Natural Compound from Olive Oil Inhibits S100A9 Amyloid Formation and Cytotoxicity: Implications for Preventing Alzheimer's Disease

被引:24
|
作者
Leri, Manuela [1 ,2 ]
Chaudhary, Himanshu [3 ]
Iashchishyn, Igor A. [3 ]
Pansieri, Jonathan [3 ]
Svedruzic, Zeljko M. [4 ]
Alcalde, Silvia Gomez [3 ]
Musteikyte, Greta [5 ]
Smirnovas, Vytautas [5 ]
Stefani, Massimo [1 ]
Bucciantini, Monica [1 ]
Morozova-Roche, Ludmilla A. [3 ]
机构
[1] Univ Florence, Dept Expt & Clin Biomed Sci Mario Serio, I-50134 Florence, Italy
[2] Univ Florence, Dept Neurosci Psychol Drug Res & Child Hlth, I-50139 Florence, Italy
[3] Umea Univ, Dept Med Biochem & Biophys, S-90187 Umea, Sweden
[4] Univ Rijeka, Dept Biotechnol, HR-51000 Rijeka, Croatia
[5] Vilnius Univ, Life Sci Ctr, Inst Biotechnol, LT-10257 Vilnius, Lithuania
来源
ACS CHEMICAL NEUROSCIENCE | 2021年 / 12卷 / 11期
基金
瑞典研究理事会; 英国医学研究理事会;
关键词
amyloid; cytotoxicity; neurodegeneration; oleuropein aglycone; plant polyphenols; S100A9; CELLULAR PRION PROTEIN; COGNITIVE IMPAIRMENT; MEMBRANE DISRUPTION; IN-VITRO; EXPRESSION; MECHANISM; OLIGOMERS; NEUROINFLAMMATION; INFLAMMATION; BIOMARKER;
D O I
10.1021/acschemneuro.0c00828
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
Polyphenolic compounds in the Mediterranean diet have received increasing attention due to their protective properties in amyloid neurodegenerative and many other diseases. Here, we have demonstrated for the first time that polyphenol oleuropein aglycone (OleA), which is the most abundant compound in olive oil, has multiple potencies for the inhibition of amyloid self-assembly of pro-inflammatory protein S100A9 and the mitigation of the damaging effect of its amyloids on neuroblastoma SH-SY5Y cells. OleA directly interacts with both native and fibrillar S100A9 as shown by intrinsic fluorescence and molecular dynamic simulation. OleA prevents S100A9 amyloid oligomerization as shown using amyloid oligomer-specific antibodies and cross-beta-sheet formation detected by circular dichroism. It decreases the length of amyloid fibrils measured by atomic force microscopy (AFM) as well as reduces the effective rate of amyloid growth and the overall amyloid load as derived from the kinetic analysis of amyloid formation. OleA disintegrates already preformed fibrils of S100A9, converting them into nonfibrillar and nontoxic aggregates as revealed by amyloid thioflavin-T dye binding, AFM, and cytotoxicity assays. At the cellular level, OleA targets S100A9 amyloids already at the membranes as shown by immunofluorescence and fluorescence resonance energy transfer, significantly reducing the amyloid accumulation in GM1 ganglioside containing membrane rafts. OleA increases overall cell viability when neuroblastoma cells are subjected to the amyloid load and alleviates amyloid-induced intracellular rise of reactive oxidative species and free Ca2+. Since S100A9 is both a pro-inflammatory and amyloidogenic protein, OleA may effectively mitigate the pathological consequences of the S100A9-dependent amyloid-neuroinflammatory cascade as well as provide protection from neurodegeneration, if used within the Mediterranean diet as a potential preventive measure.
引用
收藏
页码:1905 / 1918
页数:14
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