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Collection and processing of whole blood for transformation of peripheral blood mononuclear cells and extraction of DNA: the Type 1 Diabetes Genetics Consortium

Background and Purpose To yield large amounts of DNA for many genotype analyses and to provide a renewable source of DNA, the Type 1 Diabetes Genetics Consortium (T1DGC) harvested DNA and peripheral blood mononuclear cells (PBMCs) from individuals with type 1 diabetes and their family members in sev...

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Autores principales: Rosinger, Silke, Nutland, Sarah, Mickelson, Eric, Varney, Michael D, Boehm, Bernard O, Olsem, Gary J, Hansen, John A, Nicholson, Ian, Hilner, Joan E, Perdue, Letitia H, Pierce, June J, Akolkar, Beena, Nierras, Concepcion, Steffes, Michael W
Formato: Texto
Lenguaje:English
Publicado: SAGE Publications 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2917848/
https://www.ncbi.nlm.nih.gov/pubmed/20595244
http://dx.doi.org/10.1177/1740774510373493
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author Rosinger, Silke
Nutland, Sarah
Mickelson, Eric
Varney, Michael D
Boehm, Bernard O
Olsem, Gary J
Hansen, John A
Nicholson, Ian
Hilner, Joan E
Perdue, Letitia H
Pierce, June J
Akolkar, Beena
Nierras, Concepcion
Steffes, Michael W
author_facet Rosinger, Silke
Nutland, Sarah
Mickelson, Eric
Varney, Michael D
Boehm, Bernard O
Olsem, Gary J
Hansen, John A
Nicholson, Ian
Hilner, Joan E
Perdue, Letitia H
Pierce, June J
Akolkar, Beena
Nierras, Concepcion
Steffes, Michael W
author_sort Rosinger, Silke
collection PubMed
description Background and Purpose To yield large amounts of DNA for many genotype analyses and to provide a renewable source of DNA, the Type 1 Diabetes Genetics Consortium (T1DGC) harvested DNA and peripheral blood mononuclear cells (PBMCs) from individuals with type 1 diabetes and their family members in several regions of the world. Methods DNA repositories were established in Asia-Pacific, Europe, North America, and the United Kingdom. To address region-specific needs, different methods and sample processing techniques were used among the laboratories to extract and to quantify DNA and to establish Epstein-Barr virus transformed cell lines. Results More than 98% of the samples of PBMCs were successfully transformed. Approximately 20–25 µg of DNA were extracted per mL of whole blood. Extraction of DNA from the cell pack ranged from 92 to 165 µg per cell pack. In addition, the extracted DNA from whole blood or transformed cells was successfully utilized in each regional human leukocyte antigen genotyping laboratory and by several additional laboratories performing consortium-wide genotyping projects. Limitations Although the isolation of PBMCs was consistent among sites, the measurement of DNA was difficult to harmonize. Conclusions DNA repositories can be established in different regions of the world and produce similar amounts of high-quality DNA for a variety of high-throughput genotyping techniques. Furthermore, even with the distances and time necessary for transportation, highly efficient transformation of PBMCs is possible. For future studies/trials involving several laboratories in different locations, the T1DGC experience includes examples of protocols that may be applicable. In summary, T1DGC has developed protocols that would be of interest to any scientific organization attempting to overcome the logistical problems associated with studies/trials spanning multiple research facilities, located in different regions of the world.
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spelling pubmed-29178482010-08-13 Collection and processing of whole blood for transformation of peripheral blood mononuclear cells and extraction of DNA: the Type 1 Diabetes Genetics Consortium Rosinger, Silke Nutland, Sarah Mickelson, Eric Varney, Michael D Boehm, Bernard O Olsem, Gary J Hansen, John A Nicholson, Ian Hilner, Joan E Perdue, Letitia H Pierce, June J Akolkar, Beena Nierras, Concepcion Steffes, Michael W Clin Trials Articles Background and Purpose To yield large amounts of DNA for many genotype analyses and to provide a renewable source of DNA, the Type 1 Diabetes Genetics Consortium (T1DGC) harvested DNA and peripheral blood mononuclear cells (PBMCs) from individuals with type 1 diabetes and their family members in several regions of the world. Methods DNA repositories were established in Asia-Pacific, Europe, North America, and the United Kingdom. To address region-specific needs, different methods and sample processing techniques were used among the laboratories to extract and to quantify DNA and to establish Epstein-Barr virus transformed cell lines. Results More than 98% of the samples of PBMCs were successfully transformed. Approximately 20–25 µg of DNA were extracted per mL of whole blood. Extraction of DNA from the cell pack ranged from 92 to 165 µg per cell pack. In addition, the extracted DNA from whole blood or transformed cells was successfully utilized in each regional human leukocyte antigen genotyping laboratory and by several additional laboratories performing consortium-wide genotyping projects. Limitations Although the isolation of PBMCs was consistent among sites, the measurement of DNA was difficult to harmonize. Conclusions DNA repositories can be established in different regions of the world and produce similar amounts of high-quality DNA for a variety of high-throughput genotyping techniques. Furthermore, even with the distances and time necessary for transportation, highly efficient transformation of PBMCs is possible. For future studies/trials involving several laboratories in different locations, the T1DGC experience includes examples of protocols that may be applicable. In summary, T1DGC has developed protocols that would be of interest to any scientific organization attempting to overcome the logistical problems associated with studies/trials spanning multiple research facilities, located in different regions of the world. SAGE Publications 2010-08 /pmc/articles/PMC2917848/ /pubmed/20595244 http://dx.doi.org/10.1177/1740774510373493 Text en © The Author(s), 2010 http://creativecommons.org/licenses/by/2.0/ 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 work is properly cited.
spellingShingle Articles
Rosinger, Silke
Nutland, Sarah
Mickelson, Eric
Varney, Michael D
Boehm, Bernard O
Olsem, Gary J
Hansen, John A
Nicholson, Ian
Hilner, Joan E
Perdue, Letitia H
Pierce, June J
Akolkar, Beena
Nierras, Concepcion
Steffes, Michael W
Collection and processing of whole blood for transformation of peripheral blood mononuclear cells and extraction of DNA: the Type 1 Diabetes Genetics Consortium
title Collection and processing of whole blood for transformation of peripheral blood mononuclear cells and extraction of DNA: the Type 1 Diabetes Genetics Consortium
title_full Collection and processing of whole blood for transformation of peripheral blood mononuclear cells and extraction of DNA: the Type 1 Diabetes Genetics Consortium
title_fullStr Collection and processing of whole blood for transformation of peripheral blood mononuclear cells and extraction of DNA: the Type 1 Diabetes Genetics Consortium
title_full_unstemmed Collection and processing of whole blood for transformation of peripheral blood mononuclear cells and extraction of DNA: the Type 1 Diabetes Genetics Consortium
title_short Collection and processing of whole blood for transformation of peripheral blood mononuclear cells and extraction of DNA: the Type 1 Diabetes Genetics Consortium
title_sort collection and processing of whole blood for transformation of peripheral blood mononuclear cells and extraction of dna: the type 1 diabetes genetics consortium
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2917848/
https://www.ncbi.nlm.nih.gov/pubmed/20595244
http://dx.doi.org/10.1177/1740774510373493
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