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Circadian control of heparan sulfate levels times phagocytosis of amyloid beta aggregates.


ABSTRACT: 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.

SUBMITTER: Clark GT 

PROVIDER: S-EPMC8830681 | biostudies-literature | 2022 Feb

REPOSITORIES: biostudies-literature

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Circadian control of heparan sulfate levels times phagocytosis of amyloid beta aggregates.

Clark Gretchen T GT   Yu Yanlei Y   Urban Cooper A CA   Fu Guo G   Wang Chunyu C   Zhang Fuming F   Linhardt Robert J RJ   Hurley Jennifer M JM  

PLoS genetics 20220210 2


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 lin  ...[more]

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