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Familial alzheimer’s disease lymphocytes respond differently than sporadic cells to oxidative stress: upregulated p53-p21 signaling linked with presenilin 1 mutants

AutorWojsiat, Joanna; Laskowska-Kaszub, Katarzyna; Alquézar, Carolina ; Bialopiotrowicz, Emilia; Esteras, Noemí ; Zdioruk, Mykola; Martín-Requero, Ángeles ; Wojda, Urszula
Palabras clave2-deoxy-D-ribose
Apoptosis
Familial Alzheimer’s disease
Lymphocytes
Mitochondrial membrane potential
Oxidative stress
Presenilin
Sporadic Alzheimer’s disease
p21
p53
Fecha de publicaciónsep-2017
EditorHumana Press
CitaciónMol Neurobiol. 54(7):5683-5698 (2017)
ResumenFamilial (FAD) and sporadic (SAD) Alzheimer's disease do not share all pathomechanisms, but knowledge on their molecular differences is limited. We previously reported that cell cycle control distinguishes lymphocytes from SAD and FAD patients. Significant differences were found in p21 levels of SAD compared to FAD lymphocytes. Since p21 can also regulate apoptosis, the aim of this study was to compare the response of FAD and SAD lymphocytes to oxidative stress like 2-deoxy-D-ribose (2dRib) treatment and to investigate the role of p21 levels in this response. We report that FAD cells bearing seven different PS1 mutations are more resistant to 2dRib-induced cell death than control or SAD cells: FAD cells showed a lower apoptosis rate and a lower depolarization of the mitochondrial membrane. Despite that basal p21 cellular content was lower in FAD than in SAD cells, in response to 2dRib, p21 mRNA and protein levels significantly increased in FAD cells. Moreover, we found a higher cytosolic accumulation of p21 in FAD cells. The transcriptional activation of p21 was shown to be dependent on p53, as it can be blocked by PFT-α, and correlated with the increased phosphorylation of p53 at Serine 15. Our results suggest that in FAD lymphocytes, the p53-mediated increase in p21 transcription, together with a shift in the nucleocytoplasmic localization of p21, confers a survival advantage against 2dRib-induced apoptosis. This compensatory mechanism is absent in SAD cells. Thus, therapeutic and diagnostic designs should take into account possible differential apoptotic responses in SAD versus FAD cells.
Descripción16 p.-7 fig.-2 tab.
Versión del editorhttp://dx.doi.org/10.1007/s12035-016-0105-y
URIhttp://hdl.handle.net/10261/154177
DOI10.1007/s12035-016-0105-y
ISSN0893-7648
E-ISSN1559-1182
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