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Human dermal fibroblast response to hyaluronic acid-based injectable dermal fillers: an in vitro study

INTRODUCTION: Hyaluronic acid (HA)-based injectable dermal fillers (IDFs) used in aesthetic procedures may increase fibroblast activity and ultimately improve subcutaneous tissue quality. AIM: To further our understanding of fibroblast response to different commercial HA-based IDFs. MATERIAL AND MET...

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Autores principales: Varì, Simona, Minoretti, Piercarlo, Emanuele, Enzo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9837592/
https://www.ncbi.nlm.nih.gov/pubmed/36686003
http://dx.doi.org/10.5114/ada.2022.114927
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author Varì, Simona
Minoretti, Piercarlo
Emanuele, Enzo
author_facet Varì, Simona
Minoretti, Piercarlo
Emanuele, Enzo
author_sort Varì, Simona
collection PubMed
description INTRODUCTION: Hyaluronic acid (HA)-based injectable dermal fillers (IDFs) used in aesthetic procedures may increase fibroblast activity and ultimately improve subcutaneous tissue quality. AIM: To further our understanding of fibroblast response to different commercial HA-based IDFs. MATERIAL AND METHODS: Normal human dermal fibroblasts (NHDFs) were cultured with four different commercially available HA-based IDFs to assess their effects on the synthesis of extracellular matrix components and regulators (type I collagen, type III collagen, elastin, and transforming growth factor (TGF)-β1) as well as pro-inflammatory and oxidative DNA damage markers (interleukin (IL)-1β and 8-hydroxy-2’-deoxyguanosine (8-OHdG)). The six biomarkers were measured in supernatants from NHDF cultures after 24 h, 48 h, and 72 h of exposure to HA-based IDFs. RESULTS: All tested IDFs elicited a higher release of type I collagen in NHDF culture supernatants, although Juvederm Voluma was found to induce the most pronounced increase. Agex Fill Ultra induced the highest production of type III collagen and elastin. Levels of TGF-β1 and type I collagen in cell culture supernatants were positively correlated to each other (r = 0.57, p < 0.05). Conversely, 8-OHdG concentrations were inversely associated with both type III collagen (r = –0.41, p < 0.05) and elastin (r = –0.46, p < 0.05). CONCLUSIONS: Commercially available HA-based IDFs may elicit different in vitro fibroblast responses – a finding with potential implications in the prediction of their effects in aesthetic procedures. Our results also confirm that in vitro experiments may be viable tools for testing the effects of HA-based IDFs without resorting to animal studies.
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spelling pubmed-98375922023-01-20 Human dermal fibroblast response to hyaluronic acid-based injectable dermal fillers: an in vitro study Varì, Simona Minoretti, Piercarlo Emanuele, Enzo Postepy Dermatol Alergol Original Paper INTRODUCTION: Hyaluronic acid (HA)-based injectable dermal fillers (IDFs) used in aesthetic procedures may increase fibroblast activity and ultimately improve subcutaneous tissue quality. AIM: To further our understanding of fibroblast response to different commercial HA-based IDFs. MATERIAL AND METHODS: Normal human dermal fibroblasts (NHDFs) were cultured with four different commercially available HA-based IDFs to assess their effects on the synthesis of extracellular matrix components and regulators (type I collagen, type III collagen, elastin, and transforming growth factor (TGF)-β1) as well as pro-inflammatory and oxidative DNA damage markers (interleukin (IL)-1β and 8-hydroxy-2’-deoxyguanosine (8-OHdG)). The six biomarkers were measured in supernatants from NHDF cultures after 24 h, 48 h, and 72 h of exposure to HA-based IDFs. RESULTS: All tested IDFs elicited a higher release of type I collagen in NHDF culture supernatants, although Juvederm Voluma was found to induce the most pronounced increase. Agex Fill Ultra induced the highest production of type III collagen and elastin. Levels of TGF-β1 and type I collagen in cell culture supernatants were positively correlated to each other (r = 0.57, p < 0.05). Conversely, 8-OHdG concentrations were inversely associated with both type III collagen (r = –0.41, p < 0.05) and elastin (r = –0.46, p < 0.05). CONCLUSIONS: Commercially available HA-based IDFs may elicit different in vitro fibroblast responses – a finding with potential implications in the prediction of their effects in aesthetic procedures. Our results also confirm that in vitro experiments may be viable tools for testing the effects of HA-based IDFs without resorting to animal studies. Termedia Publishing House 2022-04-01 2022-12 /pmc/articles/PMC9837592/ /pubmed/36686003 http://dx.doi.org/10.5114/ada.2022.114927 Text en Copyright: © 2022 Termedia Sp. z o. o. https://creativecommons.org/licenses/by-nc-sa/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
spellingShingle Original Paper
Varì, Simona
Minoretti, Piercarlo
Emanuele, Enzo
Human dermal fibroblast response to hyaluronic acid-based injectable dermal fillers: an in vitro study
title Human dermal fibroblast response to hyaluronic acid-based injectable dermal fillers: an in vitro study
title_full Human dermal fibroblast response to hyaluronic acid-based injectable dermal fillers: an in vitro study
title_fullStr Human dermal fibroblast response to hyaluronic acid-based injectable dermal fillers: an in vitro study
title_full_unstemmed Human dermal fibroblast response to hyaluronic acid-based injectable dermal fillers: an in vitro study
title_short Human dermal fibroblast response to hyaluronic acid-based injectable dermal fillers: an in vitro study
title_sort human dermal fibroblast response to hyaluronic acid-based injectable dermal fillers: an in vitro study
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9837592/
https://www.ncbi.nlm.nih.gov/pubmed/36686003
http://dx.doi.org/10.5114/ada.2022.114927
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