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工程化衍生的外膜囊泡靶向骨微环境以改善骨质疏松症。

Engineered -Derived Outer Membrane Vesicles Targeting Bone Microenvironment to Improve Osteoporosis.

作者信息

Lin Sanfu, Chen Chonggang, Zheng Yuhui, Wu Baofang, Wu Wenhua

机构信息

Department of Orthopedics, The Second Affiliated Hospital of Fujian Medical University, No. 34 Zhongshan Rd, Licheng District, Quanzhou 362000, China.

出版信息

Biomedicines. 2025 Apr 2;13(4):847. doi: 10.3390/biomedicines13040847.

Abstract

: Osteoporosis (OP) is a prevalent condition marked by reduced bone density and a heightened risk of fractures. Current treatments often have side effects, underscoring the need for safer alternatives. Recent research highlights the significant role of gut microbiota and their metabolites in maintaining bone health. Notably, bacterial outer membrane vesicles (OMVs) have emerged as a promising platform due to their nanoscale sizes, low toxicity, drug-loading capabilities, and excellent biocompatibility. In this study, we developed a delivery system using OMVs derived from (PM). By anchoring bone-targeting peptides to the PM-OMVs membrane, we equipped these vesicles to deliver endogenous miRNAs to the bone microenvironment effectively. The bone-targeted PM-OMVs (PM-OMVs-BT) demonstrated exceptional bone-targeting abilities and exhibited a favorable safety profile in vivo. Additionally, LGG-OMVs-BT were successfully internalized by bone marrow stromal cells (BMSCs) without significant cytotoxicity, effectively promoting their osteogenic differentiation and mineralization. In conclusion, our study indicates that PM-OMVs-BT could offer a safe and effective treatment option for OP.

摘要

骨质疏松症(OP)是一种常见病症,其特征为骨密度降低和骨折风险增加。目前的治疗方法往往存在副作用,这凸显了对更安全替代方案的需求。最近的研究强调了肠道微生物群及其代谢产物在维持骨骼健康方面的重要作用。值得注意的是,细菌外膜囊泡(OMV)因其纳米级尺寸、低毒性、药物装载能力和出色的生物相容性,已成为一个有前景的平台。在本研究中,我们开发了一种使用源自(PM)的OMV的递送系统。通过将骨靶向肽锚定到PM-OMV膜上,我们使这些囊泡能够有效地将内源性miRNA递送至骨微环境。骨靶向PM-OMV(PM-OMVs-BT)表现出卓越的骨靶向能力,并在体内展现出良好的安全性。此外,LGG-OMVs-BT被骨髓基质细胞(BMSC)成功内化,且无明显细胞毒性,有效促进了其成骨分化和矿化。总之,我们的研究表明PM-OMVs-BT可为OP提供一种安全有效的治疗选择。

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