• Dian Shi, Joshua W Chang, Jaimin Choi, Bronwen Connor, Simon J O'Carroll, Nicholson Louise F B LFB Department of Anatomy and Medical Imaging, and the Centre for Brain Research, Faculty of Medical and Health Sciences, University of Auckland, 85 , and Joo Hyun Kim.
• Department of Anatomy and Medical Imaging, and the Centre for Brain Research, Faculty of Medical and Health Sciences, University of Auckland, 85 Park Rd, Grafton, Auckland 1142, New Zealand.
• Neuroscience. 2018 Jun 1; 380: 146-151.

AbstractReceptor 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.Copyright © 2018 IBRO. Published by Elsevier Ltd. All rights reserved.

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