Circadian Control of Heparan Sulfate Levels Times Phagocytosis of Amyloid Beta Aggregates
Author
Clark, Gretchen T.; Yu, Yanlei; Urban, Cooper A.; Fu, Guo; Wang, Chunyu; Zhang, Fuming; Linhardt, Robert J.; Hurley, Jennifer M.
Other Contributors
Date Issued
2022-02-10Subject
Biology; Chemistry and chemical biology; Chemical and biological engineering; Biomedical engineeringDegree
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In Copyright : this Item is protected by copyright and/or related rights. You are free to use this Item in any way that is permitted by the copyright and related rights legislation that applies to your use. For other uses you need to obtain permission from the rights-holder(s). https://rightsstatements.org/page/InC/1.0/; Attribution 3.0 United StatesFull Citation
Circadian Control of Heparan Sulfate Levels Times Phagocytosis of Amyloid Beta Aggregates. G. T. Clark, Y. Yu, C. A. Urban, G. Fu, C. Wang, F. Zhang, R. J. Linhardt, J. M. Hurley, PLOS Genetics, 18(2): e1009994, 2022.Metadata
Show full item recordAbstract
Alzheimer’s Disease (AD) is a neuroinflammatory disease characterized partly by the inability to clear, and subsequent build-up, of amyloid-beta (Aβ). AD has a bi-directional relationship with circadian disruption (CD) with sleep disturbances starting years before disease onset. However, the molecular mechanism underlying the relationship of CD and AD has not been elucidated. Myeloid-based phagocytosis, a key component in the metabolism of Aβ, is circadianly-regulated, presenting a potential link between CD and AD. In this work, we revealed that the phagocytosis of Aβ42 undergoes a daily circadian oscillation. We found the circadian timing of global heparan sulfate proteoglycan (HSPG) biosynthesis was the molecular timer for the clock-controlled phagocytosis of Aβ and that both HSPG binding and aggregation may play a role in this oscillation. These data highlight that circadian regulation in immune cells may play a role in the intricate relationship between the circadian clock and AD.;Description
PLOS Genetics, 18(2): e1009994; Note : if this item contains full text it may be a preprint, author manuscript, or a Gold OA copy that permits redistribution with a license such as CC BY. The final version is available through the publisher’s platform.Department
The Linhardt Research Labs.; The Shirley Ann Jackson, Ph.D. Center for Biotechnology and Interdisciplinary Studies (CBIS);Publisher
Public Library of Science (PLoS)Relationships
The Linhardt Research Labs Online Collection; Rensselaer Polytechnic Institute, Troy, NY; PLoS Genetics; https://harc.rpi.edu/;Access
CC BY — Creative Commons Attribution; A full text version is available in DSpace@RPI; Open Access;Collections
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