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Peripheral mononuclear blood cell apheresis in a preclinical ovine model

BACKGROUND: Recent research has demonstrated that circulating peripheral blood mononuclear fractions (PBMC) containing haematopoietic stem (HSC)/progenitor cells have the potential to play a crucial role in regenerative medicine strategies. Work in our laboratory has shown that a peripheral blood mo...

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Autores principales: Lydon, Helen, Brooks, Roger, McCaskie, Andrew, Henson, Frances
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5812194/
https://www.ncbi.nlm.nih.gov/pubmed/29439735
http://dx.doi.org/10.1186/s12917-018-1332-4
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author Lydon, Helen
Brooks, Roger
McCaskie, Andrew
Henson, Frances
author_facet Lydon, Helen
Brooks, Roger
McCaskie, Andrew
Henson, Frances
author_sort Lydon, Helen
collection PubMed
description BACKGROUND: Recent research has demonstrated that circulating peripheral blood mononuclear fractions (PBMC) containing haematopoietic stem (HSC)/progenitor cells have the potential to play a crucial role in regenerative medicine strategies. Work in our laboratory has shown that a peripheral blood mononuclear cell fraction (PBMC) enhances cartilage repair in an osteochondral defect model in sheep and has a significant effect on cells in the joint niche. In order to obtain PBMC rich blood containing HSCs for further studies, we have performed, for the first time, apheresis on adult sheep. RESULTS: Subcutaneous granulocyte-colony stimulating factor (G-CSF) was used to mobilise white blood cells and continual flow apheresis was performed on 8 sheep under general anaesthetic. There were no observable side effects, although a marked tendency for blood clotting during the procedure was noted. The administration of G-CSF for 3 days increased the white blood cell (WBC) count in the peripheral blood from to 6.7 ± 2.1 × 10(6)/ml to 16.1 ± 5.0 × 10(6)/ml. Following apheresis, the WBC numbers in the apheretic product increased to 38.5 ± 27.6 × 10(6)/ml, comprised of a significant increase in neutrophils and PBMC (from 5.25 ± 1.8 × 10(6)/ml following G-CSF stimulation to 27.5 5 ± 27.6 × 10(6)/ml). There was a mean of 2.1% CD34 + ve cells and 95.5% CD45 + ve cells in the apheretic product. CONCLUSIONS: This study describes the administration of G-CSF and subsequent apheresis in adult sheep. The technique is safe when performed as described with no observable side effects. The technique permits collection of an increased WBC fraction containing neutrophils and PBMC in adult sheep. This apheretic product contains CD34 + ve cells, representing an HSC/progenitor population for use in in vivo and in vitro experiments.
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spelling pubmed-58121942018-02-15 Peripheral mononuclear blood cell apheresis in a preclinical ovine model Lydon, Helen Brooks, Roger McCaskie, Andrew Henson, Frances BMC Vet Res Research Article BACKGROUND: Recent research has demonstrated that circulating peripheral blood mononuclear fractions (PBMC) containing haematopoietic stem (HSC)/progenitor cells have the potential to play a crucial role in regenerative medicine strategies. Work in our laboratory has shown that a peripheral blood mononuclear cell fraction (PBMC) enhances cartilage repair in an osteochondral defect model in sheep and has a significant effect on cells in the joint niche. In order to obtain PBMC rich blood containing HSCs for further studies, we have performed, for the first time, apheresis on adult sheep. RESULTS: Subcutaneous granulocyte-colony stimulating factor (G-CSF) was used to mobilise white blood cells and continual flow apheresis was performed on 8 sheep under general anaesthetic. There were no observable side effects, although a marked tendency for blood clotting during the procedure was noted. The administration of G-CSF for 3 days increased the white blood cell (WBC) count in the peripheral blood from to 6.7 ± 2.1 × 10(6)/ml to 16.1 ± 5.0 × 10(6)/ml. Following apheresis, the WBC numbers in the apheretic product increased to 38.5 ± 27.6 × 10(6)/ml, comprised of a significant increase in neutrophils and PBMC (from 5.25 ± 1.8 × 10(6)/ml following G-CSF stimulation to 27.5 5 ± 27.6 × 10(6)/ml). There was a mean of 2.1% CD34 + ve cells and 95.5% CD45 + ve cells in the apheretic product. CONCLUSIONS: This study describes the administration of G-CSF and subsequent apheresis in adult sheep. The technique is safe when performed as described with no observable side effects. The technique permits collection of an increased WBC fraction containing neutrophils and PBMC in adult sheep. This apheretic product contains CD34 + ve cells, representing an HSC/progenitor population for use in in vivo and in vitro experiments. BioMed Central 2018-02-13 /pmc/articles/PMC5812194/ /pubmed/29439735 http://dx.doi.org/10.1186/s12917-018-1332-4 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Lydon, Helen
Brooks, Roger
McCaskie, Andrew
Henson, Frances
Peripheral mononuclear blood cell apheresis in a preclinical ovine model
title Peripheral mononuclear blood cell apheresis in a preclinical ovine model
title_full Peripheral mononuclear blood cell apheresis in a preclinical ovine model
title_fullStr Peripheral mononuclear blood cell apheresis in a preclinical ovine model
title_full_unstemmed Peripheral mononuclear blood cell apheresis in a preclinical ovine model
title_short Peripheral mononuclear blood cell apheresis in a preclinical ovine model
title_sort peripheral mononuclear blood cell apheresis in a preclinical ovine model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5812194/
https://www.ncbi.nlm.nih.gov/pubmed/29439735
http://dx.doi.org/10.1186/s12917-018-1332-4
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