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Periosteum and fascia lata: Are they so different?

Introduction: The human fascia lata (HFL) is used widely in reconstructive surgery in indications other than fracture repair. The goal of this study was to compare microscopic, molecular, and mechanical properties of HFL and periosteum (HP) from a bone tissue engineering perspective. Material and Me...

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Autores principales: Manon, Julie, Evrard, Robin, Maistriaux, Louis, Fievé, Lies, Heller, Ugo, Magnin, Delphine, Boisson, Jean, Kadlub, Natacha, Schubert, Thomas, Lengelé, Benoît, Behets, Catherine, Cornu, Olivier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9627508/
https://www.ncbi.nlm.nih.gov/pubmed/36338112
http://dx.doi.org/10.3389/fbioe.2022.944828
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author Manon, Julie
Evrard, Robin
Maistriaux, Louis
Fievé, Lies
Heller, Ugo
Magnin, Delphine
Boisson, Jean
Kadlub, Natacha
Schubert, Thomas
Lengelé, Benoît
Behets, Catherine
Cornu, Olivier
author_facet Manon, Julie
Evrard, Robin
Maistriaux, Louis
Fievé, Lies
Heller, Ugo
Magnin, Delphine
Boisson, Jean
Kadlub, Natacha
Schubert, Thomas
Lengelé, Benoît
Behets, Catherine
Cornu, Olivier
author_sort Manon, Julie
collection PubMed
description Introduction: The human fascia lata (HFL) is used widely in reconstructive surgery in indications other than fracture repair. The goal of this study was to compare microscopic, molecular, and mechanical properties of HFL and periosteum (HP) from a bone tissue engineering perspective. Material and Methods: Cadaveric HP and HFL (N = 4 each) microscopic morphology was characterized using histology and immunohistochemistry (IHC), and the extracellular matrix (ECM) ultrastructure assessed by means of scanning electron microscopy (SEM). DNA, collagen, elastin, glycosaminoglycans, major histocompatibility complex Type 1, and bone morphogenetic protein (BMP) contents were quantified. HP (N = 6) and HFL (N = 11) were submitted to stretch tests. Results: Histology and IHC highlighted similarities (Type I collagen fibers and two-layer organization) but also differences (fiber thickness and compaction and cell type) between both tissues, as confirmed using SEM. The collagen content was statistically higher in HFL than HP (735 vs. 160.2 μg/mg dry weight, respectively, p < 0.0001). On the contrary, DNA content was lower in HFL than HP (404.75 vs. 1,102.2 μg/mg dry weight, respectively, p = 0.0032), as was the immunogenic potential (p = 0.0033). BMP-2 and BMP-7 contents did not differ between both tissues (p = 0.132 and p = 0.699, respectively). HFL supported a significantly higher tension stress than HP. Conclusion: HP and HFL display morphological differences, despite their similar molecular ECM components. The stronger stretching resistance of HFL can specifically be explained by its higher collagen content. However, HFL contains many fewer cells and is less immunogenic than HP, as latter is rich in periosteal stem cells. In conclusion, HFL is likely suitable to replace HP architecture to confer a guide for bone consolidation, with an absence of osteogenicity. This study could pave the way to a bio-engineered periosteum built from HFL.
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spelling pubmed-96275082022-11-03 Periosteum and fascia lata: Are they so different? Manon, Julie Evrard, Robin Maistriaux, Louis Fievé, Lies Heller, Ugo Magnin, Delphine Boisson, Jean Kadlub, Natacha Schubert, Thomas Lengelé, Benoît Behets, Catherine Cornu, Olivier Front Bioeng Biotechnol Bioengineering and Biotechnology Introduction: The human fascia lata (HFL) is used widely in reconstructive surgery in indications other than fracture repair. The goal of this study was to compare microscopic, molecular, and mechanical properties of HFL and periosteum (HP) from a bone tissue engineering perspective. Material and Methods: Cadaveric HP and HFL (N = 4 each) microscopic morphology was characterized using histology and immunohistochemistry (IHC), and the extracellular matrix (ECM) ultrastructure assessed by means of scanning electron microscopy (SEM). DNA, collagen, elastin, glycosaminoglycans, major histocompatibility complex Type 1, and bone morphogenetic protein (BMP) contents were quantified. HP (N = 6) and HFL (N = 11) were submitted to stretch tests. Results: Histology and IHC highlighted similarities (Type I collagen fibers and two-layer organization) but also differences (fiber thickness and compaction and cell type) between both tissues, as confirmed using SEM. The collagen content was statistically higher in HFL than HP (735 vs. 160.2 μg/mg dry weight, respectively, p < 0.0001). On the contrary, DNA content was lower in HFL than HP (404.75 vs. 1,102.2 μg/mg dry weight, respectively, p = 0.0032), as was the immunogenic potential (p = 0.0033). BMP-2 and BMP-7 contents did not differ between both tissues (p = 0.132 and p = 0.699, respectively). HFL supported a significantly higher tension stress than HP. Conclusion: HP and HFL display morphological differences, despite their similar molecular ECM components. The stronger stretching resistance of HFL can specifically be explained by its higher collagen content. However, HFL contains many fewer cells and is less immunogenic than HP, as latter is rich in periosteal stem cells. In conclusion, HFL is likely suitable to replace HP architecture to confer a guide for bone consolidation, with an absence of osteogenicity. This study could pave the way to a bio-engineered periosteum built from HFL. Frontiers Media S.A. 2022-10-19 /pmc/articles/PMC9627508/ /pubmed/36338112 http://dx.doi.org/10.3389/fbioe.2022.944828 Text en Copyright © 2022 Manon, Evrard, Maistriaux, Fievé, Heller, Magnin, Boisson, Kadlub, Schubert, Lengelé, Behets and Cornu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Bioengineering and Biotechnology
Manon, Julie
Evrard, Robin
Maistriaux, Louis
Fievé, Lies
Heller, Ugo
Magnin, Delphine
Boisson, Jean
Kadlub, Natacha
Schubert, Thomas
Lengelé, Benoît
Behets, Catherine
Cornu, Olivier
Periosteum and fascia lata: Are they so different?
title Periosteum and fascia lata: Are they so different?
title_full Periosteum and fascia lata: Are they so different?
title_fullStr Periosteum and fascia lata: Are they so different?
title_full_unstemmed Periosteum and fascia lata: Are they so different?
title_short Periosteum and fascia lata: Are they so different?
title_sort periosteum and fascia lata: are they so different?
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9627508/
https://www.ncbi.nlm.nih.gov/pubmed/36338112
http://dx.doi.org/10.3389/fbioe.2022.944828
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