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Int J Biol Macromol ; 270(Pt 2): 132416, 2024 Jun.
Article in English | MEDLINE | ID: mdl-38754653

ABSTRACT

Inflammation-related bone defects often lead to poor osteogenesis. Therefore, it is crucial to reduce the inflammation response and promote the osteogenic differentiation of stem/progenitor cells to revitalize bone physiology. Here, a kind of hybrid nano-hydroxyapatite was prepared using the confined phosphate ion release method with the participation of fucoidan, a marine-sourced polysaccharide with anti-inflammation property. The physicochemical analyses confirmed that the fucoidan hybrid nano-hydroxyapatite (FC/n-HA) showed fine needle-like architectures. With a higher amount of fucoidan, the crystal size and crystallinity of the FC/n-HA reduced while the liquid dispersibility was improved. Cell experiences showed that FC/n-HA had an optimal cytocompatibility at concentration of 50 µg/mL. Moreover, the lipopolysaccharide-induced cellular inflammatory model with PDLSCs was established and used to evaluate the anti-inflammatory and osteogenic properties. For the 1%FC/n-HA group, the expression levels of TNF-α and IL-1ß were significantly reduced at 24 h, while the expression of alkaline phosphatase of PDLSCs was significantly promoted at days 3 and 7, and calcium precipitates was enhanced at 21 days. In this study, the FC/n-HA particles showed effective anti-inflammatory properties and facilitated osteogenic differentiation of PDLSCs, indicating which has potential application in treating bone defects associated with inflammation, such as periodontitis.


Subject(s)
Cell Differentiation , Durapatite , Nanoparticles , Osteogenesis , Periodontal Ligament , Polysaccharides , Stem Cells , Humans , Osteogenesis/drug effects , Polysaccharides/pharmacology , Polysaccharides/chemistry , Durapatite/chemistry , Durapatite/pharmacology , Cell Differentiation/drug effects , Stem Cells/drug effects , Stem Cells/cytology , Stem Cells/metabolism , Nanoparticles/chemistry , Periodontal Ligament/cytology , Periodontal Ligament/drug effects , Inflammation/drug therapy , Inflammation/pathology , Cells, Cultured
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