Background: Neurofibrillary tangles and senile plaques are hallmarks of Alzheimer's disease (AD) although the molecular basis of their coexistence remains elusive. The peptidyl-prolyl cis/trans isomerase Pin1 acts on both tau and amyloid precursor protein to regulate their functions by influencing tau phosphorylation and amyloid precursor protein processing. Objective: In order to identify potential biomarkers for AD in easily accessible cells and to gain insight into the relationship between the brain and peripheral compartments in AD pathology, we investigated Pin1 expression and activity in the peripheral blood mononuclear cells of subjects with late-onset AD (LOAD) and age-matched controls (CT). Methods: Gene and protein expression, promoter methylation, Ser 16 phosphorylation and activity of Pin1 were evaluated in 32 samples from subjects with LOAD and in 28 samples from CT. Results: In LOAD subjects, there was a statistically significant reduction in Ser 16 phosphorylation (-30%; p = 0.041) and promoter methylation (-8%; p = 0.001), whereas Pin1 expression was significantly increased (+74%; p = 0.018). Conclusion: The modifications of Pin1 found in LOAD subjects support its involvement in the pathogenesis of the disease with an important role being played by epigenetic mechanisms. Copyright © 2012 S. Karger AG, Basel.

Arosio, B., Bulbarelli, A., Bastias Candia, S., Lonati, E., Mastronardi, L., Romualdi, P., et al. (2012). Pin1 contribution to Alzheimer's disease: Transcriptional and epigenetic mechanisms in patients with late-onset Alzheimer's disease. NEURODEGENERATIVE DISEASES, 10(1-4), 207-211 [10.1159/000333799].

Pin1 contribution to Alzheimer's disease: Transcriptional and epigenetic mechanisms in patients with late-onset Alzheimer's disease

BULBARELLI, ALESSANDRA;LONATI, ELENA RITA;
2012

Abstract

Background: Neurofibrillary tangles and senile plaques are hallmarks of Alzheimer's disease (AD) although the molecular basis of their coexistence remains elusive. The peptidyl-prolyl cis/trans isomerase Pin1 acts on both tau and amyloid precursor protein to regulate their functions by influencing tau phosphorylation and amyloid precursor protein processing. Objective: In order to identify potential biomarkers for AD in easily accessible cells and to gain insight into the relationship between the brain and peripheral compartments in AD pathology, we investigated Pin1 expression and activity in the peripheral blood mononuclear cells of subjects with late-onset AD (LOAD) and age-matched controls (CT). Methods: Gene and protein expression, promoter methylation, Ser 16 phosphorylation and activity of Pin1 were evaluated in 32 samples from subjects with LOAD and in 28 samples from CT. Results: In LOAD subjects, there was a statistically significant reduction in Ser 16 phosphorylation (-30%; p = 0.041) and promoter methylation (-8%; p = 0.001), whereas Pin1 expression was significantly increased (+74%; p = 0.018). Conclusion: The modifications of Pin1 found in LOAD subjects support its involvement in the pathogenesis of the disease with an important role being played by epigenetic mechanisms. Copyright © 2012 S. Karger AG, Basel.
Articolo in rivista - Articolo scientifico
Scientifica
Pin1, Alzheimer
English
Arosio, B., Bulbarelli, A., Bastias Candia, S., Lonati, E., Mastronardi, L., Romualdi, P., et al. (2012). Pin1 contribution to Alzheimer's disease: Transcriptional and epigenetic mechanisms in patients with late-onset Alzheimer's disease. NEURODEGENERATIVE DISEASES, 10(1-4), 207-211 [10.1159/000333799].
Arosio, B; Bulbarelli, A; Bastias Candia, S; Lonati, E; Mastronardi, L; Romualdi, P; Candeletti, S; Gussago, C; Galimberti, D; Scarpini, E; Dell'Osso, B; Altamura, C; Maccarrone, M; Bergamaschini, L; D'Addario, C; Mari, D
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/10281/44997
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