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
  • [21] Methionine oxidation:: Implications for the mechanism of toxicity of the β-amyloid peptide from Alzheimer's disease
    Ciccotosto, GD
    Barnham, KJ
    Cherny, RA
    Masters, CL
    Bush, AI
    Curtain, CC
    Cappai, R
    Tew, D
    LETTERS IN PEPTIDE SCIENCE, 2003, 10 (5-6): : 413 - 417
  • [22] Methionine oxidation: Implications for the mechanism of toxicity of the β-amyloid peptide from Alzheimer's disease
    Giuseppe D. Ciccotosto
    Kevin J. Barnham
    Robert A. Cherny
    Colin L. Masters
    Ashley I. Bush
    Cyril C. Curtain
    Roberto Cappai
    Deborah Tew
    Letters in Peptide Science, 2003, 10 : 413 - 417
  • [23] Extra-Virgin Olive Oil and Oleocanthal Reduce Amyloid-β Load in Alzheimer's Disease Mouse Model
    Batarseh, Yazan
    Qosa, Hisham
    Elsayed, Khalid
    Keller, Jeffrey
    Kaddoumi, Amal
    2016 32ND SOUTHERN BIOMEDICAL ENGINEERING CONFERENCE (SBEC), 2016, : 92 - 92
  • [24] New class of inhibitors of amyloid-β fibril formation -: Implications for the mechanism of pathogenesis in Alzheimer's disease
    Lashuel, HA
    Hartley, DM
    Balakhaneh, D
    Aggarwal, A
    Teichberg, S
    Callaway, DJE
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (45) : 42881 - 42890
  • [25] Posttranslational Nitro-Glycative Modifications of Albumin in Alzheimer's Disease: Implications in Cytotoxicity and Amyloid-β Peptide Aggregation
    Ramos-Fernandez, Eva
    Tajes, Marta
    Palomer, Ernest
    Ill-Raga, Gerard
    Bosch-Morato, Monica
    Guivernau, Biuse
    Roman-Degano, Irene
    Eraso-Pichot, Abel
    Alcolea, Daniel
    Fortea, Juan
    Nunez, Laura
    Paez, Antonio
    Alameda, Francesc
    Fernandez-Busquets, Xavier
    Lleo, Alberto
    Elosua, Roberto
    Boada, Merce
    Valverde, Miguel A.
    Munoz, Francisco J.
    JOURNAL OF ALZHEIMERS DISEASE, 2014, 40 (03) : 643 - 657
  • [26] S100A9-Driven Amyloid-Neuroinflammatory Cascade in Traumatic Brain Injury as a Precursor State for Alzheimer's Disease
    Wang, Chao
    Iashchishyn, Igor A.
    Pansieri, Jonathan
    Nystrom, Sofie
    Klementieva, Oxana
    Kara, John
    Horvath, Istvan
    Moskalenko, Roman
    Rofougaran, Reza
    Gouras, Gunnar
    Kovacs, Gabor G.
    Shankar, S. K.
    Morozova-Roche, Ludmilla A.
    SCIENTIFIC REPORTS, 2018, 8
  • [27] S100A9-Driven Amyloid-Neuroinflammatory Cascade in Traumatic Brain Injury as a Precursor State for Alzheimer’s Disease
    Chao Wang
    Igor A. Iashchishyn
    Jonathan Pansieri
    Sofie Nyström
    Oxana Klementieva
    John Kara
    Istvan Horvath
    Roman Moskalenko
    Reza Rofougaran
    Gunnar Gouras
    Gabor G. Kovacs
    S. K. Shankar
    Ludmilla A. Morozova-Roche
    Scientific Reports, 8
  • [28] Release of β-amyloid from high-density platelets -: Implications for Alzheimer's disease pathology
    Casoli, Tiziana
    Di Stefano, Giuseppina
    Giorgetti, Belinda
    Grossi, Yessica
    Balietti, Marta
    Fattoretti, Patrizia
    Bertoni-Freddari, Carlo
    SIGNAL TRANSDUCTION PATHWAYS, PT D: INFLAMMATORY SIGNALING PATHWAYS AND NEUROPATHOLOGY, 2007, 1096 : 170 - 178
  • [29] From Mitochondrial Dysfunction to Amyloid Beta Formation: Novel Insights into the Pathogenesis of Alzheimer's Disease
    Leuner, Kristina
    Mueller, Walter E.
    Reichert, Andreas S.
    MOLECULAR NEUROBIOLOGY, 2012, 46 (01) : 186 - 193
  • [30] From Mitochondrial Dysfunction to Amyloid Beta Formation: Novel Insights into the Pathogenesis of Alzheimer’s Disease
    Kristina Leuner
    Walter E. Müller
    Andreas S. Reichert
    Molecular Neurobiology, 2012, 46 : 186 - 193