Three-dimensional real time imaging of amyloid β aggregation on living cells

被引:18
|
作者
Kuragano, Masahiro [1 ]
Yamashita, Ryota [1 ]
Chikai, Yusaku [1 ]
Kitamura, Ryota [1 ]
Tokuraku, Kiyotaka [1 ]
机构
[1] Muroran Inst Technol, Grad Sch Engn, 27-1 Mizumoto, Muroran, Hokkaido 0508585, Japan
关键词
DENDRITIC SPINES; PROTEIN FIBRILLOGENESIS; ALZHEIMERS-DISEASE; SMALL GTPASES; IN-VITRO; PLASTICITY; PLAQUES; RHO; POTENTIATION; FIBRILLATION;
D O I
10.1038/s41598-020-66129-z
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Alzheimer's disease (AD) is a progressive disorder of the brain that gradually decreases thinking, memory, and language abilities. The aggregation process of amyloid beta (A beta) is a key step in the expression of its neurocytotoxicity and development of AD because A beta aggregation and accumulation around neuronal cells induces cell death. However, the molecular mechanism underlying the neurocytotoxicity and cell death by A beta aggregation has not been clearly elucidated. In this study, we successfully visualized real-time process of A beta(42) aggregation around living cells by applying our established QD imaging method. 3D observations using confocal laser microscopy revealed that A beta(42) preferentially started to aggregate at the region where membrane protrusions frequently formed. Furthermore, we found that inhibition of actin polymerization using cytochalasin D reduced aggregation of A beta(42) on the cell surface. These results indicate that actin polymerization-dependent cell motility is responsible for the promotion of A beta(42) aggregation at the cell periphery. 3D observation also revealed that the aggregates around the cell remained in that location even if cell death occurred, implying that amyloid plaques found in the AD brain grew from the debris of dead cells that accumulated A beta(42) aggregates.
引用
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页数:12
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