期刊
FEBS LETTERS
卷 587, 期 13, 页码 2046-2054出版社
WILEY
DOI: 10.1016/j.febslet.2013.05.010
关键词
Amyloid precursor protein; APP intracellular domain (AICD); Histone deacetylase; Hypoxia; Mediator; Neprilysin
资金
- UK Medical Research Council [G0501565, G0802189]
- Alzheimer's Research UK [ART/PhD2009/4, ARUK-ESG2012-1]
- RFBR
- Program RAS Fundamental Science to Medicine
- Alzheimers Research UK [ARUK-ESG2013-1] Funding Source: researchfish
- Medical Research Council [G0501565, G0802189] Funding Source: researchfish
- MRC [G0501565, G0802189] Funding Source: UKRI
For 20 years the amyloid cascade hypothesis of Alzheimer disease (AD) has placed the amyloid-beta peptide (A beta), formed from the amyloid precursor protein (APP), centre stage in the process of neurodegeneration. However, no new therapeutic agents have reached the clinic through exploitation of the hypothesis. The APP metabolites, including A beta, generated by its proteolytic processing, have distinct physiological functions. In particular, the cleaved intracellular domain of APP (AICD) regulates expression of several genes, including APP itself, the beta-secretase BACE-1 and the A beta-degrading enzyme, neprilysin and this transcriptional regulation involves direct promoter binding of AICD. Of the three major splice isoforms of APP (APP(695), APP(751), APP(770)), APP(695) is the predominant neuronal form, from which A beta and transcriptionally-active AICD are preferentially generated by selective processing through the amyloidogenic pathway. Despite intensive research, the normal functions of the APP isoforms remain an enigma. APP plays an important role in brain development, memory and synaptic plasticity and secreted forms of APP are neuroprotective. A fuller understanding of the physiological and pathological actions of APP and its metabolic and gene regulatory network could provide new therapeutic opportunities in neurodegeneration, including AD. (c) 2013 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
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