用于内源性间充质干细胞招募和原位牙周组织再生的工程化细胞外小泡

Cathy Tran, Ranya Elsayed PhD MBA
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引用次数: 0

摘要

目的免疫调节树突状细胞(regDCs)释放的外泌体已被用作一种有效的纳米递送系统,用于重新编程小鼠炎性骨缺损处的免疫反应。本研究旨在确定工程化SDF-1负载免疫调节DC衍生外泌体(SDF-1exo)在间充质干细胞招募和骨再生中的功效。用超声波将外泌体装入 SDF-1。对外显子货物进行了体外研究,包括SDF-1的抗蛋白水解性、间充质干细胞募集和成骨分化。然后在小鼠下颌骨缺损模型中测试了透明质酸水凝胶载体中 SDF-1exo 的治疗效果。测试共分五组(n=5):第 1 组(阴性对照)、第 2 组(单独载体)、第 3 组(不含外激素的载体)、第 4 组(含游离 SDF-1 的载体)和第 5 组(含 SDF-1-exo 的载体)。使用体内成像技术对 DiI 标记的 SDF-1-exo 进行生物分布。标本在术后2周和4周采集。结果SDF-1-exo能保护其载体不被赖氨酸鞘氨醇和DPP4蛋白水解,并促进间充质干细胞迁移和成骨。TEM显示了SDF-1在外膜腔和跨膜域的定位。阻断实验显示,可持续的SDF-1信号传导需要SDF-1exo与CXCR4受体之间的相互作用。在体内,SDF-1exo在缺损部位表现出很高的亲和力,并在愈合的头两周内维持SDF-1的表达,促进间充质干细胞的迁移。结论这项研究证明了 SDF-1exo 在促进骨再生方面的功效。
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Engineered Small Extra-Cellular Vesicles for Endogenous Mesenchymal Stem Cells Recruitment and in situ Periodontal Tissue Regeneration

OBJECTIVES

Exo released by immune-regulatory dendritic cells (regDCs) have been used as an effective nanodelivery system for the reprogramming of immune response at inflammatory bone defects in mice. This study aims to determine the efficacy of engineered SDF-1-loaded immune-regulatory DC-derived exosomes (SDF-1exo) in MSC recruitment and bone regeneration.

METHODS

Exo were purified from human and murine regDCs. Exo were loaded with SDF-1 using ultrasonication. In vitro studies of exo cargo including resistance of SDF-1 to proteolysis, MSC recruitment, and osteogenic differentiation were carried out. The therapeutic effect of SDF-1exo in hyaluronic acid-based hydrogel carrier was then tested in mandibular defects in a murine model. Five groups (n=5) were tested: group 1 (negative control), group 2 (carrier alone), group 3 (carrier with unloaded exo), group 4 (carrier with free SDF-1) and group 5 (carrier with SDF-1-exo). Biodistribution of DiI-prelabeled SDF-1-exo was performed using in-vivo imaging. Specimens were collected at 2- and 4-weeks post-operative. 3D volumetric micro-CT, histologic, qPCR, and IHC analyses were performed.

RESULTS

SDF-1exo protected its cargo against lysine gingipains and DPP4 proteolytic cleavage and promoted MSC migration, and osteogenesis. TEM revealed SDF-1 localization in the exo lumen and in the transmembrane domain. Blocking experiments revealed that sustainable SDF-1 signaling required interaction between SDF-1exo and CXCR4 receptor. In vivo, SDF-1exo showed a high affinity at the defect sites and sustained SDF-1 expression during the first 2 weeks of healing, promoting MSC migration. Significantly greater bone maturation in the SDF-1exo group was observed at 4 weeks.

CONCLUSIONS

This study demonstrated the efficacy of SDF-1exo delivery in promoting bone regeneration.

IMPLICATIONS

This study provides the basis for a novel natural nano-therapeutic strategy for periodontal tissue regeneration in humans.

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