Silk based scaffolds with immunomodulatory capacity: anti-inflammatory effects of nicotinic acid.
Animals
Anti-Inflammatory Agents
/ chemistry
Arthropod Proteins
/ chemistry
Biocompatible Materials
/ chemistry
Bombyx
/ metabolism
Cell Line
Cell Proliferation
/ drug effects
Cytokines
/ genetics
Delayed-Action Preparations
Down-Regulation
Humans
Macrophages
/ cytology
Materials Testing
Niacin
/ chemistry
Porosity
Silk
/ chemistry
Tissue Engineering
Tissue Scaffolds
/ chemistry
Journal
Biomaterials science
ISSN: 2047-4849
Titre abrégé: Biomater Sci
Pays: England
ID NLM: 101593571
Informations de publication
Date de publication:
17 Dec 2019
17 Dec 2019
Historique:
pubmed:
31
10
2019
medline:
15
4
2020
entrez:
31
10
2019
Statut:
ppublish
Résumé
Implantation of temporary and permanent biomaterials in the body leads to a foreign body reaction (FBR), which may adversely affect tissue repair processes and functional integration of the biomaterial. However, modulation of the inflammatory response towards biomaterials can potentially enable a favorable healing response associated with functional tissue formation and tissue regeneration. In this work, incorporation of nicotinic acid in 3D silk scaffolds is explored as an immunomodulatory strategy for implantable biomaterials. Silk scaffolds were fabricated from dissolved Bombyx mori silk fibers by freeze-drying, resulting in silk scaffolds with high porosity (>94%), well-connected macropores, a high swelling degree (>550%) and resistance to in vitro degradation. Furthermore, drug-loaded scaffolds displayed a sustained drug release and excellent cytocompatibility could be observed with osteoblast-like MG63 cells. Cultivating M1-like macrophages on the scaffolds revealed that scaffolds loaded with nicotinic acid suppress gene expression of pro-inflammatory markers TNF-α, CXCL10 and CD197 as well as secretion of TNF-α in a concentration dependant manner. Hence, this study provides insights into the possible application of nicotinic acid in tissue engineering to control inflammatory responses towards biomaterials and potentially help minimizing FBR.
Substances chimiques
Anti-Inflammatory Agents
0
Arthropod Proteins
0
Biocompatible Materials
0
Cytokines
0
Delayed-Action Preparations
0
Silk
0
Niacin
2679MF687A
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
148-162Commentaires et corrections
Type : ErratumIn