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Hypoxia as a Stimulus for the Maturation of Meniscal Cells: Highway to Novel Tissue Engineering Strategies?
The meniscus possesses low self-healing properties. A perfect regenerative technique for this tissue has not yet been developed. This work aims to evaluate the role of hypoxia in meniscal development in vitro. Menisci from neonatal pigs (day 0) were harvested and cultured under two different atmosph...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8267734/ https://www.ncbi.nlm.nih.gov/pubmed/34199089 http://dx.doi.org/10.3390/ijms22136905 |
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author | Herrera Millar, Valentina Rafaela Mangiavini, Laura Polito, Umberto Canciani, Barbara Nguyen, Van Thi Cirillo, Federica Anastasia, Luigi Peretti, Giuseppe Maria Modina, Silvia Clotilde Di Giancamillo, Alessia |
author_facet | Herrera Millar, Valentina Rafaela Mangiavini, Laura Polito, Umberto Canciani, Barbara Nguyen, Van Thi Cirillo, Federica Anastasia, Luigi Peretti, Giuseppe Maria Modina, Silvia Clotilde Di Giancamillo, Alessia |
author_sort | Herrera Millar, Valentina Rafaela |
collection | PubMed |
description | The meniscus possesses low self-healing properties. A perfect regenerative technique for this tissue has not yet been developed. This work aims to evaluate the role of hypoxia in meniscal development in vitro. Menisci from neonatal pigs (day 0) were harvested and cultured under two different atmospheric conditions: hypoxia (1% O(2)) and normoxia (21% O(2)) for up to 14 days. Samples were analysed at 0, 7 and 14 days by histochemical (Safranin-O staining), immunofluorescence and RT-PCR (in both methods for SOX-9, HIF-1α, collagen I and II), and biochemical (DNA, GAGs, DNA/GAGs ratio) techniques to record any possible differences in the maturation of meniscal cells. Safranin-O staining showed increments in matrix deposition and round-shape “fibro-chondrocytic” cells in hypoxia-cultured menisci compared with controls under normal atmospheric conditions. The same maturation shifting was observed by immunofluorescence and RT-PCR analysis: SOX-9 and collagen II increased from day zero up to 14 days under a hypoxic environment. An increment of DNA/GAGs ratio typical of mature meniscal tissue (characterized by fewer cells and more GAGs) was observed by biochemical analysis. This study shows that hypoxia can be considered as a booster to achieve meniscal cell maturation, and opens new opportunities in the field of meniscus tissue engineering. |
format | Online Article Text |
id | pubmed-8267734 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-82677342021-07-10 Hypoxia as a Stimulus for the Maturation of Meniscal Cells: Highway to Novel Tissue Engineering Strategies? Herrera Millar, Valentina Rafaela Mangiavini, Laura Polito, Umberto Canciani, Barbara Nguyen, Van Thi Cirillo, Federica Anastasia, Luigi Peretti, Giuseppe Maria Modina, Silvia Clotilde Di Giancamillo, Alessia Int J Mol Sci Article The meniscus possesses low self-healing properties. A perfect regenerative technique for this tissue has not yet been developed. This work aims to evaluate the role of hypoxia in meniscal development in vitro. Menisci from neonatal pigs (day 0) were harvested and cultured under two different atmospheric conditions: hypoxia (1% O(2)) and normoxia (21% O(2)) for up to 14 days. Samples were analysed at 0, 7 and 14 days by histochemical (Safranin-O staining), immunofluorescence and RT-PCR (in both methods for SOX-9, HIF-1α, collagen I and II), and biochemical (DNA, GAGs, DNA/GAGs ratio) techniques to record any possible differences in the maturation of meniscal cells. Safranin-O staining showed increments in matrix deposition and round-shape “fibro-chondrocytic” cells in hypoxia-cultured menisci compared with controls under normal atmospheric conditions. The same maturation shifting was observed by immunofluorescence and RT-PCR analysis: SOX-9 and collagen II increased from day zero up to 14 days under a hypoxic environment. An increment of DNA/GAGs ratio typical of mature meniscal tissue (characterized by fewer cells and more GAGs) was observed by biochemical analysis. This study shows that hypoxia can be considered as a booster to achieve meniscal cell maturation, and opens new opportunities in the field of meniscus tissue engineering. MDPI 2021-06-27 /pmc/articles/PMC8267734/ /pubmed/34199089 http://dx.doi.org/10.3390/ijms22136905 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Herrera Millar, Valentina Rafaela Mangiavini, Laura Polito, Umberto Canciani, Barbara Nguyen, Van Thi Cirillo, Federica Anastasia, Luigi Peretti, Giuseppe Maria Modina, Silvia Clotilde Di Giancamillo, Alessia Hypoxia as a Stimulus for the Maturation of Meniscal Cells: Highway to Novel Tissue Engineering Strategies? |
title | Hypoxia as a Stimulus for the Maturation of Meniscal Cells: Highway to Novel Tissue Engineering Strategies? |
title_full | Hypoxia as a Stimulus for the Maturation of Meniscal Cells: Highway to Novel Tissue Engineering Strategies? |
title_fullStr | Hypoxia as a Stimulus for the Maturation of Meniscal Cells: Highway to Novel Tissue Engineering Strategies? |
title_full_unstemmed | Hypoxia as a Stimulus for the Maturation of Meniscal Cells: Highway to Novel Tissue Engineering Strategies? |
title_short | Hypoxia as a Stimulus for the Maturation of Meniscal Cells: Highway to Novel Tissue Engineering Strategies? |
title_sort | hypoxia as a stimulus for the maturation of meniscal cells: highway to novel tissue engineering strategies? |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8267734/ https://www.ncbi.nlm.nih.gov/pubmed/34199089 http://dx.doi.org/10.3390/ijms22136905 |
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