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Effects of platelet-rich plasma on human gingival fibroblast proliferation and migration in vitro

OBJECTIVE: This study evaluated the influence of platelet-rich plasma (PRP) on the behaviour of human gingival fibroblasts (hGFs), including fibroblast proliferation, migration and colony formation. METHODS: PRP was obtained from the human peripheral blood of a healthy volunteer and then was diluted...

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Autores principales: NGUYEN, Phuc Anh, PHAM, Thuy Anh Vu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Faculdade De Odontologia De Bauru - USP 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6025888/
https://www.ncbi.nlm.nih.gov/pubmed/29995149
http://dx.doi.org/10.1590/1678-7757-2018-0077
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author NGUYEN, Phuc Anh
PHAM, Thuy Anh Vu
author_facet NGUYEN, Phuc Anh
PHAM, Thuy Anh Vu
author_sort NGUYEN, Phuc Anh
collection PubMed
description OBJECTIVE: This study evaluated the influence of platelet-rich plasma (PRP) on the behaviour of human gingival fibroblasts (hGFs), including fibroblast proliferation, migration and colony formation. METHODS: PRP was obtained from the human peripheral blood of a healthy volunteer and then was diluted into platelet concentrations of 1%, 2% and 5%. The proliferation of hGFs was determined by two methods: (1) Cell-number counting with a haemocytometer method at days 1, 3, 5 and 7; (2) Colony-forming unit-fibroblast (CFU-F) assay at 2 weeks. The migration of hGFs was evaluated with scratch assay, then recorded digital images were analysed by Image-Analysis J 1.51j8 software to compare the remaining artificial wound areas between PRP groups at 0, 24 and 48 hours. RESULTS: All hGFs that were cultivated in media with 1%, 2% and 5% PRP showed their ability to proliferate and migrate. Cell numbers incubated with 1% PRP increased significantly during the first three days and peaked at day 5, tending to be similar to their proliferation in complete medium. With concentrations of 2% and 5% PRP, hGFs outgrew and peaked at day 3, which was faster than with those in medium with 1% PRP. Especially, hGFs in the group 5% PRP proliferated with higher cell numbers than those in the other remaining groups at day 3. The hGF colony number that was formed in the group 5% PRP was significantly higher than those in the groups 1% and 2% PRP. Scratch assay showed hGFs in the groups 2% and 5% PRP almost filled the artificial wound and migrated more effectively than in the group 1% PRP at 24 hours, which was significant. CONCLUSION: In this study, perhaps the medium with 5% PRP is the dominant option, promoting the abilities of hGFs to heal wounds, because of its fast and effective impact on cell proliferation, colony formation and migration.
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spelling pubmed-60258882018-07-05 Effects of platelet-rich plasma on human gingival fibroblast proliferation and migration in vitro NGUYEN, Phuc Anh PHAM, Thuy Anh Vu J Appl Oral Sci Original Article OBJECTIVE: This study evaluated the influence of platelet-rich plasma (PRP) on the behaviour of human gingival fibroblasts (hGFs), including fibroblast proliferation, migration and colony formation. METHODS: PRP was obtained from the human peripheral blood of a healthy volunteer and then was diluted into platelet concentrations of 1%, 2% and 5%. The proliferation of hGFs was determined by two methods: (1) Cell-number counting with a haemocytometer method at days 1, 3, 5 and 7; (2) Colony-forming unit-fibroblast (CFU-F) assay at 2 weeks. The migration of hGFs was evaluated with scratch assay, then recorded digital images were analysed by Image-Analysis J 1.51j8 software to compare the remaining artificial wound areas between PRP groups at 0, 24 and 48 hours. RESULTS: All hGFs that were cultivated in media with 1%, 2% and 5% PRP showed their ability to proliferate and migrate. Cell numbers incubated with 1% PRP increased significantly during the first three days and peaked at day 5, tending to be similar to their proliferation in complete medium. With concentrations of 2% and 5% PRP, hGFs outgrew and peaked at day 3, which was faster than with those in medium with 1% PRP. Especially, hGFs in the group 5% PRP proliferated with higher cell numbers than those in the other remaining groups at day 3. The hGF colony number that was formed in the group 5% PRP was significantly higher than those in the groups 1% and 2% PRP. Scratch assay showed hGFs in the groups 2% and 5% PRP almost filled the artificial wound and migrated more effectively than in the group 1% PRP at 24 hours, which was significant. CONCLUSION: In this study, perhaps the medium with 5% PRP is the dominant option, promoting the abilities of hGFs to heal wounds, because of its fast and effective impact on cell proliferation, colony formation and migration. Faculdade De Odontologia De Bauru - USP 2018-06-25 /pmc/articles/PMC6025888/ /pubmed/29995149 http://dx.doi.org/10.1590/1678-7757-2018-0077 Text en https://creativecommons.org/licenses/by/4.0/ 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 Original Article
NGUYEN, Phuc Anh
PHAM, Thuy Anh Vu
Effects of platelet-rich plasma on human gingival fibroblast proliferation and migration in vitro
title Effects of platelet-rich plasma on human gingival fibroblast proliferation and migration in vitro
title_full Effects of platelet-rich plasma on human gingival fibroblast proliferation and migration in vitro
title_fullStr Effects of platelet-rich plasma on human gingival fibroblast proliferation and migration in vitro
title_full_unstemmed Effects of platelet-rich plasma on human gingival fibroblast proliferation and migration in vitro
title_short Effects of platelet-rich plasma on human gingival fibroblast proliferation and migration in vitro
title_sort effects of platelet-rich plasma on human gingival fibroblast proliferation and migration in vitro
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6025888/
https://www.ncbi.nlm.nih.gov/pubmed/29995149
http://dx.doi.org/10.1590/1678-7757-2018-0077
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