Center of Translational Oral Research (TOR), Department of Clinical Dentistry, University of Bergen, Bergen 5009, Norway.
Department of Biotechnology and Food Science, Norwegian University of Science and Technology, Trondheim 7491, Norway.
ACS Appl Bio Mater. 2023 Mar 20;6(3):987-998. doi: 10.1021/acsabm.2c00794. Epub 2023 Feb 10.
Cellulose nanofibrils (CNFs) are multiscale hydrophilic biocompatible polysaccharide materials derived from wood and plants. TEMPO-mediated oxidation of CNFs (TO-CNF) turns some of the primary hydroxyl groups to carboxylate and aldehyde groups. Unlike carboxylic functional groups, there is little or no information about the biological role of the aldehyde groups on the surface of wood-based CNFs. In this work, we replaced the aldehyde groups in the TO-CNF samples with carboxyl groups by another oxidation treatment (TO-O-CNF) or with primary alcohols with terminal hydroxyl groups by a reduction reaction (TO-R-CNF). Rat mesenchymal stem/stromal cells (MSCs) derived from bone marrow were seeded on polystyrene tissue culture plates (TCP) coated with CNFs with and without aldehyde groups. TCP and TCP coated with bacterial nanocellulose (BNC) were used as control groups. Protein adsorption measurements demonstrated that more proteins were adsorbed from cell culture media on all CNF surfaces compared to BNC. Live/dead and lactate dehydrogenase assays confirmed that all nanocellulose biomaterials supported excellent cell viability. Interestingly, TO-R-CNF samples, which have no aldehyde groups, showed better cell spreading than BNC and comparable results to TCP. Unlike TO-O-CNF surfaces, which have no aldehyde groups either, TO-R-CNF stimulated cells, in osteogenic medium, to have higher alkaline phosphatase activity and to form more biomineralization than TCP and TO-CNF groups. These findings indicate that the presence of aldehyde groups (280 ± 14 μmol/g) on the surface of TEMPO-oxidized CNFs might have little or no effect on attachment, proliferation, and osteogenic differentiation of MSCs.
纤维素纳米纤维(CNFs)是一种多尺度亲水性生物相容性多糖材料,来源于木材和植物。TEMPO 介导的 CNFs 氧化(TO-CNF)将一些伯羟基转化为羧基和醛基。与羧酸官能团不同,关于木质素基 CNFs 表面醛基的生物学作用知之甚少。在这项工作中,我们通过另一种氧化处理(TO-O-CNF)将 TO-CNF 样品中的醛基替换为羧基,或者通过还原反应(TO-R-CNF)将其替换为带末端羟基的伯醇。从骨髓中分离的大鼠间充质干细胞/基质细胞(MSCs)接种在涂有 CNF 的聚苯乙烯组织培养板(TCP)上,这些 CNF 带有或不带有醛基。TCP 和涂有细菌纳米纤维素(BNC)的 TCP 用作对照组。蛋白质吸附测量表明,与 BNC 相比,所有 CNF 表面从细胞培养基中吸附了更多的蛋白质。活/死和乳酸脱氢酶测定证实,所有纳米纤维素生物材料都具有出色的细胞活力。有趣的是,没有醛基的 TO-R-CNF 样品比 BNC 和 TCP 表现出更好的细胞铺展。与没有醛基的 TO-O-CNF 表面不同,TO-R-CNF 刺激细胞在成骨培养基中具有更高的碱性磷酸酶活性并形成比 TCP 和 TO-CNF 组更多的生物矿化。这些发现表明,TEMPO 氧化 CNFs 表面上存在的醛基(280 ± 14 μmol/g)可能对 MSCs 的附着、增殖和成骨分化几乎没有影响。