Issue 80, 2016

Low generation anionic dendrimers modulate islet amyloid polypeptide self-assembly and inhibit pancreatic β-cell toxicity

Abstract

The deposition of the islet amyloid polypeptide (IAPP) as insoluble amyloid fibrils in the pancreatic islets is associated with type II diabetes. Recent studies have revealed that pre-fibrillar proteospecies and/or the amyloidogenic process mediate β-cell degeneration whereas amyloid fibrils are poorly cytotoxic. Thus, therapeutic strategies that aim at preventing β-cell death associated with amyloid deposition should either sequester prefibrillar species and/or modulate the initial steps of fibrillization. In this view, low generation flexible dendritic scaffolds harboring 4 to 16 hydroxyl, amine, carboxylate or sulfate functional groups were designed and evaluated for their effects on IAPP self-assembly and cytotoxicity. Whereas neutral polyhydroxylated and polycationic dendrimers did not affect the kinetics of amyloid assembly, carboxylated dendrimers accelerated IAPP fibrillization proportionally to surface group density. Interestingly, as revealed by thioflavin T fluorescence, circular dichroism spectroscopy and atomic force microscopy, the G0 sulfated dendrimer inhibited amyloid formation by maintaining the peptide in a random coil conformation. In contrast, G1 sulfated dendrimers potentiated IAPP self-assembly into long amyloid fibrils by a scaffold-based mechanism. Anionic dendrimers attenuated IAPP-induced toxicity on pancreatic β-cells. Our results indicate that sulfated dendrimers can alter the fibrillization pathway of IAPP and inhibit its proteotoxicity, either by accelerating amyloid formation or by trapping the peptide in a non-aggregating and non-toxic state. This study offers novel mechanistic insights for the design of a nanomolecular scaffold to manipulate the self-assembly of natively disordered amyloidogenic peptides.

Graphical abstract: Low generation anionic dendrimers modulate islet amyloid polypeptide self-assembly and inhibit pancreatic β-cell toxicity

Supplementary files

Article information

Article type
Paper
Submitted
13 Jūn. 2016
Accepted
24 Jūl. 2016
First published
05 Aug. 2016

RSC Adv., 2016,6, 76360-76369

Low generation anionic dendrimers modulate islet amyloid polypeptide self-assembly and inhibit pancreatic β-cell toxicity

P. T. Nguyen, R. Sharma, R. Rej, C. A. De Carufel, R. Roy and S. Bourgault, RSC Adv., 2016, 6, 76360 DOI: 10.1039/C6RA15373A

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements