Oxidized Xanthan Gum Cross-Linked N-O Carboxymethyl Chitosan Hydrogel Promotes Spheroid Formation of Murine Fibroblast by Increasing Cell-Cell Interaction and Integrin αv Expression.

IF 5.5 2区 医学 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Biomaterials Science & Engineering Pub Date : 2025-04-14 Epub Date: 2025-03-24 DOI:10.1021/acsbiomaterials.5c00125
Thai Huynh Anh, Thao Thi-Phuong Nguyen, Hang Phuong Huynh, Thu-La Ngoc Minh, Hai-Nguyen Huu, Hoan Ngoc Doan, Binh Thanh Vu, Vo Minh Quan, Thi-Hiep Nguyen, Han Thi Ngoc To
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Abstract

Naturally derived Schiff-based hydrogels are widely fabricated for tissue engineering applications. However, limited studies have explored how the physicochemical and functional groups on polymer chains affect cell behavior in three dimensions. To address this limitation, we fabricated cytocompatible N-O carboxymethyl chitosan (NOCC) cross-linked with oxidized xanthan gum (OXG), incorporating various aldehyde (-CHO) contents (NO1, NO2, and NO3) while maintaining a constant concentration of NOCC, resulting in hydrogels with diverse viscoelastic and aldehyde content properties. The results demonstrated significant differences in storage modulus (G') and loss modulus (G″), attributed to cross-linking density through imine bonds (-C═N-). These differences influenced murine fibroblast aggregation, spheroid formation, and cell migration, proliferation, and viability over time. Both NO1 and NO2 exhibited good cell viability, with slight differences in spheroid morphology compared to those of NO3 and Matrigel samples. To further explore cell behaviors, integrin αV (CD51) expression was assessed using fluorescence-activated cell sorting (FACS) and immunofluorescence. The results aligned with prior observations, with the quantitative analysis of integrin αV expression, normalized to 4',6-diamidino-2-phenylindole (DAPI) fluorescence, revealing a notable 2.1-fold increase in fluorescence intensity for the NO2 hydrogel in comparison to NO1 (p < 0.0001). These findings indicate that the hydrogel composed of 2% (w/v) NOCC cross-linked with 2% (w/v) OXG in a 1:1 (v/v) ratio represents the optimal condition for promoting murine fibroblast growth and spheroid formation. These results provide a robust foundation for future research aimed at modulating cell behavior through precise adjustments of scaffold properties, thereby advancing the potential for translational applications from laboratory research to clinical settings.

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氧化黄原胶交联N-O羧甲基壳聚糖水凝胶通过增加细胞间相互作用和整合素αv表达促进小鼠成纤维细胞球形形成。
天然衍生的希夫基水凝胶广泛用于组织工程应用。然而,有限的研究探索了聚合物链上的物理化学和官能团如何在三维上影响细胞行为。为了解决这一限制,我们制备了细胞相容性N-O羧甲基壳聚糖(NOCC),并与氧化黄原胶(OXG)交联,加入不同的醛(-CHO)含量(NO1, NO2和NO3),同时保持恒定的NOCC浓度,从而得到具有不同粘弹性和醛含量性质的水凝胶。结果显示存储模量(G′)和损耗模量(G″)有显著差异,这是由于通过亚胺键(c = N-)交联的密度。随着时间的推移,这些差异影响了小鼠成纤维细胞聚集、球状体形成和细胞迁移、增殖和活力。NO1和NO2均表现出良好的细胞活力,与NO3和Matrigel样品相比,其球状形态略有差异。为了进一步了解细胞行为,采用荧光活化细胞分选(FACS)和免疫荧光技术评估整合素αV (CD51)的表达。结果与之前的观察结果一致,通过定量分析整合素αV的表达,归一化为4',6-二氨基-2-苯基吲哚(DAPI)荧光,NO2水凝胶的荧光强度比NO1提高了2.1倍(p < 0.0001)。上述结果表明,2% (w/v) NOCC与2% (w/v) OXG以1:1 (v/v)比例交联的水凝胶是促进小鼠成纤维细胞生长和球状体形成的最佳条件。这些结果为未来的研究提供了坚实的基础,旨在通过精确调节支架特性来调节细胞行为,从而推进从实验室研究到临床环境的转化应用潜力。
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来源期刊
ACS Biomaterials Science & Engineering
ACS Biomaterials Science & Engineering Materials Science-Biomaterials
CiteScore
10.30
自引率
3.40%
发文量
413
期刊介绍: ACS Biomaterials Science & Engineering is the leading journal in the field of biomaterials, serving as an international forum for publishing cutting-edge research and innovative ideas on a broad range of topics: Applications and Health – implantable tissues and devices, prosthesis, health risks, toxicology Bio-interactions and Bio-compatibility – material-biology interactions, chemical/morphological/structural communication, mechanobiology, signaling and biological responses, immuno-engineering, calcification, coatings, corrosion and degradation of biomaterials and devices, biophysical regulation of cell functions Characterization, Synthesis, and Modification – new biomaterials, bioinspired and biomimetic approaches to biomaterials, exploiting structural hierarchy and architectural control, combinatorial strategies for biomaterials discovery, genetic biomaterials design, synthetic biology, new composite systems, bionics, polymer synthesis Controlled Release and Delivery Systems – biomaterial-based drug and gene delivery, bio-responsive delivery of regulatory molecules, pharmaceutical engineering Healthcare Advances – clinical translation, regulatory issues, patient safety, emerging trends Imaging and Diagnostics – imaging agents and probes, theranostics, biosensors, monitoring Manufacturing and Technology – 3D printing, inks, organ-on-a-chip, bioreactor/perfusion systems, microdevices, BioMEMS, optics and electronics interfaces with biomaterials, systems integration Modeling and Informatics Tools – scaling methods to guide biomaterial design, predictive algorithms for structure-function, biomechanics, integrating bioinformatics with biomaterials discovery, metabolomics in the context of biomaterials Tissue Engineering and Regenerative Medicine – basic and applied studies, cell therapies, scaffolds, vascularization, bioartificial organs, transplantation and functionality, cellular agriculture
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