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载 JAK/STAT 抑制剂纳米囊泡的双芒微针治疗肌腱病

Dual-Barb Microneedle with JAK/STAT Inhibitor-Loaded Nanovesicles Encapsulation for Tendinopathy.

机构信息

Department of Orthopaedics, Affiliated Hospital of Nantong University, Nantong, 226001, China.

Department of Orthopaedics, The Second Hospital of Dalian Medical University, Dalian, 116023, China.

出版信息

Adv Healthc Mater. 2024 Nov;13(28):e2401512. doi: 10.1002/adhm.202401512. Epub 2024 Jul 19.

Abstract

Tendon stem/progenitor cells (TSPCs) are crucial for tendon repair, regeneration, and homeostasis. Dysfunction of TSPCs, due to aberrant activation of the Janus kinase/signal transducer and activator of transcription (JAK/STAT) signaling pathway, contributes to tendinopathy. Unfortunately, the effectiveness of conventional subcutaneous injection targeting at suppressing JAK/STAT signaling pathway is limited due to the passive diffusion of drugs away from the injury site. Herein, a novel poly-gamma-glutamic acid (γ-PGA) dual-barb microneedle (MN) path loaded with TSPCs-derived nanovesicles (NVs) containing JAK/STAT inhibitor WP1066 (MN-WP1066-NVs) for tendinopathy treatment is designed. The dual-barb design of the MN ensures firm adhesion to the skin, allowing for sustained and prolonged release of WP1066-NVs, facilitating enhanced TSPCs self-renewal, migration, and stemness in tendinopathy. In vitro and in vivo experiments demonstrate that the degradation of γ-PGA patch tips facilitates the gradual release of WP1066-NVs at the lesion site. This release alleviates inflammation, suppresses extracellular matrix degradation, and restores normal tendon histological structure by inhibiting the JAK/STAT pathway. These findings suggest that the multifunctional dual-barb MN patch offers a novel and effective therapeutic strategy for tendinopathy treatment.

摘要

肌腱干/祖细胞(TSPCs)对于肌腱修复、再生和稳态至关重要。由于 Janus 激酶/信号转导和转录激活因子(JAK/STAT)信号通路的异常激活,TSPCs 的功能障碍导致了腱病。不幸的是,由于药物从损伤部位的被动扩散,传统的针对抑制 JAK/STAT 信号通路的皮下注射效果有限。在此,设计了一种新型聚-γ-谷氨酸(γ-PGA)双倒刺微针(MN)贴片,负载含有 JAK/STAT 抑制剂 WP1066 的 TSPCs 衍生纳米囊泡(MN-WP1066-NVs),用于腱病治疗。MN 的双倒刺设计确保了与皮肤的牢固附着,允许 WP1066-NVs 的持续和延长释放,促进腱病中 TSPCs 的自我更新、迁移和干性。体内外实验表明,γ-PGA 贴片尖端的降解有助于 WP1066-NVs 在病变部位的逐渐释放。这种释放通过抑制 JAK/STAT 通路缓解炎症、抑制细胞外基质降解并恢复正常的肌腱组织学结构。这些发现表明,多功能双倒刺 MN 贴片为腱病治疗提供了一种新颖而有效的治疗策略。

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