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Carbohydr Polym ; 343: 122479, 2024 Nov 01.
Artigo em Inglês | MEDLINE | ID: mdl-39174138

RESUMO

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-1; length: 0.53 µm), the S-CNFs (OSO3Na: 0.64 mmol g-1; 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.


Assuntos
Proliferação de Células , Celulose , Células-Tronco Mesenquimais , Nanofibras , Alicerces Teciduais , Humanos , Células-Tronco Mesenquimais/citologia , Células-Tronco Mesenquimais/efeitos dos fármacos , Nanofibras/química , Celulose/química , Alicerces Teciduais/química , Proliferação de Células/efeitos dos fármacos , Células Cultivadas , Propriedades de Superfície , Adesão Celular/efeitos dos fármacos , Óxidos N-Cíclicos/química , Técnicas de Cultura de Células/métodos , Diferenciação Celular/efeitos dos fármacos
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