Maintenance of Ligament Homeostasis of Spheroid-Colonized Embroidered and Functionalized Scaffolds after 3D Stretch.


Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
30 Jul 2021
Historique:
received: 18 06 2021
revised: 18 07 2021
accepted: 23 07 2021
entrez: 7 8 2021
pubmed: 8 8 2021
medline: 9 9 2021
Statut: epublish

Résumé

Anterior cruciate ligament (ACL) ruptures are usually treated with autograft implantation to prevent knee instability. Tissue engineered ACL reconstruction is becoming promising to circumvent autograft limitations. The aim was to evaluate the influence of cyclic stretch on lapine (L) ACL fibroblasts on embroidered scaffolds with respect to adhesion, DNA and sulphated glycosaminoglycan (sGAG) contents, gene expression of ligament-associated extracellular matrix genes, such as type I collagen, decorin, tenascin C, tenomodulin, gap junctional connexin 43 and the transcription factor Mohawk. Control scaffolds and those functionalized by gas phase fluorination and cross-linked collagen foam were either pre-cultured with a suspension or with spheroids of LACL cells before being subjected to cyclic stretch (4%, 0.11 Hz, 3 days). Stretch increased significantly the scaffold area colonized with cells but impaired sGAGs and decorin gene expression (functionalized scaffolds seeded with cell suspension). Stretching increased tenascin C, connexin 43 and Mohawk but decreased decorin gene expression (control scaffolds seeded with cell suspension). Pre-cultivation of functionalized scaffolds with spheroids might be the more suitable method for maintaining ligamentogenesis in 3D scaffolds compared to using a cell suspension due to a significantly higher sGAG content in response to stretching and type I collagen gene expression in functionalized scaffolds.

Identifiants

pubmed: 34360970
pii: ijms22158204
doi: 10.3390/ijms22158204
pmc: PMC8348491
pii:
doi:

Substances chimiques

Connexins 0
Decorin 0
Extracellular Matrix Proteins 0
Homeodomain Proteins 0
Polyesters 0
lactide-caprolactone copolymer 70524-20-8

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Deutsche Forschungsgemeinschaft
ID : ME 3734/2-1, ME 3734/5-1, SCHU 1979/9-1, SCHU 1979/14-1, BR 1886/6-1, BR 5604/1-1, HE 4466/22-1,

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Auteurs

Clemens Gögele (C)

Institute of Anatomy and Cell Biology, Paracelsus Medical University, Nuremberg and Salzburg, Prof. Ernst Nathan Str. 1, 90419 Nuremberg, Germany.
Department of Biosciences, Paris Lodron University of Salzburg, Hellbrunnerstr. 34, 5020 Salzburg, Austria.

Jens Konrad (J)

Institute of Biological Information Processing: IBI-2, Forschungszentrum Jülich, 52425 Jülich, Germany.

Judith Hahn (J)

Workgroup BioEngineering, Department Materials Engineering, Institute of Polymers Materials, Leibniz-Institut für Polymerforschung Dresden e.V. (IPF), Dresden, Hohe Straße 6, 01069 Dresden, Germany.

Annette Breier (A)

Workgroup BioEngineering, Department Materials Engineering, Institute of Polymers Materials, Leibniz-Institut für Polymerforschung Dresden e.V. (IPF), Dresden, Hohe Straße 6, 01069 Dresden, Germany.

Michaela Schröpfer (M)

FILK Freiberg Institute GmbH, Meißner Ring 1-5, 09599 Freiberg, Germany.

Michael Meyer (M)

FILK Freiberg Institute GmbH, Meißner Ring 1-5, 09599 Freiberg, Germany.

Rudolf Merkel (R)

Institute of Biological Information Processing: IBI-2, Forschungszentrum Jülich, 52425 Jülich, Germany.

Bernd Hoffmann (B)

Institute of Biological Information Processing: IBI-2, Forschungszentrum Jülich, 52425 Jülich, Germany.

Gundula Schulze-Tanzil (G)

Institute of Anatomy and Cell Biology, Paracelsus Medical University, Nuremberg and Salzburg, Prof. Ernst Nathan Str. 1, 90419 Nuremberg, Germany.

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Classifications MeSH