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Evaluation of techniques for performing cellular isolation and preservation during microgravity conditions
Genomic and epigenomic studies require the precise transfer of microliter volumes among different types of tubes in order to purify DNA, RNA, or protein from biological samples and subsequently perform analyses of DNA methylation, RNA expression, and chromatin modifications on a genome-wide scale. E...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5515526/ https://www.ncbi.nlm.nih.gov/pubmed/28725735 http://dx.doi.org/10.1038/npjmgrav.2016.25 |
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author | Rizzardi, Lindsay F Kunz, Hawley Rubins, Kathleen Chouker, Alexander Quiriarte, Heather Sams, Clarence Crucian, Brian E Feinberg, Andrew P |
author_facet | Rizzardi, Lindsay F Kunz, Hawley Rubins, Kathleen Chouker, Alexander Quiriarte, Heather Sams, Clarence Crucian, Brian E Feinberg, Andrew P |
author_sort | Rizzardi, Lindsay F |
collection | PubMed |
description | Genomic and epigenomic studies require the precise transfer of microliter volumes among different types of tubes in order to purify DNA, RNA, or protein from biological samples and subsequently perform analyses of DNA methylation, RNA expression, and chromatin modifications on a genome-wide scale. Epigenomic and transcriptional analyses of human blood cells, for example, require separation of purified cell types to avoid confounding contributions of altered cellular proportions, and long-term preservation of these cells requires their isolation and transfer into appropriate freezing media. There are currently no protocols for these cellular isolation procedures on the International Space Station (ISS). Currently human blood samples are either frozen as mixed cell populations (within the CPT collection tubes) with poor yield of viable cells required for cell-type isolations, or returned under ambient conditions, which requires timing with Soyuz missions. Here we evaluate the feasibility of translating terrestrial cell purification techniques to the ISS. Our evaluations were performed in microgravity conditions during parabolic atmospheric flight. The pipetting of open liquids in microgravity was evaluated using analog-blood fluids and several types of pipette hardware. The best-performing pipettors were used to evaluate the pipetting steps required for peripheral blood mononuclear cell (PBMC) isolation following terrestrial density-gradient centrifugation. Evaluation of actual blood products was performed for both the overlay of diluted blood, and the transfer of isolated PBMCs. We also validated magnetic purification of cells. We found that positive-displacement pipettors avoided air bubbles, and the tips allowed the strong surface tension of water, glycerol, and blood to maintain a patent meniscus and withstand robust pipetting in microgravity. These procedures will greatly increase the breadth of research that can be performed on board the ISS, and allow improvised experimentation by astronauts on extraterrestrial missions. |
format | Online Article Text |
id | pubmed-5515526 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-55155262017-07-19 Evaluation of techniques for performing cellular isolation and preservation during microgravity conditions Rizzardi, Lindsay F Kunz, Hawley Rubins, Kathleen Chouker, Alexander Quiriarte, Heather Sams, Clarence Crucian, Brian E Feinberg, Andrew P NPJ Microgravity Article Genomic and epigenomic studies require the precise transfer of microliter volumes among different types of tubes in order to purify DNA, RNA, or protein from biological samples and subsequently perform analyses of DNA methylation, RNA expression, and chromatin modifications on a genome-wide scale. Epigenomic and transcriptional analyses of human blood cells, for example, require separation of purified cell types to avoid confounding contributions of altered cellular proportions, and long-term preservation of these cells requires their isolation and transfer into appropriate freezing media. There are currently no protocols for these cellular isolation procedures on the International Space Station (ISS). Currently human blood samples are either frozen as mixed cell populations (within the CPT collection tubes) with poor yield of viable cells required for cell-type isolations, or returned under ambient conditions, which requires timing with Soyuz missions. Here we evaluate the feasibility of translating terrestrial cell purification techniques to the ISS. Our evaluations were performed in microgravity conditions during parabolic atmospheric flight. The pipetting of open liquids in microgravity was evaluated using analog-blood fluids and several types of pipette hardware. The best-performing pipettors were used to evaluate the pipetting steps required for peripheral blood mononuclear cell (PBMC) isolation following terrestrial density-gradient centrifugation. Evaluation of actual blood products was performed for both the overlay of diluted blood, and the transfer of isolated PBMCs. We also validated magnetic purification of cells. We found that positive-displacement pipettors avoided air bubbles, and the tips allowed the strong surface tension of water, glycerol, and blood to maintain a patent meniscus and withstand robust pipetting in microgravity. These procedures will greatly increase the breadth of research that can be performed on board the ISS, and allow improvised experimentation by astronauts on extraterrestrial missions. Nature Publishing Group 2016-07-14 /pmc/articles/PMC5515526/ /pubmed/28725735 http://dx.doi.org/10.1038/npjmgrav.2016.25 Text en Copyright © 2016 The Author(s) 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 Rizzardi, Lindsay F Kunz, Hawley Rubins, Kathleen Chouker, Alexander Quiriarte, Heather Sams, Clarence Crucian, Brian E Feinberg, Andrew P Evaluation of techniques for performing cellular isolation and preservation during microgravity conditions |
title | Evaluation of techniques for performing cellular isolation and preservation during microgravity conditions |
title_full | Evaluation of techniques for performing cellular isolation and preservation during microgravity conditions |
title_fullStr | Evaluation of techniques for performing cellular isolation and preservation during microgravity conditions |
title_full_unstemmed | Evaluation of techniques for performing cellular isolation and preservation during microgravity conditions |
title_short | Evaluation of techniques for performing cellular isolation and preservation during microgravity conditions |
title_sort | evaluation of techniques for performing cellular isolation and preservation during microgravity conditions |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5515526/ https://www.ncbi.nlm.nih.gov/pubmed/28725735 http://dx.doi.org/10.1038/npjmgrav.2016.25 |
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