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Cytokine-release kinetics of platelet-rich plasma according to various activation protocols

OBJECTIVES: This study was conducted to evaluate the cytokine-release kinetics of platelet-rich plasma (PRP) according to different activation protocols. METHODS: Two manual preparation procedures (single-spin (SS) at 900 g for five minutes; double-spin (DS) at 900 g for five minutes and then 1500 g...

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Autores principales: Roh, Y. H., Kim, W., Park, K. U., Oh, J. H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4852788/
https://www.ncbi.nlm.nih.gov/pubmed/26862077
http://dx.doi.org/10.1302/2046-3758.52.2000540
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author Roh, Y. H.
Kim, W.
Park, K. U.
Oh, J. H.
author_facet Roh, Y. H.
Kim, W.
Park, K. U.
Oh, J. H.
author_sort Roh, Y. H.
collection PubMed
description OBJECTIVES: This study was conducted to evaluate the cytokine-release kinetics of platelet-rich plasma (PRP) according to different activation protocols. METHODS: Two manual preparation procedures (single-spin (SS) at 900 g for five minutes; double-spin (DS) at 900 g for five minutes and then 1500 g for 15 minutes) were performed for each of 14 healthy subjects. Both preparations were tested for platelet activation by one of three activation protocols: no activation, activation with calcium (Ca) only, or calcium with a low dose (50 IU per 1 ml PRP) of thrombin. Each preparation was divided into four aliquots and incubated for one hour, 24 hours, 72 hours, and seven days. The cytokine-release kinetics were evaluated by assessing PDGF, TGF, VEGF, FGF, IL-1, and MMP-9 concentrations with bead-based sandwich immunoassay. RESULTS: The concentration of cytokine released from PRP varied over time and was influenced by various activation protocols. Ca-only activation had a significant effect on the DS PRPs (where the VEGF, FGF, and IL-1 concentrations were sustained) while Ca/thrombin activation had effects on both SS and DS PRPs (where the PDGF and VEGF concentrations were sustained and the TGF and FGF concentrations were short). The IL-1 content showed a significant increase with Ca-only or Ca/thrombin activation while these activations did not increase the MMP-9 concentration. CONCLUSION: The SS and DS methods differed in their effect on cytokine release, and this effect varied among the cytokines analysed. In addition, low dose of thrombin/calcium activation increased the overall cytokine release of the PRP preparations over seven days, relative to that with a calcium-only supplement or non-activation. Cite this article: Professor J. H. Oh. Cytokine-release kinetics of platelet-rich plasma according to various activation protocols. Bone Joint Res 2016;5:37–45. DOI: 10.1302/2046-3758.52.2000540
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spelling pubmed-48527882016-05-11 Cytokine-release kinetics of platelet-rich plasma according to various activation protocols Roh, Y. H. Kim, W. Park, K. U. Oh, J. H. Bone Joint Res Research OBJECTIVES: This study was conducted to evaluate the cytokine-release kinetics of platelet-rich plasma (PRP) according to different activation protocols. METHODS: Two manual preparation procedures (single-spin (SS) at 900 g for five minutes; double-spin (DS) at 900 g for five minutes and then 1500 g for 15 minutes) were performed for each of 14 healthy subjects. Both preparations were tested for platelet activation by one of three activation protocols: no activation, activation with calcium (Ca) only, or calcium with a low dose (50 IU per 1 ml PRP) of thrombin. Each preparation was divided into four aliquots and incubated for one hour, 24 hours, 72 hours, and seven days. The cytokine-release kinetics were evaluated by assessing PDGF, TGF, VEGF, FGF, IL-1, and MMP-9 concentrations with bead-based sandwich immunoassay. RESULTS: The concentration of cytokine released from PRP varied over time and was influenced by various activation protocols. Ca-only activation had a significant effect on the DS PRPs (where the VEGF, FGF, and IL-1 concentrations were sustained) while Ca/thrombin activation had effects on both SS and DS PRPs (where the PDGF and VEGF concentrations were sustained and the TGF and FGF concentrations were short). The IL-1 content showed a significant increase with Ca-only or Ca/thrombin activation while these activations did not increase the MMP-9 concentration. CONCLUSION: The SS and DS methods differed in their effect on cytokine release, and this effect varied among the cytokines analysed. In addition, low dose of thrombin/calcium activation increased the overall cytokine release of the PRP preparations over seven days, relative to that with a calcium-only supplement or non-activation. Cite this article: Professor J. H. Oh. Cytokine-release kinetics of platelet-rich plasma according to various activation protocols. Bone Joint Res 2016;5:37–45. DOI: 10.1302/2046-3758.52.2000540 2016-04-08 /pmc/articles/PMC4852788/ /pubmed/26862077 http://dx.doi.org/10.1302/2046-3758.52.2000540 Text en © 2016 Oh et al. This is an open-access article distributed under the terms of the Creative Commons Attributions licence (CC-BY-NC), which permits unrestricted use, distribution, and reproduction in any medium, but not for commercial gain, provided the original author and source are credited.
spellingShingle Research
Roh, Y. H.
Kim, W.
Park, K. U.
Oh, J. H.
Cytokine-release kinetics of platelet-rich plasma according to various activation protocols
title Cytokine-release kinetics of platelet-rich plasma according to various activation protocols
title_full Cytokine-release kinetics of platelet-rich plasma according to various activation protocols
title_fullStr Cytokine-release kinetics of platelet-rich plasma according to various activation protocols
title_full_unstemmed Cytokine-release kinetics of platelet-rich plasma according to various activation protocols
title_short Cytokine-release kinetics of platelet-rich plasma according to various activation protocols
title_sort cytokine-release kinetics of platelet-rich plasma according to various activation protocols
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4852788/
https://www.ncbi.nlm.nih.gov/pubmed/26862077
http://dx.doi.org/10.1302/2046-3758.52.2000540
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