Preservation of cell survival mechanisms by the presenilin-1 K239N mutation may cause its milder clinical phenotype

Publication date: Available online 15 July 2016
Source:Neurobiology of Aging
Author(s): Sara Sarroca, Patricia Molina-Martínez, Cristina Aresté, Martin Etzrodt, Pablo García de Frutos, Rosa Gasa, Anna Antonell, José Luís Molinuevo, Raquel Sánchez-Valle, Carlos A. Saura, Albert Lladó, Coral Sanfeliu
Presenilin 1 (PSEN1) mutations are the main cause of monogenic Alzheimer's disease (AD). We studied the functional effects of the mutation K239N, which shows incomplete penetrance at the age of 65 years, and compared it with the more aggressive mutation E120G. We engineered stable cell lines expressing human PSEN1 wild-type or with K239N or E120G mutations. Both mutations induced dysfunction of γ-secretase in the processing of AβPP, leading to an increase in the Aβ42/Aβ40 ratio. Analysis of homeostatic mechanisms showed that K239N induced lower basal and hydrogen peroxide-induced intracellular levels of reactive oxygen species than E120G. Similarly, K239N induced lower vulnerability to apoptosis by hydrogen peroxide injury than E120G. Accordingly, the proapoptotic signaling pathways JNK and p38 MAPK maintained PSEN1-mediated negative regulation in K239N, but not in E120G-bearing cells. Furthermore, the activation of the prosurvival signaling pathways MAPK/ERK and PI3K/Akt was lower in E120G-bearing cells. Therefore, preservation of mechanisms regulating cell responses independently of AβPP processing may account for the milder phenotype induced by the PSEN1 K239N mutation.



from #ORL via xlomafota13 on Inoreader http://ift.tt/2a1rHUr
via IFTTT