Protein markers for Alzheimer in the frontal cortex and cerebellum

G. Verdile, A. Gnjec, J. Miklossy, J. Fonte, G. Veurink, K. Bates, B. Kakulas, P. D. Mehta, E. A. Milward, N. Tan, R. Lareu, D. Lim, A. Dharmarajan, Ralph N. Martins*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

25 Citations (Scopus)


Objective: To compare proteins related to Alzheimer disease (AD) in the frontal cortex and cerebellum of subjects with early-onset AD (EOAD) with or without presenilin 1 (PS1) mutations with sporadic late-onset AD (LOAD) and nondemented control subjects. Methods: Immunohistochemistry, immunoblot analysis, and ELISA were used to detect and assess protein levels in brain. Results: In EOAD and to a lesser extent in LOAD, there was increased amyloid beta (Aβ) deposition (by immunohistochemistry), increased soluble Aβ (by immunoblot analysis), and specific increases in Aβ40 and Aβ42 (by ELISA) in the frontal cortex and, in some cases, in the cerebellum. Surprisingly, immunoblot analysis revealed reduced levels of PS1 in many of the subjects with EOAD with or without PS1 mutations. In those PS1 mutation-bearing subjects with the highest Aβ, PS1 was barely, if at all, detectable. This decrease in PS1 was specific and not attributable solely to neuronal loss because amyloid precursor protein (APP) and the PS1-interacting protein β-catenin levels were unchanged. Conclusions: This study shows that in the frontal cortex and cerebellum from Alzheimer disease patients harboring certain presenilin 1 mutations, high levels of amyloid beta are associated with low levels of presenilin 1. The study provides the premise for further investigation of mechanisms underlying the downregulation of presenilin 1, which may have considerable pathogenic and therapeutic relevance.

Original languageEnglish
Pages (from-to)1385-1392
Number of pages8
Issue number8
Publication statusPublished - 26 Oct 2004
Externally publishedYes


Dive into the research topics of 'Protein markers for Alzheimer in the frontal cortex and cerebellum'. Together they form a unique fingerprint.

Cite this