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三维胶原基质中间充质干细胞的免疫调节特性

Immunomodulatory properties of mesenchymal stem cells within three-dimensional collagen matrices.

作者信息

Yustisia Yenny, Kato Koichi

机构信息

Department of Biomaterials, Graduate School of Biomedical and Health Sciences, Hiroshima University, 1-2-3, Kasumi, Minami-ku, Hiroshima, 734-8553, Japan.

Department of Oral Biology, Faculty of Dentistry, University of Jember, Kalimantan 37, Jember, Indonesia.

出版信息

In Vitro Cell Dev Biol Anim. 2025 Sep 15. doi: 10.1007/s11626-025-01109-z.

Abstract

Mesenchymal stem cells (MSCs) hold promise for treating inflammatory and immune-related diseases; however, their clinical application is limited by poor survival and function post-transplantation. Collagen hydrogels may support MSC viability and function by mimicking the extracellular matrix. This study aimed to evaluate how cell density and collagen concentration within three-dimensional (3D) collagen matrices affect the immunomodulatory behavior of MSCs under inflammatory conditions. MSCs were embedded in collagen hydrogels of varying stiffness and seeded at different densities. Constructs were stimulated with proinflammatory cytokines (tumor necrosis factor-α and interferon-γ), and changes in Gene expression, hydrogel contraction, and cell viability were analyzed. Lower collagen concentrations and higher seeding densities enhanced MSC immunomodulatory Gene expression and matrix contraction. High cell density increased contraction but reduced cell viability in softer gels. Mechanical properties of the matrix, such as stiffness and viscoelasticity, influenced cell behavior via mechanotransduction pathways. Both physical and biological cues within 3D collagen hydrogels significantly regulated MSC immunomodulatory responses. Optimizing collagen concentration and seeding density may improve the therapeutic potential of MSC-based treatments.

摘要

间充质干细胞(MSCs)有望用于治疗炎症和免疫相关疾病;然而,其临床应用受到移植后存活率低和功能受限的限制。胶原蛋白水凝胶可以通过模拟细胞外基质来支持间充质干细胞的活力和功能。本研究旨在评估三维(3D)胶原蛋白基质中的细胞密度和胶原蛋白浓度如何影响炎症条件下间充质干细胞的免疫调节行为。将间充质干细胞嵌入不同硬度的胶原蛋白水凝胶中,并以不同密度接种。用促炎细胞因子(肿瘤坏死因子-α和干扰素-γ)刺激构建体,并分析基因表达、水凝胶收缩和细胞活力的变化。较低的胶原蛋白浓度和较高的接种密度增强了间充质干细胞免疫调节基因的表达和基质收缩。高细胞密度增加了收缩,但降低了较软凝胶中的细胞活力。基质的机械性能,如硬度和粘弹性,通过机械转导途径影响细胞行为。3D胶原蛋白水凝胶中的物理和生物学线索均显著调节间充质干细胞的免疫调节反应。优化胶原蛋白浓度和接种密度可能会提高基于间充质干细胞治疗的治疗潜力。

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