output: Contribution to journalArticlepeer-review

100 Scopus citations

Abstract

THE majority of early-onset familial Alzheimer's disease (FAD) is associated with mutations in the presenilin-1 (PS1) gene. We describe a novel Polish PS1 mutation of Pro117Leu, associated with the earliest average age of onset and death so far reported in a PS-linked, FAD kindred. Human kidney 293 and mouse neuroblastoma N2a cells were stably transfected with wild-type and PS1 P117L. There was a significant increase in the amyloid β42/40 ratio in the N2a P117L PS1 transfected cells compared with N2a transfected with wild- type PS1. What role PS has in the pathogenesis of AD remains to be determined, however, the severity of the clinical picture associated with this PS1 mutation stresses the importance of presenilin.

Original languageEnglish
Pages (from-to)217-221
Number of pages5
JournalNeuroReport
Volume9
Issue number2
DOIs
StatePublished - 26 Jan 1998

Keywords

  • Alzheimer's disease
  • Amyloid β
  • Mutation
  • Presenilin
  • Transfection

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