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Substantial fibrin amyloidogenesis in type 2 diabetes assessed using amyloid-selective fluorescent stains
BACKGROUND: We have previously shown that many chronic, inflammatory diseases are accompanied, and possibly partly caused or exacerbated, by various coagulopathies, manifested as anomalous clots in the form of ‘dense matted deposits’. More recently, we have shown that these clots can be amyloid in n...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5668975/ https://www.ncbi.nlm.nih.gov/pubmed/29096623 http://dx.doi.org/10.1186/s12933-017-0624-5 |
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author | Pretorius, Etheresia Page, Martin J. Engelbrecht, Lize Ellis, Graham C. Kell, Douglas B. |
author_facet | Pretorius, Etheresia Page, Martin J. Engelbrecht, Lize Ellis, Graham C. Kell, Douglas B. |
author_sort | Pretorius, Etheresia |
collection | PubMed |
description | BACKGROUND: We have previously shown that many chronic, inflammatory diseases are accompanied, and possibly partly caused or exacerbated, by various coagulopathies, manifested as anomalous clots in the form of ‘dense matted deposits’. More recently, we have shown that these clots can be amyloid in nature, and that the plasma of healthy controls can be induced to form such clots by the addition of tiny amounts of bacterial lipopolysaccharide or lipoteichoic acid. Type 2 diabetes (T2D) is also accompanied by raised levels of LPS. METHODS: We use superresolution and confocal microscopies to investigate the amyloid nature of clots from healthy and T2D individuals. RESULTS: We show here, with the established stain thioflavin T and the novel stains Amytracker™ 480 and 680, that the clotting of plasma from type 2 diabetics is also amyloid in nature, and that this may be prevented by the addition of suitable concentrations of LPS-binding protein. CONCLUSION: This implies strongly that there is indeed a microbial component to the development of type 2 diabetes, and suggests that LBP might be used as treatment for it and its sequelae. |
format | Online Article Text |
id | pubmed-5668975 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-56689752017-11-08 Substantial fibrin amyloidogenesis in type 2 diabetes assessed using amyloid-selective fluorescent stains Pretorius, Etheresia Page, Martin J. Engelbrecht, Lize Ellis, Graham C. Kell, Douglas B. Cardiovasc Diabetol Original Investigation BACKGROUND: We have previously shown that many chronic, inflammatory diseases are accompanied, and possibly partly caused or exacerbated, by various coagulopathies, manifested as anomalous clots in the form of ‘dense matted deposits’. More recently, we have shown that these clots can be amyloid in nature, and that the plasma of healthy controls can be induced to form such clots by the addition of tiny amounts of bacterial lipopolysaccharide or lipoteichoic acid. Type 2 diabetes (T2D) is also accompanied by raised levels of LPS. METHODS: We use superresolution and confocal microscopies to investigate the amyloid nature of clots from healthy and T2D individuals. RESULTS: We show here, with the established stain thioflavin T and the novel stains Amytracker™ 480 and 680, that the clotting of plasma from type 2 diabetics is also amyloid in nature, and that this may be prevented by the addition of suitable concentrations of LPS-binding protein. CONCLUSION: This implies strongly that there is indeed a microbial component to the development of type 2 diabetes, and suggests that LBP might be used as treatment for it and its sequelae. BioMed Central 2017-11-02 /pmc/articles/PMC5668975/ /pubmed/29096623 http://dx.doi.org/10.1186/s12933-017-0624-5 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Original Investigation Pretorius, Etheresia Page, Martin J. Engelbrecht, Lize Ellis, Graham C. Kell, Douglas B. Substantial fibrin amyloidogenesis in type 2 diabetes assessed using amyloid-selective fluorescent stains |
title | Substantial fibrin amyloidogenesis in type 2 diabetes assessed using amyloid-selective fluorescent stains |
title_full | Substantial fibrin amyloidogenesis in type 2 diabetes assessed using amyloid-selective fluorescent stains |
title_fullStr | Substantial fibrin amyloidogenesis in type 2 diabetes assessed using amyloid-selective fluorescent stains |
title_full_unstemmed | Substantial fibrin amyloidogenesis in type 2 diabetes assessed using amyloid-selective fluorescent stains |
title_short | Substantial fibrin amyloidogenesis in type 2 diabetes assessed using amyloid-selective fluorescent stains |
title_sort | substantial fibrin amyloidogenesis in type 2 diabetes assessed using amyloid-selective fluorescent stains |
topic | Original Investigation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5668975/ https://www.ncbi.nlm.nih.gov/pubmed/29096623 http://dx.doi.org/10.1186/s12933-017-0624-5 |
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