Processing of wild-type and mutant familial Alzheimer's disease- associated presenilin-1 in cultured neurons

Conrad C. Weihl, Ghanaysham D. Ghadge, Richard J. Miller, Raymond P. Roos*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

12 Scopus citations


Mutations of presenilin (PS)-1, an endoplasmic reticulum/Golgi transmembrane protein, have been associated with early-onset familial Alzheimer's disease (FAD). In mammalian brain, PS1 exists primarily as its processed fragments; however, the role of this cleavage event in PS1 function remains unclear. Although some investigators have shown that mutant PS1 processing is unaltered (with the exception of PS1-ΔE9, which lacks the cleavage site) in stably transfected cells and PS1-FAD transgenic mice, other investigators have reported altered FAD mutant PS1 and PS2 protein processing in transiently transfected cells and human FAD patients. The present study uses recombinant replication-defective adenoviral vectors to transiently express wild-type (WT) or mutant PS1 in various cells, including primary cultured hippocampal neurons. We show that in contrast to PS1-WT, overexpression of mutant PS1 results in an increased ratio of mutant holoprotein to endoproteolytic products that is dependent on cell type and differentiation state. In addition, mutant PS1 overexpression leads to an increase in caspase-type protease derived fragments above that seen with PS1- WT overexpression. Furthermore, overexpression of at least one mutant significantly alters the processing of coexpressed PS1-WT, suggesting that mutant PS1 may affect PS1-WT function. These findings suggest that a defect in PS1 holoprotein stability may be a general defect seen in cells expressing mutant PS1, especially neuronal cells, and may play a critical role in the pathogenesis of FAD.

Original languageEnglish (US)
Pages (from-to)31-40
Number of pages10
JournalJournal of neurochemistry
Issue number1
StatePublished - 1999


  • Alzheimer's disease
  • Presenilin
  • Proteolytic processing
  • Recombinant adenoviral vector

ASJC Scopus subject areas

  • Biochemistry
  • Cellular and Molecular Neuroscience


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