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• W1997945031 abstract "Recent studies have indicated that prolonged dysfunction and/or stress in the endoplasmic reticulum (ER) may contribute to pathogenesis and neurodegeneration. The disorder caused by misfolding and aggregation of proteins has been referred to as conformational disease, including Alzheimer's disease (AD). AD is characterized by the accumulation of extracellular amyloid-beta1-42 (A beta 42) fibrils with reactive microglia. Understanding the balance of production and clearance of A beta 42 is the key to elucidating amyloid plaque homeostasis. We have recently found that microglial phagocytosis of A beta 42 may be essentially driven by dynamic reorganization of the actin cytoskeleton through the pathway of WAVE and Rac1. In addition, an extracellular stress protein, such as Hsp90, enhances A beta 42 phagocytosis. HMGB1 inhibits microglial phagocytosis of A beta 42, and it binds A beta 42 and stabilizes the oligomerization. These results suggest that microglial clearance of A beta 42 may be another option for investigations in the search for a therapeutic strategy for AD, in addition to the study of production and degradation of A beta 42." @default.
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• W1997945031 date "2004-01-01" @default.
• W1997945031 modified "2023-09-27" @default.
• W1997945031 title "Stress proteins and regulation of microglial amyloid-β phagocytosis" @default.
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• W1997945031 doi "https://doi.org/10.1254/fpj.124.407" @default.
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