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Eryptosis Indices as a Novel Predictive Parameter for Biocompatibility of Fe(3)O(4) Magnetic Nanoparticles on Erythrocytes

Fe(3)O(4) magnetic nanoparticles (Fe(3)O(4)-MNPs) have been widely used in clinical diagnosis. Hemocompatibility of the nanoparticles is usually evaluated by hemolysis. However, hemolysis assessment does not measure the dysfunctional erythrocytes with pathological changes on the unbroken cellular me...

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Autores principales: Ran, Qian, Xiang, Yang, Liu, Yao, Xiang, Lixin, Li, Fengjie, Deng, Xiaojun, Xiao, Yanni, Chen, Li, Chen, Lili, Li, Zhongjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4633654/
https://www.ncbi.nlm.nih.gov/pubmed/26537855
http://dx.doi.org/10.1038/srep16209
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author Ran, Qian
Xiang, Yang
Liu, Yao
Xiang, Lixin
Li, Fengjie
Deng, Xiaojun
Xiao, Yanni
Chen, Li
Chen, Lili
Li, Zhongjun
author_facet Ran, Qian
Xiang, Yang
Liu, Yao
Xiang, Lixin
Li, Fengjie
Deng, Xiaojun
Xiao, Yanni
Chen, Li
Chen, Lili
Li, Zhongjun
author_sort Ran, Qian
collection PubMed
description Fe(3)O(4) magnetic nanoparticles (Fe(3)O(4)-MNPs) have been widely used in clinical diagnosis. Hemocompatibility of the nanoparticles is usually evaluated by hemolysis. However, hemolysis assessment does not measure the dysfunctional erythrocytes with pathological changes on the unbroken cellular membrane. The aim of this study is to evaluate the use of suicidal death of erythrocytes (i.e. eryptosis indices) as a novel predictive and prognostic parameter, and to determine the impact of Fe(3)O(4)-MNPs on cellular membrane structure and the rheology properties of blood in circulation. Our results showed that phosphatidylserine externalization assessment was significantly more sensitive than classical hemolysis testing in evaluating hemocompatibility. Although no remarkable changes of histopathology, hematology and serum biochemistry indices were observed in vivo, Fe(3)O(4)-MNPs significantly affected hemorheology indices including erythrocyte deformation index, erythrocyte rigidity index, red blood cell aggregation index, and erythrocyte electrophoresis time, which are related to the mechanical properties of the erythrocytes. Oxidative stress induced calcium influx played a critical role in the eryptotic activity of Fe(3)O(4)-MNPs. This study demonstrated that Fe(3)O(4)-MNPs cause eryptosis and changes in flow properties of blood, suggesting that phosphatidylserine externalization can serve as a predictive parameter for hemocompatibility assay.
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spelling pubmed-46336542015-11-05 Eryptosis Indices as a Novel Predictive Parameter for Biocompatibility of Fe(3)O(4) Magnetic Nanoparticles on Erythrocytes Ran, Qian Xiang, Yang Liu, Yao Xiang, Lixin Li, Fengjie Deng, Xiaojun Xiao, Yanni Chen, Li Chen, Lili Li, Zhongjun Sci Rep Article Fe(3)O(4) magnetic nanoparticles (Fe(3)O(4)-MNPs) have been widely used in clinical diagnosis. Hemocompatibility of the nanoparticles is usually evaluated by hemolysis. However, hemolysis assessment does not measure the dysfunctional erythrocytes with pathological changes on the unbroken cellular membrane. The aim of this study is to evaluate the use of suicidal death of erythrocytes (i.e. eryptosis indices) as a novel predictive and prognostic parameter, and to determine the impact of Fe(3)O(4)-MNPs on cellular membrane structure and the rheology properties of blood in circulation. Our results showed that phosphatidylserine externalization assessment was significantly more sensitive than classical hemolysis testing in evaluating hemocompatibility. Although no remarkable changes of histopathology, hematology and serum biochemistry indices were observed in vivo, Fe(3)O(4)-MNPs significantly affected hemorheology indices including erythrocyte deformation index, erythrocyte rigidity index, red blood cell aggregation index, and erythrocyte electrophoresis time, which are related to the mechanical properties of the erythrocytes. Oxidative stress induced calcium influx played a critical role in the eryptotic activity of Fe(3)O(4)-MNPs. This study demonstrated that Fe(3)O(4)-MNPs cause eryptosis and changes in flow properties of blood, suggesting that phosphatidylserine externalization can serve as a predictive parameter for hemocompatibility assay. Nature Publishing Group 2015-11-05 /pmc/articles/PMC4633654/ /pubmed/26537855 http://dx.doi.org/10.1038/srep16209 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Ran, Qian
Xiang, Yang
Liu, Yao
Xiang, Lixin
Li, Fengjie
Deng, Xiaojun
Xiao, Yanni
Chen, Li
Chen, Lili
Li, Zhongjun
Eryptosis Indices as a Novel Predictive Parameter for Biocompatibility of Fe(3)O(4) Magnetic Nanoparticles on Erythrocytes
title Eryptosis Indices as a Novel Predictive Parameter for Biocompatibility of Fe(3)O(4) Magnetic Nanoparticles on Erythrocytes
title_full Eryptosis Indices as a Novel Predictive Parameter for Biocompatibility of Fe(3)O(4) Magnetic Nanoparticles on Erythrocytes
title_fullStr Eryptosis Indices as a Novel Predictive Parameter for Biocompatibility of Fe(3)O(4) Magnetic Nanoparticles on Erythrocytes
title_full_unstemmed Eryptosis Indices as a Novel Predictive Parameter for Biocompatibility of Fe(3)O(4) Magnetic Nanoparticles on Erythrocytes
title_short Eryptosis Indices as a Novel Predictive Parameter for Biocompatibility of Fe(3)O(4) Magnetic Nanoparticles on Erythrocytes
title_sort eryptosis indices as a novel predictive parameter for biocompatibility of fe(3)o(4) magnetic nanoparticles on erythrocytes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4633654/
https://www.ncbi.nlm.nih.gov/pubmed/26537855
http://dx.doi.org/10.1038/srep16209
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