Receptor for Advanced Glycation End Products (RAGE) is Expressed Predominantly in Medium Spiny Neurons of tgHD Rat Striatum.

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dc.contributor.author Shi, Dian
dc.contributor.author Chang, Joshua W
dc.contributor.author Choi, Jaimin
dc.contributor.author Connor, Bronwen
dc.contributor.author O'Carroll, Simon J
dc.contributor.author Nicholson, Louise FB
dc.contributor.author Kim, Joo Hyun
dc.coverage.spatial United States
dc.date.accessioned 2021-11-11T22:42:52Z
dc.date.available 2021-11-11T22:42:52Z
dc.date.issued 2018-6
dc.identifier.issn 0306-4522
dc.identifier.uri https://hdl.handle.net/2292/57405
dc.description.abstract Receptor for advanced glycation end products (RAGE) is a multi-ligand receptor involved in the pathology of several progressive neurodegenerative disorders including Huntington's disease (HD). We previously showed that the expression of RAGE and its colocalization with ligands were increased in the striatum of HD patients, increasing with grade severity, and that the pattern of RAGE expression coincided with the medio-lateral pattern of neurodegeneration. However, the exact role of RAGE in HD remains elusive. In order to address the necessity for a direct functional study, we aimed to characterize the pattern of RAGE expression in the transgenic rat model of HD (tgHD rats). Our results showed that RAGE expression was expanded laterally in tgHD rat caudate-putamen (CPu) compared to wildtype littermates, but the expression was unchanged by disease severity. The rostro-caudal location did not affect RAGE expression. RAGE was predominantly expressed in the medium spiny neurons (MSN) where it colocalized most extensively with N-carboxymethyllysine (CML), which largely contradicts with observations from human HD brains. Overall, the tgHD rat model only partially recapitulated the pattern in striatal RAGE expression in human brains, raising a question about its reliability as an animal model for future functional studies.
dc.format.medium Print-Electronic
dc.language eng
dc.publisher Elsevier BV
dc.relation.ispartofseries Neuroscience
dc.rights Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. Previously published items are made available in accordance with the copyright policy of the publisher.
dc.rights.uri https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm
dc.subject Corpus Striatum
dc.subject Neurons
dc.subject Animals
dc.subject Rats
dc.subject Huntington Disease
dc.subject Disease Models, Animal
dc.subject Female
dc.subject Rats, Transgenic
dc.subject Receptor for Advanced Glycation End Products
dc.subject Huntington’s disease
dc.subject N-carboxymethyllysine
dc.subject S100B
dc.subject receptor for advanced glycation end products
dc.subject tgHD rats
dc.subject Animals
dc.subject Corpus Striatum
dc.subject Disease Models, Animal
dc.subject Female
dc.subject Huntington Disease
dc.subject Neurons
dc.subject Rats
dc.subject Rats, Transgenic
dc.subject Receptor for Advanced Glycation End Products
dc.subject Science & Technology
dc.subject Life Sciences & Biomedicine
dc.subject Neurosciences
dc.subject Neurosciences & Neurology
dc.subject receptor for advanced glycation end products
dc.subject N-carboxymethyllysine
dc.subject S100B
dc.subject Huntington's disease
dc.subject tgHD rats
dc.subject HUNTINGTONS-DISEASE
dc.subject MODEL
dc.subject NEUROPATHOLOGY
dc.subject 1109 Neurosciences
dc.subject Biomedical
dc.subject Basic Science
dc.subject Neurodegenerative
dc.subject Huntington's Disease
dc.subject Neurosciences
dc.subject Rare Diseases
dc.subject Brain Disorders
dc.subject Neurological
dc.subject 2.1 Biological and endogenous factors
dc.subject 1109 Neurosciences
dc.subject 1701 Psychology
dc.subject 1702 Cognitive Sciences
dc.title Receptor for Advanced Glycation End Products (RAGE) is Expressed Predominantly in Medium Spiny Neurons of tgHD Rat Striatum.
dc.type Journal Article
dc.identifier.doi 10.1016/j.neuroscience.2018.03.042
pubs.begin-page 146
pubs.volume 380
dc.date.updated 2021-10-15T01:28:21Z
dc.rights.holder Copyright: The author en
pubs.author-url https://www.ncbi.nlm.nih.gov/pubmed/29625216
pubs.end-page 151
pubs.publication-status Published
dc.rights.accessrights http://purl.org/eprint/accessRights/RestrictedAccess en
pubs.subtype Research Support, Non-U.S. Gov't
pubs.subtype Journal Article
pubs.elements-id 735718
dc.identifier.eissn 1873-7544
dc.identifier.pii S0306-4522(18)30240-9


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