Porous 3D Scaffolds Enhance MSC Vitality and Reduce Osteoclast Activity

In the context of an aging population, unhealthy Western lifestyle, and the lack of an optimal surgical treatment, deep osteochondral defects pose a great challenge for the public health system. Biodegradable, biomimetic scaffolds seem to be a promising solution. In this study we investigated the bi...

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Main Authors: Miriam Spreda, Nicole Hauptmann, Veronika Lehner, Christoph Biehl, Klaus Liefeith, Katrin Susanne Lips
Format: Article
Language:English
Published: MDPI AG 2021-10-01
Series:Molecules
Subjects:
Online Access:https://www.mdpi.com/1420-3049/26/20/6258
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author Miriam Spreda
Nicole Hauptmann
Veronika Lehner
Christoph Biehl
Klaus Liefeith
Katrin Susanne Lips
author_facet Miriam Spreda
Nicole Hauptmann
Veronika Lehner
Christoph Biehl
Klaus Liefeith
Katrin Susanne Lips
author_sort Miriam Spreda
collection DOAJ
description In the context of an aging population, unhealthy Western lifestyle, and the lack of an optimal surgical treatment, deep osteochondral defects pose a great challenge for the public health system. Biodegradable, biomimetic scaffolds seem to be a promising solution. In this study we investigated the biocompatibility of porous poly-((D,L)-lactide-ε-caprolactone)dimethacrylate (LCM) scaffolds in contrast to compact LCM scaffolds and blank cell culture plastic. Thus, morphology, cytotoxicity and metabolic activity of human mesenchymal stromal cells (MSC) seeded directly on the materials were analyzed after three and six days of culturing. Further, osteoclastogenesis and osteoclastic activity were assessed using reverse-transcriptase real-time PCR of osteoclast-specific genes, EIA and morphologic aspects after four, eight, and twelve days. LCM scaffolds did not display cytotoxic effects on MSC. After three days, metabolic activity of MSC was enhanced on 3D porous scaffolds (PS) compared to 2D compact scaffolds (CS). Osteoclast activity seemed to be reduced at PS compared to cell culture plastic at all time points, while no differences in osteoclastogenesis were detectable between the materials. These results indicate a good cytocompatibility of LCM scaffolds. Interestingly, porous 3D structure induced higher metabolic activity of MSC as well as reduced osteoclast activity.
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spelling doaj.art-182271e977e44533aa5757c72ac1d8072023-11-22T19:20:31ZengMDPI AGMolecules1420-30492021-10-012620625810.3390/molecules26206258Porous 3D Scaffolds Enhance MSC Vitality and Reduce Osteoclast ActivityMiriam Spreda0Nicole Hauptmann1Veronika Lehner2Christoph Biehl3Klaus Liefeith4Katrin Susanne Lips5Experimental Trauma Surgery, Justus-Liebig-University Giessen, Aulweg 128, 35392 Giessen, GermanyDepartment of Biomaterials, Institute for Bioprocessing and Analytical Measurement Techniques e.V. (iba), Rosenhof, 37308 Heilbad Heiligenstadt, GermanyExperimental Trauma Surgery, Justus-Liebig-University Giessen, Aulweg 128, 35392 Giessen, GermanyDepartment of Trauma, Hand and Reconstructive Surgery, University Hospital of Giessen-Marburg GmbH, Campus Giessen, Rudolf-Buchheim-Strasse 7, 35392 Giessen, GermanyDepartment of Biomaterials, Institute for Bioprocessing and Analytical Measurement Techniques e.V. (iba), Rosenhof, 37308 Heilbad Heiligenstadt, GermanyExperimental Trauma Surgery, Justus-Liebig-University Giessen, Aulweg 128, 35392 Giessen, GermanyIn the context of an aging population, unhealthy Western lifestyle, and the lack of an optimal surgical treatment, deep osteochondral defects pose a great challenge for the public health system. Biodegradable, biomimetic scaffolds seem to be a promising solution. In this study we investigated the biocompatibility of porous poly-((D,L)-lactide-ε-caprolactone)dimethacrylate (LCM) scaffolds in contrast to compact LCM scaffolds and blank cell culture plastic. Thus, morphology, cytotoxicity and metabolic activity of human mesenchymal stromal cells (MSC) seeded directly on the materials were analyzed after three and six days of culturing. Further, osteoclastogenesis and osteoclastic activity were assessed using reverse-transcriptase real-time PCR of osteoclast-specific genes, EIA and morphologic aspects after four, eight, and twelve days. LCM scaffolds did not display cytotoxic effects on MSC. After three days, metabolic activity of MSC was enhanced on 3D porous scaffolds (PS) compared to 2D compact scaffolds (CS). Osteoclast activity seemed to be reduced at PS compared to cell culture plastic at all time points, while no differences in osteoclastogenesis were detectable between the materials. These results indicate a good cytocompatibility of LCM scaffolds. Interestingly, porous 3D structure induced higher metabolic activity of MSC as well as reduced osteoclast activity.https://www.mdpi.com/1420-3049/26/20/62583D-printingosteoclastsmesenchymal stromal cellstartrate-resistant acid phosphatasemRNA expressionimplant
spellingShingle Miriam Spreda
Nicole Hauptmann
Veronika Lehner
Christoph Biehl
Klaus Liefeith
Katrin Susanne Lips
Porous 3D Scaffolds Enhance MSC Vitality and Reduce Osteoclast Activity
Molecules
3D-printing
osteoclasts
mesenchymal stromal cells
tartrate-resistant acid phosphatase
mRNA expression
implant
title Porous 3D Scaffolds Enhance MSC Vitality and Reduce Osteoclast Activity
title_full Porous 3D Scaffolds Enhance MSC Vitality and Reduce Osteoclast Activity
title_fullStr Porous 3D Scaffolds Enhance MSC Vitality and Reduce Osteoclast Activity
title_full_unstemmed Porous 3D Scaffolds Enhance MSC Vitality and Reduce Osteoclast Activity
title_short Porous 3D Scaffolds Enhance MSC Vitality and Reduce Osteoclast Activity
title_sort porous 3d scaffolds enhance msc vitality and reduce osteoclast activity
topic 3D-printing
osteoclasts
mesenchymal stromal cells
tartrate-resistant acid phosphatase
mRNA expression
implant
url https://www.mdpi.com/1420-3049/26/20/6258
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AT christophbiehl porous3dscaffoldsenhancemscvitalityandreduceosteoclastactivity
AT klausliefeith porous3dscaffoldsenhancemscvitalityandreduceosteoclastactivity
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