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Highly efficient cellular cloning using Ferro-core Micropallet Arrays

Advancing knowledge of biological mechanisms has come to depend upon genetic manipulation of cells and organisms, relying upon cellular cloning methods that remain unchanged for decades, are labor and time intensive, often taking many months to come to fruition. Thus, there is a pressing need for mo...

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Autores principales: Westerhof, Trisha M., Cox-Muranami, Wesley A., Li, Guann-Pyng, Bachman, Mark, Fan, Hung, Nelson, Edward L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5638909/
https://www.ncbi.nlm.nih.gov/pubmed/29026113
http://dx.doi.org/10.1038/s41598-017-13242-1
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author Westerhof, Trisha M.
Cox-Muranami, Wesley A.
Li, Guann-Pyng
Bachman, Mark
Fan, Hung
Nelson, Edward L.
author_facet Westerhof, Trisha M.
Cox-Muranami, Wesley A.
Li, Guann-Pyng
Bachman, Mark
Fan, Hung
Nelson, Edward L.
author_sort Westerhof, Trisha M.
collection PubMed
description Advancing knowledge of biological mechanisms has come to depend upon genetic manipulation of cells and organisms, relying upon cellular cloning methods that remain unchanged for decades, are labor and time intensive, often taking many months to come to fruition. Thus, there is a pressing need for more efficient processes. We have adapted a newly developed micropallet array platform, termed the “ferro-core micropallet array”, to dramatically improve and accelerate the process of isolating clonal populations of adherent cells from heterogeneous mixtures retaining the flexibility of employing a wide range of cytometric parameters for identifying colonies and cells of interest. Using transfected (retroviral oncogene or fluorescent reporter construct) rat 208 F cells, we demonstrated the capacity to isolate and expand pure populations of genetically manipulated cells via laser release and magnetic recovery of single micropallets carrying adherent microcolonies derived from single cells. This platform can be broadly applied to biological research, across the spectrum of molecular biology to cellular biology, involving fields such as cancer, developmental, and stem cell biology. The ferro-core micropallet array platform provides significant advantages over alternative sorting and cloning methods by eliminating the necessity for repetitive purification steps and increasing throughput by dramatically shortening the time to obtain clonally expanded cell colonies.
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spelling pubmed-56389092017-10-18 Highly efficient cellular cloning using Ferro-core Micropallet Arrays Westerhof, Trisha M. Cox-Muranami, Wesley A. Li, Guann-Pyng Bachman, Mark Fan, Hung Nelson, Edward L. Sci Rep Article Advancing knowledge of biological mechanisms has come to depend upon genetic manipulation of cells and organisms, relying upon cellular cloning methods that remain unchanged for decades, are labor and time intensive, often taking many months to come to fruition. Thus, there is a pressing need for more efficient processes. We have adapted a newly developed micropallet array platform, termed the “ferro-core micropallet array”, to dramatically improve and accelerate the process of isolating clonal populations of adherent cells from heterogeneous mixtures retaining the flexibility of employing a wide range of cytometric parameters for identifying colonies and cells of interest. Using transfected (retroviral oncogene or fluorescent reporter construct) rat 208 F cells, we demonstrated the capacity to isolate and expand pure populations of genetically manipulated cells via laser release and magnetic recovery of single micropallets carrying adherent microcolonies derived from single cells. This platform can be broadly applied to biological research, across the spectrum of molecular biology to cellular biology, involving fields such as cancer, developmental, and stem cell biology. The ferro-core micropallet array platform provides significant advantages over alternative sorting and cloning methods by eliminating the necessity for repetitive purification steps and increasing throughput by dramatically shortening the time to obtain clonally expanded cell colonies. Nature Publishing Group UK 2017-10-12 /pmc/articles/PMC5638909/ /pubmed/29026113 http://dx.doi.org/10.1038/s41598-017-13242-1 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Westerhof, Trisha M.
Cox-Muranami, Wesley A.
Li, Guann-Pyng
Bachman, Mark
Fan, Hung
Nelson, Edward L.
Highly efficient cellular cloning using Ferro-core Micropallet Arrays
title Highly efficient cellular cloning using Ferro-core Micropallet Arrays
title_full Highly efficient cellular cloning using Ferro-core Micropallet Arrays
title_fullStr Highly efficient cellular cloning using Ferro-core Micropallet Arrays
title_full_unstemmed Highly efficient cellular cloning using Ferro-core Micropallet Arrays
title_short Highly efficient cellular cloning using Ferro-core Micropallet Arrays
title_sort highly efficient cellular cloning using ferro-core micropallet arrays
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5638909/
https://www.ncbi.nlm.nih.gov/pubmed/29026113
http://dx.doi.org/10.1038/s41598-017-13242-1
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