@article{f53ca6cf6d094887840b79927d42cf4f,
title = "Increased glutaminyl cyclase activity in brains of Alzheimer's disease individuals",
abstract = "Glutaminyl cyclases (QC) catalyze the formation of neurotoxic pGlu-modified amyloid-β peptides found in the brains of people with Alzheimer's disease (AD). Reports of several-fold increases in soluble QC (sQC) expression in the brain and peripheral circulation of AD individuals has prompted the development of QC inhibitors as potential AD therapeutics. There is, however, a lack of standardized quantitative data on QC expression in human tissues, precluding inter-laboratory comparison and validation. We tested the hypothesis that QC is elevated in AD tissues by quantifying levels of sQC protein and activity in post-mortem brain tissues from AD and age-matched control individuals. We found a modest but statistically significant increase in sQC protein, which paralleled a similar increase in enzyme activity. In plasma samples sourced from the Australian Imaging, Biomarker and Lifestyle study we determined that QC activity was not different between the AD and control group, though a modest increase was observed in female AD individuals compared to controls. Plasma QC activity was further correlated with levels of circulating monocytes in AD individuals. These data provide quantitative evidence that alterations in QC expression are associated with AD pathology. (Figure presented.).",
keywords = "Alzheimer's disease, amyloid-beta, glutaminyl cyclase, monocyte, pyroglutamate, amyloid-β",
author = "Gunn, {Adam P.} and Wong, {Bruce X.} and Catriona McLean and Chris Fowler and Barnard, {Peter J.} and Duce, {James A.} and Roberts, {Blaine R.}",
note = "Funding Information: APG would like to acknowledge project support and guidance from Ashley I. Bush and Robert A. Cherny (FINMH, University of Melbourne, Australia). We would like to acknowledge the volunteers and their families and the Australian Imaging and Biomarker, Lifestyle (AIBL) research team (http:/// www.aible.csiro.au ). Tissues were received from the Victorian Brain Bank, supported by the University of Melbourne, Alfred Hospital, the Victorian Forensic Institute of Medicine, and the National Health and Medical Research Council. We acknowledge funding from the Victorian Government's Operational Infrastructure Support Program. Partial support from the Australian Research Council Linkage Projects Scheme (with Agilent Technologies), the Cooperative Research Centre for Mental Health, and the Alzheimer's Drug Discovery Research Foundation. BR is a National Health and Medical Research Council Dementia leadership fellow (grant ID APP1138673) with NHMRC project grant (ID: APP1164692). BR receives financial support from Agilent Technologies (Mulgrave, Victoria) and research support from Agilent Technologies, Biosensis (Adelaide, South Australia) and eMSion (Corvallis, Oregon). Publisher Copyright: {\textcopyright} 2020 International Society for Neurochemistry",
year = "2021",
month = mar,
doi = "10.1111/jnc.15114",
language = "English",
volume = "156",
pages = "979--987",
journal = "Journal of Neurochemistry",
issn = "0022-3042",
publisher = "Wiley-Blackwell",
number = "6",
}