Live Cell FRET Imaging Reveals Amyloid β-Peptide Oligomerization in Hippocampal Neurons

被引:4
|
作者
Gao, Yang [1 ]
Wennmalm, Stefan [2 ]
Winblad, Bengt [1 ,3 ]
Schedin-Weiss, Sophia [1 ]
Tjernberg, Lars O. [1 ]
机构
[1] Karolinska Inst, Dept Neurobiol Care Sci & Soc, Div Neurogeriatr, S-17164 Solna, Sweden
[2] Royal Inst Technol, Dept Appl Phys, SciLifeLab, Biophys, S-17165 Solna, Sweden
[3] Karolinska Univ Hosp, Theme Inflammat & Aging, S-14186 Huddinge, Sweden
基金
瑞典研究理事会;
关键词
amyloid β -peptide; oligomerization; aggregation; FRET; PROTEIN; PATHOGENESIS; AGGREGATION;
D O I
10.3390/ijms22094530
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Amyloid beta-peptide (A beta) oligomerization is believed to contribute to the neuronal dysfunction in Alzheimer disease (AD). Despite decades of research, many details of A beta oligomerization in neurons still need to be revealed. Forster resonance energy transfer (FRET) is a simple but effective way to study molecular interactions. Here, we used a confocal microscope with a sensitive Airyscan detector for FRET detection. By live cell FRET imaging, we detected A beta 42 oligomerization in primary neurons. The neurons were incubated with fluorescently labeled A beta 42 in the cell culture medium for 24 h. A beta 42 were internalized and oligomerized in the lysosomes/late endosomes in a concentration-dependent manner. Both the cellular uptake and intracellular oligomerization of A beta 42 were significantly higher than for A beta 40. These findings provide a better understanding of A beta 42 oligomerization in neurons.
引用
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页数:11
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