期刊
JOURNAL OF NEUROSCIENCE
卷 34, 期 7, 页码 2464-2470出版社
SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.0151-13.2014
关键词
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资金
- National Institutes of Health [R01NS054880, R01AG031893, R21AG041934, R01AG021173, R01NS046673, R01AG030197, R01AG038710, R03AG034366]
- Alzheimer's Association [IIRG-11-204030]
The excessive accumulation of soluble amyloid peptides (A beta) plays a crucial role in the pathogenesis of Alzheimer's disease (AD), particularly in synaptic dysfunction. The role of the two major chaperone proteins, Hsp70 and Hsp90, in clearing misfolded protein aggregates has been established. Despite their abundant presence in synapses, the role of these chaperones in synapses remains elusive. Here, we report that Hsp90 inhibition by 17-AAG elicited not only a heat shock-like response but also upregulated presynaptic and postsynaptic proteins, such as synapsin I, synaptophysin, and PSD95 in neurons. 17-AAG treatment enhanced high-frequency stimulation-evoked LTP and protected neurons from synaptic damage induced by soluble A beta. In AD transgenic mice, the daily administration of 17-AAG over 7 d resulted in a marked increase in PSD95 expression in hippocampi. 17-AAG treatments in wild-type C57BL/6 mice challenged by soluble A beta significantly improved contextual fear memory. Further, we demonstrate that 17-AAG activated synaptic protein expression via transcriptional mechanisms through the heat shock transcription factor HSF1. Together, our findings identify a novel function of Hsp90 inhibition in regulating synaptic plasticity, in addition to the known neuroprotective effects of the chaperones against A beta and tau toxicity, thus further supporting the potential of Hsp90 inhibitors in treating neurodegenerative diseases.
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