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Cryogenic Transmission Electron Microscopy Nanostructural Study of Shed Microparticles
Microparticles (MPs) are sub-micron membrane vesicles (100–1000 nm) shed from normal and pathologic cells due to stimulation or apoptosis. MPs can be found in the peripheral blood circulation of healthy individuals, whereas elevated concentrations are found in pregnancy and in a variety of diseases....
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3873325/ https://www.ncbi.nlm.nih.gov/pubmed/24386253 http://dx.doi.org/10.1371/journal.pone.0083680 |
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author | Issman, Liron Brenner, Benjamin Talmon, Yeshayahu Aharon, Anat |
author_facet | Issman, Liron Brenner, Benjamin Talmon, Yeshayahu Aharon, Anat |
author_sort | Issman, Liron |
collection | PubMed |
description | Microparticles (MPs) are sub-micron membrane vesicles (100–1000 nm) shed from normal and pathologic cells due to stimulation or apoptosis. MPs can be found in the peripheral blood circulation of healthy individuals, whereas elevated concentrations are found in pregnancy and in a variety of diseases. Also, MPs participate in physiological processes, e.g., coagulation, inflammation, and angiogenesis. Since their clinical properties are important, we have developed a new methodology based on nano-imaging that provides significant new data on MPs nanostructure, their composition and function. We are among the first to characterize by direct-imaging cryogenic transmitting electron microscopy (cryo-TEM) the near-to-native nanostructure of MP systems isolated from different cell types and stimulation procedures. We found that there are no major differences between the MP systems we have studied, as most particles were spherical, with diameters from 200 to 400 nm. However, each MP population is very heterogeneous, showing diverse morphologies. We investigated by cryo-TEM the effects of standard techniques used to isolate and store MPs, and found that either high-g centrifugation of MPs for isolation purposes, or slow freezing to –80°C for storage introduce morphological artifacts, which can influence MP nanostructure, and thus affect the efficiency of these particles as future diagnostic tools. |
format | Online Article Text |
id | pubmed-3873325 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-38733252014-01-02 Cryogenic Transmission Electron Microscopy Nanostructural Study of Shed Microparticles Issman, Liron Brenner, Benjamin Talmon, Yeshayahu Aharon, Anat PLoS One Research Article Microparticles (MPs) are sub-micron membrane vesicles (100–1000 nm) shed from normal and pathologic cells due to stimulation or apoptosis. MPs can be found in the peripheral blood circulation of healthy individuals, whereas elevated concentrations are found in pregnancy and in a variety of diseases. Also, MPs participate in physiological processes, e.g., coagulation, inflammation, and angiogenesis. Since their clinical properties are important, we have developed a new methodology based on nano-imaging that provides significant new data on MPs nanostructure, their composition and function. We are among the first to characterize by direct-imaging cryogenic transmitting electron microscopy (cryo-TEM) the near-to-native nanostructure of MP systems isolated from different cell types and stimulation procedures. We found that there are no major differences between the MP systems we have studied, as most particles were spherical, with diameters from 200 to 400 nm. However, each MP population is very heterogeneous, showing diverse morphologies. We investigated by cryo-TEM the effects of standard techniques used to isolate and store MPs, and found that either high-g centrifugation of MPs for isolation purposes, or slow freezing to –80°C for storage introduce morphological artifacts, which can influence MP nanostructure, and thus affect the efficiency of these particles as future diagnostic tools. Public Library of Science 2013-12-26 /pmc/articles/PMC3873325/ /pubmed/24386253 http://dx.doi.org/10.1371/journal.pone.0083680 Text en © 2013 Issman et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Issman, Liron Brenner, Benjamin Talmon, Yeshayahu Aharon, Anat Cryogenic Transmission Electron Microscopy Nanostructural Study of Shed Microparticles |
title | Cryogenic Transmission Electron Microscopy Nanostructural Study of Shed Microparticles |
title_full | Cryogenic Transmission Electron Microscopy Nanostructural Study of Shed Microparticles |
title_fullStr | Cryogenic Transmission Electron Microscopy Nanostructural Study of Shed Microparticles |
title_full_unstemmed | Cryogenic Transmission Electron Microscopy Nanostructural Study of Shed Microparticles |
title_short | Cryogenic Transmission Electron Microscopy Nanostructural Study of Shed Microparticles |
title_sort | cryogenic transmission electron microscopy nanostructural study of shed microparticles |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3873325/ https://www.ncbi.nlm.nih.gov/pubmed/24386253 http://dx.doi.org/10.1371/journal.pone.0083680 |
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