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通过包封在多样化丝素基可注射水凝胶中的免疫调节细胞外囊泡增强组织再生。

Enhanced Tissue Regeneration Through Immunomodulatory Extracellular Vesicles Encapsulated in Diversified Silk-Based Injectable Hydrogels.

机构信息

Department of Orthodontics, Department of Macromolecular Science, Multidisciplinary Consultant Center, Shanghai Stomatological Hospital & School of Stomatology, Fudan University, Shanghai, 200001, China.

Shanghai Key Laboratory of Craniomaxillofacial Development and Diseases, Fudan University, Shanghai, 200001, China.

出版信息

Adv Healthc Mater. 2024 Nov;13(28):e2401460. doi: 10.1002/adhm.202401460. Epub 2024 Jul 16.

DOI:10.1002/adhm.202401460
PMID:39011805
Abstract

Mesenchymal stem cells (MSCs) immunologically trained using lipopolysaccharide (LPS) display enhanced immunomodulatory capabilities. Extracellular vesicles (EVs) derived from MSCs are widely used in regenerative medicine owing to their bioactive properties without the drawbacks of cell therapy. However, it remains unclear whether EVs derived from LPS-stimulated (trained) MSCs (L-EVs) inherit the enhanced reparative potential from their parent cells. Thus, this study first aims to explore the effect of immunological training on the bioactivity of L-EVs. LPS-trained bone marrow-derived MSCs (BMSCs) secrete more EVs, and these EVs significantly promote M2 macrophage polarization. Subsequently, hydrogel systems based on thixotropic injectable silk fibroin are prepared for in vivo EV delivery. These hydrogels have controllable gelation time and exhibit outstanding reparative effects on rat skin wounds and alveolar bone defects. Finally, it is revealed that L-EVs promote M2 macrophage polarization by inhibiting the nuclear translocation of PKM2. Overall, this study shows that the immunological training of BMSCs effectively improves the therapeutic effects of their EVs and provides a convenient and diversified EV delivery strategy using an injectable silk fibroin hydrogel. This strategy has broad clinical application prospects for tissue regeneration.

摘要

间充质干细胞(MSCs)经脂多糖(LPS)免疫驯化后显示出增强的免疫调节能力。由于具有生物活性而没有细胞治疗的缺点,源自 MSCs 的细胞外囊泡(EVs)广泛用于再生医学。然而,尚不清楚源自 LPS 刺激(驯化)的 MSCs(L-EVs)的 EV 是否继承了其亲本细胞的增强修复潜能。因此,本研究首先旨在探索免疫驯化对 L-EVs 生物活性的影响。LPS 驯化的骨髓来源的 MSCs(BMSCs)分泌更多的 EVs,这些 EVs 显著促进 M2 巨噬细胞极化。随后,基于触变可注射丝素蛋白制备水凝胶系统用于体内 EV 递送。这些水凝胶具有可控的凝胶时间,并对大鼠皮肤伤口和牙槽骨缺损具有出色的修复作用。最后,结果表明 L-EVs 通过抑制 PKM2 的核易位来促进 M2 巨噬细胞极化。总体而言,本研究表明 BMSCs 的免疫驯化可有效提高其 EV 的治疗效果,并提供了一种使用可注射丝素蛋白水凝胶的方便多样的 EV 递送策略。该策略为组织再生提供了广阔的临床应用前景。

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