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J Alzheimers Dis ; 62(1): 175-202, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-29439343

RESUMO

The BRCA1 protein, one of the major players responsible for DNA damage response has recently been linked to Alzheimer's disease (AD). Using primary fibroblasts and neurons reprogrammed from induced pluripotent stem cells (iPSC) derived from familial AD (FAD) patients, we studied the role of the BRCA1 protein underlying molecular neurodegeneration. By whole-transcriptome approach, we have found wide range of disturbances in cell cycle and DNA damage response in FAD fibroblasts. This was manifested by significantly increased content of BRCA1 phosphorylated on Ser1524 and abnormal ubiquitination and subcellular distribution of presenilin 1 (PS1). Accordingly, the iPSC-derived FAD neurons showed increased content of BRCA1(Ser1524) colocalized with degraded PS1, accompanied by an enhanced immunostaining pattern of amyloid-ß. Finally, overactivation of BRCA1 was followed by an increased content of Cdc25C phosphorylated on Ser216, likely triggering cell cycle re-entry in FAD neurons. This study suggests that overactivated BRCA1 could both influence PS1 turnover leading to amyloid-ß pathology and promote cell cycle re-entry-driven cell death of postmitotic neurons in AD.


Assuntos
Doença de Alzheimer/metabolismo , Proteína BRCA1/metabolismo , Células-Tronco Pluripotentes Induzidas/metabolismo , Degeneração Neural/metabolismo , Neurônios/metabolismo , Presenilina-1/metabolismo , Doença de Alzheimer/genética , Doença de Alzheimer/patologia , Peptídeos beta-Amiloides/metabolismo , Células Cultivadas , Técnicas de Reprogramação Celular , Biologia Computacional , Fibroblastos/metabolismo , Fibroblastos/patologia , Expressão Gênica , Humanos , Degeneração Neural/genética , Degeneração Neural/patologia , Neurônios/patologia , Fosforilação , Presenilina-1/genética , Presenilina-2/genética , Presenilina-2/metabolismo , Transdução de Sinais , Transcriptoma , Fosfatases cdc25/metabolismo
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