Department of Agro-Environmental Sciences, Graduate School of Bioresource and Bioenvironmental Sciences, Kyushu University, Fukuoka 819-0395, Japan.
Yokogawa Bio Frontier Inc., Musashino, Tokyo 180-8750, Japan.
Carbohydr Polym. 2024 Nov 1;343:122479. doi: 10.1016/j.carbpol.2024.122479. Epub 2024 Jul 10.
Stem cell culture often requires various animal-derived components such as serum and collagen. This limits its practical use. Therefore, xeno-free (xenogeneic component-free) culture systems are receiving increased attention. Herein, we propose xeno-free, plant-derived cellulose nanofibers (CNFs) with different surface chemistry: 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO)-oxidized CNFs (TOCNFs) with carboxy groups and surface-sulfated CNFs (S-CNFs) for the proliferation of human mesenchymal stem cells (hMSCs) under various serum conditions. We cultured bone marrow-derived hMSCs on CNF scaffolds with various fiber lengths and functional group contents. Original CNFs were bioinert materials that did not contribute to cell adhesion. In contrast, the surface-modified CNFs facilitated the proliferation of immortalized hMSCs under normal and low-serum conditions. The TOCNFs (COONa: 1.47 mmol g; length: 0.53 μm), the S-CNFs (OSONa: 0.64 mmol g; 0.61 μm), and a combination of the two (1:1 by weight) enabled immortalized hMSCs to maintain their multipotency, even under serum-free conditions. Primary cultured hMSCs proliferated well on the TOCNF/S-CNF scaffolds in a completely serum-free medium, comparable to animal-derived type I collagen, although few hMSCs adhered to the standard polystyrene substrate. Our strategy of using surface-modified CNFs will inform the development of xeno-free culture systems to avoid the use of animal-derived materials for both cell culture media and scaffolds.
干细胞培养通常需要各种动物源性成分,如血清和胶原蛋白。这限制了其实际应用。因此,无动物成分(无异种成分)的培养系统越来越受到关注。在这里,我们提出了具有不同表面化学性质的无动物成分、植物衍生的纤维素纳米纤维(CNFs):带有羧基的 2,2,6,6-四甲基哌啶-1-氧自由基(TEMPO)氧化的 CNFs(TOCNFs)和表面磺化的 CNFs(S-CNFs),用于在各种血清条件下促进人骨髓间充质干细胞(hMSCs)的增殖。我们在具有不同纤维长度和官能团含量的 CNF 支架上培养骨髓来源的 hMSCs。原始 CNF 是生物惰性材料,不会促进细胞黏附。相比之下,表面改性的 CNF 促进了永生化 hMSCs 在正常和低血清条件下的增殖。TOCNFs(COONa:1.47 mmol g;长度:0.53 μm)、S-CNFs(OSONa:0.64 mmol g;0.61 μm)和两者的混合物(按重量 1:1)使永生化 hMSCs 即使在无血清条件下也能保持多能性。原代培养的 hMSCs 在完全无血清培养基中在 TOCNF/S-CNF 支架上增殖良好,与动物来源的 I 型胶原相当,尽管很少有 hMSCs 黏附在标准聚苯乙烯基质上。我们使用表面改性 CNF 的策略将为无动物成分培养系统的开发提供信息,以避免在细胞培养基和支架中使用动物源性材料。