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用于运动创伤韧带修复的聚氨酯支架引导间充质干细胞迁移研究

吕伯文¹,龚希丹2   

  1. 1. 郑州工业安全职业学院公共体育部 2. 河南理工大学体育学院
  • 收稿日期:2025-12-17 修回日期:2026-01-28 网络首发:2026-03-18 发布日期:2026-03-18
  • 通讯作者: 吕伯文 E-mail:13333839069@163.com
  • 基金资助:
    2024年河南省教师教育课程改革研究项目(批准号:2024-JSJYZD-005)资助

Study on the migration of mesenchymal stem cells guided by polyurethane scaffolds for repairing ligaments in sports injuries

LÜ Bowen1*, GONG Xidan2   

  1. 1. Department of Public Physical Education, Zhengzhou Industrial Safety Vocational College 2. School of Physical Education, Henan Polytechnic University
  • Received:2025-12-17 Revised:2026-01-28 Online First:2026-03-18 Published:2026-03-18
  • Contact: Bowen Lv E-mail:13333839069@163.com
  • Supported by:
    Supported by the Research Project on Teacher Education Curriculum Reform in Henan Province in 2024 (No. 2024-JSJYZD-005)

摘要: 本研究开发了一种基于马兰戈尼效应制备的具有定向纳米凹槽(宽度2-3 μm,粗糙度Ra=185±32 nm)的聚氨酯支架。通过扫描电镜、原子力显微镜、偏振光显微镜表征其形貌与晶体结构;采用单轴拉伸和循环疲劳测试评估其静态与动态力学性能,显示弹性模量与天然韧带匹配且抗疲劳性优异;溶血试验和Live/Dead染色证实其生物相容性良好(溶血率<5%,细胞存活率高)。分离培养大鼠骨髓间充质干细胞(MSC)并接种于聚氨酯材料表面,分为静态平滑表面组(SS)、静态纳米凹槽组(SN)及动态拉伸纳米凹槽组(DN),其中DN组施加5%应变的动态拉伸刺激。通过划痕实验、EdU染色、细胞骨架/黏着斑染色分析细胞迁移、增殖与粘附行为;利用qPCR与Western Blot检测YAP、整合素通路相关分子表达。实验结果显示:SN组在静态下可引导MSC定向排列与迁移;DN组在纳米拓扑与动态拉伸协同作用下,细胞迁移速度、增殖活性、骨架定向性及黏着斑成熟度均显著增强。分子机制表明,协同刺激协同性上调YAP、CTGF、CYR61及整合素β1的基因表达,并促进YAP蛋白核转位。综上,该支架成功实现通过激活YAP信号通路驱动MSC迁移与增殖,兼具生物安全性、力学匹配性与动态响应性。

关键词: 运动损伤, 聚氨酯支架, 动态拉伸, 间充质干细胞, Yes相关蛋白信号通路

Abstract: This study developed a polyurethane scaffold featuring aligned nanogrooves (width: 2-3 μm, roughness Ra = 185 ± 32 nm) fabricated based on the Marangoni effect. Its morphology and crystalline structure were characterized by scanning electron microscopy (SEM), atomic force microscopy (AFM), and polarized light microscopy. Uniaxial tensile and cyclic fatigue tests evaluated its static and dynamic mechanical properties, demonstrating an elastic modulus matching that of natural ligaments and excellent fatigue resistance. Hemolysis assays and Live/Dead staining confirmed its good biocompatibility (hemolysis rate < 5%, high cell viability). Rat bone marrow-derived mesenchymal stem cells (MSCs) were isolated, cultured, and seeded onto the polyurethane scaffold surfaces. The cells were divided into three groups: static smooth surface (SS), static nanogrooved surface (SN), and dynamic stretched nanogrooved surface (DN), with the DN group subjected to dynamic tensile stimulation at 5% strain. Cell migration, proliferation, and adhesion behaviors were analyzed via scratch wound assay, EdU staining, and cytoskeleton/focal adhesion staining. The expression of YAP and integrin pathway-related molecules was detected using qPCR and Western Blot. Experimental results showed that the SN group could guide the alignment and migration of MSCs under static conditions. The DN group, under the synergistic effect of nanotopography and dynamic stretching, exhibited significantly enhanced cell migration speed, proliferation activity, cytoskeletal alignment, and focal adhesion maturation. Molecular mechanistic studies indicated that the combined stimulation synergistically upregulated the gene expression of YAP, CTGF, CYR61, and integrin β1, and promoted YAP protein nuclear translocation. In conclusion, this scaffold successfully drives MSC migration and proliferation by activating the YAP signaling pathway, while possessing biosafety, mechanical compatibility, and dynamic responsiveness.

Key words: Polyurethane scaffold, Nanogroove, Mesenchymal stem cell, Dynamic stretching, Yes-associated protein signaling

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