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Aß-Aggregation-Generated Blue Autofluorescence Illuminates Senile Plaques as well as Complex Blood and Vascular Pathologies in Alzheimer's Disease.
Fu, Hualin; Li, Jilong; Zhang, Chunlei; Du, Peng; Gao, Guo; Ge, Qiqi; Guan, Xinping; Cui, Daxiang.
Affiliation
  • Fu H; Institute of Nano Biomedicine and Engineering, School of Sensing Science and Engineering, School of Electronic Information and Electrical Engineering, Shanghai Jiao Tong University, Shanghai, 200240, China. hfu@sjtu.edu.cn.
  • Li J; Institute of Marine Equipment, Shanghai Jiao Tong University, Shanghai, 200240, China. hfu@sjtu.edu.cn.
  • Zhang C; National Center for Translational Medicine, Shanghai Jiao Tong University, Shanghai, 200240, China. hfu@sjtu.edu.cn.
  • Du P; Institute of Nano Biomedicine and Engineering, School of Sensing Science and Engineering, School of Electronic Information and Electrical Engineering, Shanghai Jiao Tong University, Shanghai, 200240, China.
  • Gao G; Institute of Nano Biomedicine and Engineering, School of Sensing Science and Engineering, School of Electronic Information and Electrical Engineering, Shanghai Jiao Tong University, Shanghai, 200240, China.
  • Ge Q; National Center for Translational Medicine, Shanghai Jiao Tong University, Shanghai, 200240, China.
  • Guan X; Department of Colorectal Surgery, School of Medicine, Xinhua Hospital, Shanghai Jiao Tong University, Shanghai, 200092, China.
  • Cui D; Institute of Nano Biomedicine and Engineering, School of Sensing Science and Engineering, School of Electronic Information and Electrical Engineering, Shanghai Jiao Tong University, Shanghai, 200240, China.
Neurosci Bull ; 40(8): 1115-1126, 2024 Aug.
Article in En | MEDLINE | ID: mdl-38345691
ABSTRACT
Senile plaque blue autofluorescence was discovered around 40 years ago, however, its impact on Alzheimer's disease (AD) pathology has not been fully examined. We analyzed senile plaques with immunohistochemistry and fluorescence imaging on AD brain sections and also Aß aggregation in vitro. In DAPI or Hoechst staining, the nuclear blue fluorescence could only be correctly assigned after subtracting the blue plaque autofluorescence. The flower-like structures wrapping dense-core blue fluorescence formed by cathepsin D staining could not be considered central-nucleated neurons with defective lysosomes since there was no nuclear staining in the plaque core when the blue autofluorescence was subtracted. Both Aß self-oligomers and Aß/hemoglobin heterocomplexes generated blue autofluorescence. The Aß amyloid blue autofluorescence not only labels senile plaques but also illustrates red cell aggregation, hemolysis, cerebral amyloid angiopathy, vascular plaques, vascular adhesions, and microaneurysms. In summary, we conclude that Aß-aggregation-generated blue autofluorescence is an excellent multi-amyloidosis marker in Alzheimer's disease.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Amyloid beta-Peptides / Plaque, Amyloid / Alzheimer Disease Limits: Aged / Aged80 / Female / Humans / Male Language: En Journal: Neurosci Bull / Neurosci. bull / Neuroscience bulletin Journal subject: NEUROLOGIA Year: 2024 Document type: Article Affiliation country: China Country of publication: Singapore

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Amyloid beta-Peptides / Plaque, Amyloid / Alzheimer Disease Limits: Aged / Aged80 / Female / Humans / Male Language: En Journal: Neurosci Bull / Neurosci. bull / Neuroscience bulletin Journal subject: NEUROLOGIA Year: 2024 Document type: Article Affiliation country: China Country of publication: Singapore