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The evaluation of leukocyte-platelet rich fibrin as an anti-inflammatory autologous biological additive: A novel in vitro study

OBJECTIVES: To investigate the use of leukocyte-platelet rich fibrin on suppressing the porphyromonas gingivalis (PG-LPS)-induced secretion of proinflammatory cytokines. METHODS: This quantitative experimental study was conducted at the School and Hospital of Stomatology, Jilin University, Changchun...

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Detalles Bibliográficos
Autores principales: Mudalal, Mahmoud, Sun, Xiaolin, Li, Xue, Zhou, Yanmin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Saudi Medical Journal 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6757208/
https://www.ncbi.nlm.nih.gov/pubmed/31287125
http://dx.doi.org/10.15537/smj.2019.7.24302
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author Mudalal, Mahmoud
Sun, Xiaolin
Li, Xue
Zhou, Yanmin
author_facet Mudalal, Mahmoud
Sun, Xiaolin
Li, Xue
Zhou, Yanmin
author_sort Mudalal, Mahmoud
collection PubMed
description OBJECTIVES: To investigate the use of leukocyte-platelet rich fibrin on suppressing the porphyromonas gingivalis (PG-LPS)-induced secretion of proinflammatory cytokines. METHODS: This quantitative experimental study was conducted at the School and Hospital of Stomatology, Jilin University, Changchun, China, between September 2017 and January 2019. A modified technique was used to obtain human gingival fibroblast cells (HGFCs). 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) and Cell Counting Kit-8 tests were established to determine the proliferation rate. Human gingival fibroblast cells were treated by PG-LPS at different periods and the isolated mRNA was subjected to reverse transcription polymerase chain reaction and real time quantitative polymerase chain reaction. The release of platelet-derived growth factor and transforming-growth factor-β1 at various time intervals was observed. RESULTS: We successfully established a modified technique for the production of HGFCs culture. One µg/mL PG-LPS was the recommended concentration to inhibit fibroblast proliferation. The expression of the pro-inflammatory cytokines messenger ribnucleic acid was notably raised at 3 and 6 hours post-PG-LPS treatment. The cumulative release of growth factors peaked during the first 24 hours and the production continued for 10 days. However, the fibroblast expression of cytokines was significantly suppressed after treatment with leucocyte- and platelet-rich fibrin (L-PRF). CONCLUSION: This study provided a novel way of obtaining HGFCs and greater understanding of the clinical impacts through the assessment of the anti-inflammatory properties of L-PRF in vitro.
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spelling pubmed-67572082021-02-26 The evaluation of leukocyte-platelet rich fibrin as an anti-inflammatory autologous biological additive: A novel in vitro study Mudalal, Mahmoud Sun, Xiaolin Li, Xue Zhou, Yanmin Saudi Med J Original Article OBJECTIVES: To investigate the use of leukocyte-platelet rich fibrin on suppressing the porphyromonas gingivalis (PG-LPS)-induced secretion of proinflammatory cytokines. METHODS: This quantitative experimental study was conducted at the School and Hospital of Stomatology, Jilin University, Changchun, China, between September 2017 and January 2019. A modified technique was used to obtain human gingival fibroblast cells (HGFCs). 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) and Cell Counting Kit-8 tests were established to determine the proliferation rate. Human gingival fibroblast cells were treated by PG-LPS at different periods and the isolated mRNA was subjected to reverse transcription polymerase chain reaction and real time quantitative polymerase chain reaction. The release of platelet-derived growth factor and transforming-growth factor-β1 at various time intervals was observed. RESULTS: We successfully established a modified technique for the production of HGFCs culture. One µg/mL PG-LPS was the recommended concentration to inhibit fibroblast proliferation. The expression of the pro-inflammatory cytokines messenger ribnucleic acid was notably raised at 3 and 6 hours post-PG-LPS treatment. The cumulative release of growth factors peaked during the first 24 hours and the production continued for 10 days. However, the fibroblast expression of cytokines was significantly suppressed after treatment with leucocyte- and platelet-rich fibrin (L-PRF). CONCLUSION: This study provided a novel way of obtaining HGFCs and greater understanding of the clinical impacts through the assessment of the anti-inflammatory properties of L-PRF in vitro. Saudi Medical Journal 2019 /pmc/articles/PMC6757208/ /pubmed/31287125 http://dx.doi.org/10.15537/smj.2019.7.24302 Text en Copyright: © Saudi Medical Journal http://creativecommons.org/licenses/by-nc This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial License (CC BY-NC), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Mudalal, Mahmoud
Sun, Xiaolin
Li, Xue
Zhou, Yanmin
The evaluation of leukocyte-platelet rich fibrin as an anti-inflammatory autologous biological additive: A novel in vitro study
title The evaluation of leukocyte-platelet rich fibrin as an anti-inflammatory autologous biological additive: A novel in vitro study
title_full The evaluation of leukocyte-platelet rich fibrin as an anti-inflammatory autologous biological additive: A novel in vitro study
title_fullStr The evaluation of leukocyte-platelet rich fibrin as an anti-inflammatory autologous biological additive: A novel in vitro study
title_full_unstemmed The evaluation of leukocyte-platelet rich fibrin as an anti-inflammatory autologous biological additive: A novel in vitro study
title_short The evaluation of leukocyte-platelet rich fibrin as an anti-inflammatory autologous biological additive: A novel in vitro study
title_sort evaluation of leukocyte-platelet rich fibrin as an anti-inflammatory autologous biological additive: a novel in vitro study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6757208/
https://www.ncbi.nlm.nih.gov/pubmed/31287125
http://dx.doi.org/10.15537/smj.2019.7.24302
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