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Journal ArticleOpen Access

The human-specific<i>CASP4</i>gene product contributes to Alzheimer-related synaptic and behavioural deficits

Author Affiliations
Icahn School of Medicine at Mount Sinai, Directorate General of Health Services, James J. Peters VA Medical Center, Allen Institute for Brain Science, ...
Published InHuman Molecular Genetics
Year2016
Citations37

Abstract

Recent studies have indicated that innate immune signalling molecules are involved in late-onset Alzheimer's disease (LOAD) risk. Amyloid beta (Aβ) accumulates in AD brain, and has been proposed to act as a trigger of innate immune responses. Caspase-4 is an important part of the innate immune response. We recently characterized transgenic mice carrying human CASP4, and observed that the mice manifested profound innate immune responses to lipopolysaccharide (LPS). Since these inflammatory processes are important in the aetiology of AD, we have now analysed the correlation of expression of caspase-4 in human brain with AD risk genes, and studied caspase-4 effects on AD-related phenotypes in APPswe/PS1deltaE9 (APP/PS1) mice. We observed that the expression of caspase-4 was strongly correlated with AD risk…
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