Electrohydrodynamic‐Printed Dual‐Triphase Microfibrous Scaffolds Reshaping the Lipidomic Profile for Enthesis Healing in a Rat Rotator Cuff Repair Model

热情 肩袖 纤维软骨 生物医学工程 细胞生物学 下调和上调 骨整合 材料科学 肌腱 医学 化学 外科 生物 植入 病理 骨关节炎 生物化学 替代医学 基因 关节软骨
作者
Lang Bai,Ayiguli Kasimu,Shuai Wang,Zhennan Qiu,Meiguang Xu,Xiaoli Qu,B. Chen,Qiaonan Liu,Yixiang Ai,Meng Li,Jintao Xiu,Kai Liu,Nuanyang Wen,Jiankang He,Jing Zhang,Z. Yin
出处
期刊:Small [Wiley]
卷期号:21 (2): e2406069-e2406069 被引量:4
标识
DOI:10.1002/smll.202406069
摘要

Abstract Rotator cuff injuries often result in chronic pain and functional limitations due to retears and scar formation at the enthesis. This study assess the efficacy of electrohydrodynamic‐printed microfibrous dual‐triphase scaffolds (DTSs), designed to optimize enthesis repair. These scaffolds, composed of polycaprolactone enhanced with nanohydroxyapatite, nano‐magnesium‐oxide, and kartogenin demonstrate significant biological advantages. In vitro, the scaffolds support over 95% stem cell viability and promote enhanced expression of critical markers such as tenomodulin (TNMD), sex‐determining region Y‐Box transcription factor 9 (SOX‐9), and runt‐related transcription factor 2 (RUNX‐2). Enhanced expressions of tendon markers tenomodulin and scleraxis (SCX) are noted, alongside significant upregulation of chondrocyte and osteoblast markers. In vivo, these scaffolds significantly improve the biomechanical properties of the repaired enthesis, with a maximum failure load of 27.0 ± 4.2 N and ultimate stress of 5.5 ± 1.0 MPa at 6 weeks postimplantation. Lipidomic analysis indicates substantial regulation of phospholipids such as phosphatidylcholine and phosphatidylserine, highlighting the scaffold's capacity to modulate biochemical pathways critical for tissue repair and regeneration. This study underscores the potential of DTS to improve clinical outcomes in rotator cuff injury treatment by enhancing cellular differentiation, biomechanical properties, and biochemical environment, setting a foundation for personalized treatment strategies in tendon–bone repair.
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