期刊
JOURNAL OF BIOLOGICAL CHEMISTRY
卷 285, 期 24, 页码 18344-18351出版社
AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.M110.112664
关键词
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资金
- National Research Council (CNR) [DG.RSTL.059.012]
- Compagnia di San Paolo-Programma Neuroscienze
- REGIONE LAZIO
The amyloid precursor protein (APP) and its proteolytic product amyloid beta (A beta) are associated with both familial and sporadic forms of Alzheimer disease (AD). Aberrant expression and function of microRNAs has been observed in AD. Here, we show that in rat hippocampal neurons cultured in vitro, the down-regulation of Argonaute-2, a key component of the RNA-induced silencing complex, produced an increase in APP levels. Using site-directed mutagenesis, a microRNA responsive element (RE) for miR-101 was identified in the 3'-untranslated region (UTR) of APP. The inhibition of endogenous miR-101 increased APP levels, whereas lentiviral-mediated miR-101 overexpression significantly reduced APP and A beta load in hippocampal neurons. In addition, miR-101 contributed to the regulation of APP in response to the proinflammatory cytokine interleukin-1 beta (IL-1 beta). Thus, miR-101 is a negative regulator of APP expression and affects the accumulation of A beta, suggesting a possible role for miR-101 in neuropathological conditions.
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