TY - JOUR
T1 - Gelsolin Encountering Ag Nanorods/Triangles
T2 - An Aggregation-Based Colorimetric Sensor Array for in Vivo Monitoring the Cerebrospinal Aβ42% as an Indicator of Cd2+Exposure-Related Alzheimer's Disease Pathogenesis
AU - Liu, Chang
AU - You, Xinrui
AU - Lu, Dingkun
AU - Shi, Guoyue
AU - Deng, Jingjing
AU - Zhou, Tianshu
N1 - Publisher Copyright:
© 2020 American Chemical Society.
PY - 2020/11/16
Y1 - 2020/11/16
N2 - Nowadays, the environmental risk factors for Alzheimer's disease (AD) have received widespread attention. Two major amyloid-β peptide (Aβ) variants, Aβ42 and Aβ40, play a pivotal role in the etiology of AD and the concentration ratio of which (i.e., Aβ42%) has been suggested to be the superior biomarker for AD. In this study, an "aggregation-based colorimetric sensor array"for the simultaneous identification and detection of Aβ40 and Aβ42 with structural similarity was established based on gelsolin-modified silver nanotriangles (Ag NTs) and silver nanorods (Ag NRs). Different aggregation behaviors of gelsolin-modified Ag NTs and Ag NRs in the presence of Aβ42 and Aβ40 resulted in different color and spectral changes, which could be quantitatively analyzed in terms of unique spectral patterns by principal component analysis. With the colorimetric sensor array employed here, the fluctuation of Aβ42% in different brain regions of rats exposed to Cd2+ could be directly monitored. The downward trend of Aβ42% accompanied by variations of other biochemical indicators suggested that subchronic Cd2+ exposure possibly triggered the onset of AD through the intervention of lipid peroxidation pathway. Furthermore, in vivo monitoring the downtrend of Aβ42% in cerebrospinal fluid (CSF) could also be realized, which offers a great opportunity for early diagnosis and treatment of AD that may be induced by environmental factors with CSF Aβ42% as a reliable indicator.
AB - Nowadays, the environmental risk factors for Alzheimer's disease (AD) have received widespread attention. Two major amyloid-β peptide (Aβ) variants, Aβ42 and Aβ40, play a pivotal role in the etiology of AD and the concentration ratio of which (i.e., Aβ42%) has been suggested to be the superior biomarker for AD. In this study, an "aggregation-based colorimetric sensor array"for the simultaneous identification and detection of Aβ40 and Aβ42 with structural similarity was established based on gelsolin-modified silver nanotriangles (Ag NTs) and silver nanorods (Ag NRs). Different aggregation behaviors of gelsolin-modified Ag NTs and Ag NRs in the presence of Aβ42 and Aβ40 resulted in different color and spectral changes, which could be quantitatively analyzed in terms of unique spectral patterns by principal component analysis. With the colorimetric sensor array employed here, the fluctuation of Aβ42% in different brain regions of rats exposed to Cd2+ could be directly monitored. The downward trend of Aβ42% accompanied by variations of other biochemical indicators suggested that subchronic Cd2+ exposure possibly triggered the onset of AD through the intervention of lipid peroxidation pathway. Furthermore, in vivo monitoring the downtrend of Aβ42% in cerebrospinal fluid (CSF) could also be realized, which offers a great opportunity for early diagnosis and treatment of AD that may be induced by environmental factors with CSF Aβ42% as a reliable indicator.
KW - AD pathogenesis
KW - Cdexposure
KW - cerebrospinal Aβpercent
KW - colorimetric sensor array
KW - gelsolin-modified Ag nanorods/triangles
UR - https://www.scopus.com/pages/publications/85096015926
U2 - 10.1021/acsabm.0c01078
DO - 10.1021/acsabm.0c01078
M3 - 文章
AN - SCOPUS:85096015926
SN - 2576-6422
VL - 3
SP - 7965
EP - 7973
JO - ACS Applied Bio Materials
JF - ACS Applied Bio Materials
IS - 11
ER -