Basic Science and Pathogenesis

Cheng, GWY; Ding, H; Tse, KH; Yoo, JS

Basic Science and Pathogenesis

Cheng, GWY Ding, H Tse, KH Yoo, JS

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Publisher:: Wiley
Publication Type:: Journal Article
Citation:: Alzheimer S Dementia the Journal of the Alzheimer S Association, 2025, 21, (Suppl 1), pp. e098988
Issue Date:: 2025-12-01

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Field	Value	Language
dc.contributor.author	Cheng, GWY
dc.contributor.author	Ding, H
dc.contributor.author	Tse, KH
dc.contributor.author	Yoo, JS
dc.date.accessioned	2026-02-10T08:53:22Z
dc.date.available	2026-02-10T08:53:22Z
dc.date.issued	2025-12-01
dc.identifier.citation	Alzheimer S Dementia the Journal of the Alzheimer S Association, 2025, 21, (Suppl 1), pp. e098988
dc.identifier.issn	1552-5260
dc.identifier.issn	1552-5279
dc.identifier.uri	http://hdl.handle.net/10453/193324
dc.description.abstract	BACKGROUND: Astrocytes are integral in maintaining tight junctions of the blood-brain barrier while supplying cholesterol to oligodendrocytes for myelination. It is well-recognized that vascular infarctions and white matter loss are signs of Alzheimer's disease (AD). Previously, we have shown that lipid-carrier apolipoprotein E isoform ε4 (ApoE4) was positively correlated with demyelination. Furthermore, oligodendrocyte loss and demyelination were shown to accelerate amyloid plaque deposition. However, the ApoE4 allele is not prevalent, only 25% are heterozygous and 3% homozygous, yet 95% of AD are sporadic. Thus, a novel AD pathway is necessary. Atherosclerosis is a condition in which plaques form in the inner linings of the vasculature, causing increased arterial pressure and risk of cerebral infarctions. The deposition of plaques prevents sufficient laminar shear stress, suppressing autophagy of the endothelial cells and, correspondingly, astrocytic autophagy. Consequently, the functions of astrocytes are hindered, one of which is its production and transport of cholesterol. Here, we hypothesize that atherosclerotic plaques would inhibit proper endothelial and astrocytic autophagy, resulting in improper cholesterol synthesis and transportation to oligodendrocytes and leading to demyelination. METHOD: In this study, we employed 7-month-old C57BL/6 controls (n = 6) with age-matched ApoE knockout mice (ApoeKO) (n = 6) to assess the impact of atherosclerosis on myelination. Quantitative analysis of white matter integrity was performed with T2-weighted and magnetic resonance spectroscopy sequences from Bruker BioSpec 70/20 USR7T. Y-maze and Promethion Metabolic Cage were used to investigate changes in short-term spatial memory and metabolic parameters, respectively. A battery of histochemistry was performed for quantitative assessments of atherosclerotic plaques, astrocytic and endothelial autophagy, myelination, and associated cell types. RESULT: Preliminary results show average respiration quotient of 0.94 for ApoeKO and 0.75 for control. We identified significant increase of Oil Red O lipid deposition in grey matter vasculature in ApoeKO indicative of atherosclerotic plaques. Immunohistochemistry shows a reduction in endothelial cell autophagy marker, TRIM47, in ApoeKO gross grey matter with no changes in astrocyte numbers. CONCLUSION: On-going confirmation of the impact of endothelial and astrocytic autophagy with myelination will elucidate underlying mechanisms of sporadic AD progression. Understanding the role of autophagy of astrocytes may highlight additional factors affecting neurodegenerative disorders.
dc.language	en
dc.publisher	Wiley
dc.relation.ispartof	Alzheimer S Dementia the Journal of the Alzheimer S Association
dc.relation.isbasedon	10.1002/alz70855_098988
dc.rights	info:eu-repo/semantics/openAccess
dc.subject	1103 Clinical Sciences, 1109 Neurosciences
dc.subject.classification	Geriatrics
dc.subject.classification	3202 Clinical sciences
dc.subject.classification	3209 Neurosciences
dc.subject.classification	5202 Biological psychology
dc.title	Basic Science and Pathogenesis
dc.type	Journal Article
utslib.citation.volume	21
utslib.for	1103 Clinical Sciences
utslib.for	1109 Neurosciences
pubs.organisational-group	University of Technology Sydney
pubs.organisational-group	University of Technology Sydney/Faculty of Science
pubs.organisational-group	University of Technology Sydney/Faculty of Science/School of Life Sciences
utslib.copyright.status	open_access	*
dc.rights.license	This work is licensed under a Creative Commons Attribution 4.0 International License (CC BY 4.0). To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/
dc.date.updated	2026-02-10T08:53:21Z
pubs.issue	Suppl 1
pubs.publication-status	Published
pubs.volume	21
utslib.citation.issue	Suppl 1

Abstract:

BACKGROUND: Astrocytes are integral in maintaining tight junctions of the blood-brain barrier while supplying cholesterol to oligodendrocytes for myelination. It is well-recognized that vascular infarctions and white matter loss are signs of Alzheimer's disease (AD). Previously, we have shown that lipid-carrier apolipoprotein E isoform ε4 (ApoE4) was positively correlated with demyelination. Furthermore, oligodendrocyte loss and demyelination were shown to accelerate amyloid plaque deposition. However, the ApoE4 allele is not prevalent, only 25% are heterozygous and 3% homozygous, yet 95% of AD are sporadic. Thus, a novel AD pathway is necessary. Atherosclerosis is a condition in which plaques form in the inner linings of the vasculature, causing increased arterial pressure and risk of cerebral infarctions. The deposition of plaques prevents sufficient laminar shear stress, suppressing autophagy of the endothelial cells and, correspondingly, astrocytic autophagy. Consequently, the functions of astrocytes are hindered, one of which is its production and transport of cholesterol. Here, we hypothesize that atherosclerotic plaques would inhibit proper endothelial and astrocytic autophagy, resulting in improper cholesterol synthesis and transportation to oligodendrocytes and leading to demyelination. METHOD: In this study, we employed 7-month-old C57BL/6 controls (n = 6) with age-matched ApoE knockout mice (ApoeKO) (n = 6) to assess the impact of atherosclerosis on myelination. Quantitative analysis of white matter integrity was performed with T2-weighted and magnetic resonance spectroscopy sequences from Bruker BioSpec 70/20 USR7T. Y-maze and Promethion Metabolic Cage were used to investigate changes in short-term spatial memory and metabolic parameters, respectively. A battery of histochemistry was performed for quantitative assessments of atherosclerotic plaques, astrocytic and endothelial autophagy, myelination, and associated cell types. RESULT: Preliminary results show average respiration quotient of 0.94 for ApoeKO and 0.75 for control. We identified significant increase of Oil Red O lipid deposition in grey matter vasculature in ApoeKO indicative of atherosclerotic plaques. Immunohistochemistry shows a reduction in endothelial cell autophagy marker, TRIM47, in ApoeKO gross grey matter with no changes in astrocyte numbers. CONCLUSION: On-going confirmation of the impact of endothelial and astrocytic autophagy with myelination will elucidate underlying mechanisms of sporadic AD progression. Understanding the role of autophagy of astrocytes may highlight additional factors affecting neurodegenerative disorders.

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http://hdl.handle.net/10453/193324