Attenuation of β-amyloid induced toxicity by sialic acid-conjugated dendrimeric polymers

• Published in: Biochimica et biophysica acta Vol. 1760; no. 12; pp. 1802 - 1809
• Main Authors: Patel, Dhara, Henry, James, Good, Theresa
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 01.12.2006
• Subjects: Alzheimer's disease; Amyloid; Amyloid beta-Peptides - toxicity; Cell Line, Tumor; Dendrimer; Dendrimers - chemistry; Flow Cytometry; Humans; N-Acetylneuraminic Acid - chemistry; Sialic acid; Toxicity; Dendrimer; Sialic acid; Amyloid; Toxicity; Alzheimer's disease
• ISSN: 0304-4165; 0006-3002; 1872-8006
• DOI: 10.1016/j.bbagen.2006.08.008

β-amyloid (Aβ) is the primary protein component of senile plaques in Alzheimer's disease and is believed to be associated with neurotoxicity in the disease. We and others have shown that Aβ binds with relatively high affinity to clustered sialic acid residues on cell surfaces and that removal of cell surface sialic acids attenuate Aβ toxicity. In the current work, we have prepared sialic acid conjugated dendrimeric polymers and assessed the ability of these sialic acid conjugated dendrimers to prevent Aβ toxicity. Flow cytometry was used to analyze viability of SH-SY5Y neuroblastoma cells and the effects of soluble and clustered sialic acid mimics on Aβ cell toxicity. Soluble sialic acid attenuation of Aβ induced toxicity was effective only at high sialic acid concentrations and low Aβ concentration. The sialic acid conjugated dendrimeric polymers were able to attenuate Aβ toxicity at micromolar concentrations, or approximately three orders of magnitude lower concentrations than the soluble sialic acid. The toxicity prevention properties of the sialic acid modified dendrimers were a function of dendrimer size. This work may lead to the development of new classes of therapeutics for the prevention of Aβ toxicity.