Inflammatory responses and tissue reactions to wood-Based nanocellulose scaffolds.
Animals
Cell Proliferation
Cellulose
/ adverse effects
Cytokines
/ metabolism
Female
Gene Expression Regulation
Humans
Implants, Experimental
Inflammation
/ chemically induced
Materials Testing
/ methods
Nanostructures
/ adverse effects
Rats, Wistar
Tissue Scaffolds
/ adverse effects
U937 Cells
Wood
/ chemistry
Cellulose Nanofibrils
Cytokines
Degradation
Foreign body reaction
Inflammation
Macrophages
Journal
Materials science & engineering. C, Materials for biological applications
ISSN: 1873-0191
Titre abrégé: Mater Sci Eng C Mater Biol Appl
Pays: Netherlands
ID NLM: 101484109
Informations de publication
Date de publication:
Apr 2019
Apr 2019
Historique:
received:
10
08
2018
revised:
22
11
2018
accepted:
27
11
2018
entrez:
26
1
2019
pubmed:
27
1
2019
medline:
18
6
2019
Statut:
ppublish
Résumé
Two wood-derived cellulose nanofibril (CNF) porous scaffolds were prepared by TEMPO-oxidation and carboxymethylation. The effects of these scaffolds on the production of inflammatory cytokines by human macrophage-like cells (U937) was profiled in vitro after 1 and 3 days and in subcutaneous tissues of rats after 4 and 30 days, using PCR and Multiplex arrays. Tissue culture plates (TCP) and gelatin scaffolds served as controls in vitro and in vivo respectively. After 3 days in vitro, there was no significant difference between the effects of CNF scaffolds and TCP on the production of chemokines/growth factors and pro-inflammatory cytokines. At day 4 in vivo there was significantly higher gene expression of the anti-inflammatory IL-1Ra in the CNF scaffolds than the gelatin scaffold. Production of IL-1β, IL-6, MCP-1, MIP-1α CXCL-1 and M-CSF was significantly less than in the gelatin, demonstrating an early mild inflammatory response. At day 30, both CNF scaffolds significantly stimulated the production of the anti-inflammatory cytokine IL-10. Unlike gelatin, neither CNF scaffold had degraded 180 days post-implantation. The slow degradation of CNF scaffolds resulted in a foreign body reaction, with high production of IL-1β, IL-2, TNF-α, IFN-ϒ, MCP-1, MIP-1α, M-CSF, VEGF cytokines and expression of MMP-9 gene. The surface chemistry of the CNF scaffolds elicited a modest effect on cytokine production and did not shift the inflammatory profile in vitro or in vivo. The decisive role in development of the foreign body reaction was the slow degradation of the CNF scaffolds.
Identifiants
pubmed: 30678905
pii: S0928-4931(18)32413-5
doi: 10.1016/j.msec.2018.11.068
pii:
doi:
Substances chimiques
Cytokines
0
Cellulose
9004-34-6
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
208-221Informations de copyright
Copyright © 2018 Elsevier B.V. All rights reserved.