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Screening for Small Molecule Inhibitors of Statin-Induced APP C-terminal Toxic Fragment Production. | LitMetric

AI Article Synopsis

  • Alzheimer's disease (AD) involves the loss of neurons and synapses, potentially linked to the cleavage of the amyloid precursor protein (APP), which produces a toxic peptide (APP-C31) and a truncated form of APP (APPΔC31).
  • A study suggests that blocking this caspase cleavage through specific mutations can reduce synaptic loss and cognitive issues in mice with AD, indicating it as a promising target for new treatments.
  • Researchers used specialized antibodies and screening methods to identify small molecules that inhibit the production of APP-C31 and discovered several compounds that can prevent APPΔC31 production and cell death in lab models, paving the way for further tests in AD mouse models.

Article Abstract

Alzheimer's disease (AD) is characterized by neuronal and synaptic loss. One process that could contribute to this loss is the intracellular caspase cleavage of the amyloid precursor protein (APP) resulting in release of the toxic C-terminal 31-amino acid peptide APP-C31 along with the production of APPΔC31, full-length APP minus the C-terminal 31 amino acids. We previously found that a mutation in APP that prevents this caspase cleavage ameliorated synaptic loss and cognitive impairment in a murine AD model. Thus, inhibition of this cleavage is a reasonable target for new therapeutic development. In order to identify small molecules that inhibit the generation of APP-C31, we first used an APPΔC31 cleavage site-specific antibody to develop an AlphaLISA to screen several chemical compound libraries for the level of N-terminal fragment production. This antibody was also used to develop an ELISA for validation studies. In both high throughput screening (HTS) and validation testing, the ability of compounds to inhibit simvastatin- (HTS) or cerivastatin- (validation studies) induced caspase cleavage at the APP-D720 cleavage site was determined in Chinese hamster ovary (CHO) cells stably transfected with wildtype (wt) human APP (CHO-7W). Several compounds, as well as control pan-caspase inhibitor Q-VD-OPh, inhibited APPΔC31 production (measured fragment) and rescued cell death in a dose-dependent manner. The effective compounds fell into several classes including SERCA inhibitors, inhibitors of Wnt signaling, and calcium channel antagonists. Further studies are underway to evaluate the efficacy of lead compounds - identified here using cells and tissues expressing wt human APP - in mouse models of AD expressing mutated human APP, as well as to identify additional compounds and determine the mechanisms by which they exert their effects.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5309220PMC
http://dx.doi.org/10.3389/fphar.2017.00046DOI Listing

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