Abstract
Three different amyloid targeting ligands, previously shown to exhibit amyloid specific properties, have been used to develop amyloid -targeted nanoliposomes (AT-NLs). For this a MAb against Aβ-peptides (Aβ-MAb) (immobilized on NLs at 0.015 and 0.05 mol %), and two different curcumin-lipid derivatives were attached to the surface of preformed NLs or incorporated in NL membranes during their formation. Following physicochemical characterization, these AT-NLs were studied for their ability to inhibit or delay amyloid peptide aggregation –using the thioflavin-T assay, and for their potential to reverse amyloid-induced (and Zn, or, amyloid + Zn) cytotoxicity, on wild type (N2aWT) and transformed (N2aAPP) neuroblastoma cells, applying the MTT assay. Experimental results reveal that all formulations were found to strongly delay amyloid peptide aggregation (with no significant differences between the different AT-NL types). However, although Aβ-MAb-NLs significantly reversed amyloid-induced cytotoxicity in all cases, both curcumin-NL types did not reverse Zn-induced, nor Zn+Aβ-induced cytotoxicity in N2aWT cells, suggesting lower activity against synthetic-Aβ peptides (compared to endogenous Aβ peptides); perhaps due to different affinity towards different (aggregation stages of) peptide species (monomers, oligomers, fibrils, etc). Taken into account that the aggregation stage of amyloid species is an important determinant of their toxicity, the importance of the affinity of each AT-NL type towards specific species, is highlighted.
Keywords: Alzheimer’s disease, Amyloid, Aggregation, Curcumin, Liposomes, Monoclonal Antibody, Nanoparticle, Targeting.
Current Topics in Medicinal Chemistry
Title:Comparison of Various Types of Ligand Decorated Nanoliposomes for their Ability to Inhibit Amyloid Aggregation and to Reverse Amyloid Cytotoxicity
Volume: 15 Issue: 22
Author(s): Eleni Markoutsa, Spyridon Mourtas, Erika Bereczki, Cristiano Zona, Barbara La Ferla, Fransesco Nicotra, Orfeu Flores, Jin-Jing Pei and Sophia G. Antimisiaris
Affiliation:
Keywords: Alzheimer’s disease, Amyloid, Aggregation, Curcumin, Liposomes, Monoclonal Antibody, Nanoparticle, Targeting.
Abstract: Three different amyloid targeting ligands, previously shown to exhibit amyloid specific properties, have been used to develop amyloid -targeted nanoliposomes (AT-NLs). For this a MAb against Aβ-peptides (Aβ-MAb) (immobilized on NLs at 0.015 and 0.05 mol %), and two different curcumin-lipid derivatives were attached to the surface of preformed NLs or incorporated in NL membranes during their formation. Following physicochemical characterization, these AT-NLs were studied for their ability to inhibit or delay amyloid peptide aggregation –using the thioflavin-T assay, and for their potential to reverse amyloid-induced (and Zn, or, amyloid + Zn) cytotoxicity, on wild type (N2aWT) and transformed (N2aAPP) neuroblastoma cells, applying the MTT assay. Experimental results reveal that all formulations were found to strongly delay amyloid peptide aggregation (with no significant differences between the different AT-NL types). However, although Aβ-MAb-NLs significantly reversed amyloid-induced cytotoxicity in all cases, both curcumin-NL types did not reverse Zn-induced, nor Zn+Aβ-induced cytotoxicity in N2aWT cells, suggesting lower activity against synthetic-Aβ peptides (compared to endogenous Aβ peptides); perhaps due to different affinity towards different (aggregation stages of) peptide species (monomers, oligomers, fibrils, etc). Taken into account that the aggregation stage of amyloid species is an important determinant of their toxicity, the importance of the affinity of each AT-NL type towards specific species, is highlighted.
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Markoutsa Eleni, Mourtas Spyridon, Bereczki Erika, Zona Cristiano, Ferla La Barbara, Nicotra Fransesco, Flores Orfeu, Pei Jin-Jing and Antimisiaris G. Sophia, Comparison of Various Types of Ligand Decorated Nanoliposomes for their Ability to Inhibit Amyloid Aggregation and to Reverse Amyloid Cytotoxicity, Current Topics in Medicinal Chemistry 2015; 15 (22) . https://dx.doi.org/10.2174/1568026615666150605115902
DOI https://dx.doi.org/10.2174/1568026615666150605115902 |
Print ISSN 1568-0266 |
Publisher Name Bentham Science Publisher |
Online ISSN 1873-4294 |
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