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
英国医学研究理事会; 瑞典研究理事会;
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
相关论文
共 50 条
  • [31] Alzheimer's Disease May Benefit from Olive Oil Polyphenols: A Systematic Review on Preclinical Evidence Supporting the Effect of Oleocanthal on Amyloid-β Load
    Zupo, Roberta
    Castellana, Fabio
    Panza, Francesco
    Solfrizzi, Vincenzo
    Lozupone, Madia
    Tardugno, Roberta
    Cicero, Nicola
    Corbo, Filomena
    Crupi, Pasquale
    Sardone, Rodolfo
    Clodoveo, Maria Lisa
    CURRENT NEUROPHARMACOLOGY, 2024,
  • [32] Alzheimer's Disease: Insights into Amyloid Fibril Formation from Lattice Monte Carlo Simulations
    Thanh-Thuy Tran
    Nguyen, Phuong H.
    Derreumaux, Philippe
    BIOPHYSICAL JOURNAL, 2016, 110 (03) : 219A - 219A
  • [33] Impact of Four Common Hydrogels on Amyloid-β (Aβ) Aggregation and Cytotoxicity: Implications for 3D Models of Alzheimer's Disease
    Simpson, Laura W.
    Szeto, Gregory L.
    Boukari, Hacene
    Good, Theresa A.
    Leach, Jennie B.
    ACS OMEGA, 2020, 5 (32): : 20250 - 20260
  • [34] Mechanism of amyloid beta peptides and alfa synuclein cytotoxicity. The role of PARPs and sirtuins. Implications in Alzheimer's disease
    Wencel, P. L.
    Motyl, J.
    Strosznajder, J. B.
    Strosznajder, R. P.
    EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2016, 26 : S653 - S653
  • [35] CYSTATIN C BINDS AMYLOID β AND INHIBITS ITS OLIGOMERIZATION, FIBRIL FORMATION, AND DEPOSITION IN ALZHEIMER'S DISEASE MOUSE MODELS
    Levy, Efrat
    NEUROPEPTIDES, 2009, 43 (02) : 149 - 150
  • [36] Ube3a deficiency inhibits amyloid plaque formation in APPswe/PS1δE9 mouse model of Alzheimer's disease
    Singh, Brijesh Kumar
    Vatsa, Naman
    Kumar, Vipendra
    Shekhar, Shashi
    Sharma, Ankit
    Jana, Nihar Ranjan
    HUMAN MOLECULAR GENETICS, 2017, 26 (20) : 4042 - 4054
  • [37] Clinicopathologic and 11C-Pittsburgh compound B implications of Thal amyloid phase across the Alzheimer's disease spectrum
    Murray, Melissa E.
    Lowe, Val J.
    Graff-Radford, Neill R.
    Liesinger, Amanda M.
    Cannon, Ashley
    Przybelski, Scott A.
    Rawal, Bhupendra
    Parisi, Joseph E.
    Petersen, Ronald C.
    Kantarci, Kejal
    Ross, Owen A.
    Duara, Ranjan
    Knopman, David S.
    Jack, Clifford R., Jr.
    Dickson, Dennis W.
    BRAIN, 2015, 138 : 1370 - 1381
  • [38] S100A9, an inflammation-associated calcium-binding protein, is a binding partner for various redox-regulating proteins in familial Alzheimer's disease
    Rahimi, F
    Goyette, J
    Raftery, M
    Shepherd, C
    Halliday, G
    Geczy, C
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 2005, 238 : S298 - S298
  • [39] The misfolded pro-inflammatory protein S100A9 disrupts memory via neurochemical remodelling instigating an Alzheimer's disease-like cognitive deficit
    Gruden, Marina A.
    Davydova, Tatiana V.
    Wang, Chao
    Narkevich, Victor B.
    Fomina, Valentina G.
    Kudrin, Vladimir S.
    Morozova-Roche, Ludmilla A.
    Sewell, Robert D. E.
    BEHAVIOURAL BRAIN RESEARCH, 2016, 306 : 106 - 116
  • [40] Finke-Watzky Two-Step Nucleation-Autocatalysis Model of S100A9 Amyloid Formation: Protein Misfolding as "Nucleation" Event
    Iashchishyn, Igor A.
    Sulskis, Darius
    Mai Nguyen Ngoc
    Smirnovas, Vytautas
    Morozova-Roche, Ludmilla A.
    ACS CHEMICAL NEUROSCIENCE, 2017, 8 (10): : 2152 - 2158