逐步给药骨靶向脂质纳米颗粒包封丙戊酸和TUDCA促进体内直接重编程治疗骨质疏松症。

IF 4.4 4区 医学 Q2 CELL & TISSUE ENGINEERING
Hyoeun Park, Woong Jin Cho, Jiseong Kim, Hyejong Choi, Inho Baek, Youngjin Kim, Deogil Kim, Byoung Ju Kim, Yoshie Arai, Soo-Hong Lee
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引用次数: 0

摘要

背景:再生医学的最终目标是将体内受损组织恢复到健康状态。直接重编程,也称为转分化,通过将大量体细胞(如成纤维细胞)转化为功能不同的细胞类型来进行组织再生,具有重要的治疗潜力。尽管在再生医学中有潜在的应用,但直接重编程面临着效率低和体内适用性差等主要挑战。在这项研究中,我们提出了一种新的骨质疏松症治疗策略,该策略基于体内直接重编程,采用循序渐进的递送方法,首先增强细胞干性,随后诱导成骨转分化。增强谱系承诺细胞的干性有助于它们转化为其他功能细胞类型。方法:以丙戊酸(VPA)和牛磺酸去氧胆酸(TUDCA)分别作为重编程因子和促骨因子,考察通过分步给药直接重编程的效率。VPA增加了Oct4、Nanog、Sox2等干性基因的表达,随后的TUDCA处理增强了小鼠成纤维细胞中成骨基因的表达。利用双膦酸盐(BP)偶联脂质纳米颗粒作为载体,将这些因子靶向递送到骨组织周围的成纤维细胞,从而实现随后直接重编程成成骨细胞。结果:我们的研究结果表明,通过逐步给药VPA和TUDCA,顺序诱导细胞重编程和组织再生,与同时给药相比,显著提高了骨质疏松小鼠模型的治疗效果。结论:这种逐步骨靶向给药系统通过体内直接重编程为骨质疏松症治疗提供了一种很有前景的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Stepwise Administration of Bone-Targeted Lipid Nanoparticles Encapsulating Valproic Acid and TUDCA Facilitates In Vivo Direct Reprogramming for Osteoporosis Treatment.

Background: The ultimate goal of regenerative medicine is to restore damaged tissues to a healthy state in the body. Direct reprogramming, also referred to as transdifferentiation, holds significant therapeutic potential by converting abundant somatic cells, such as fibroblasts, into functionally distinct cell types for tissue regeneration. Despite its potential applications in regenerative medicine, direct reprogramming faces major challenges, including low efficiency and poor In vivo applicability. In this study, we propose a novel therapeutic strategy for osteoporosis based on In vivo direct reprogramming using a stepwise delivery approach that first enhances cellular stemness and subsequently induces osteogenic transdifferentiation. Enhancing stemness in lineage-committed cells facilitates their conversion into other functional cell types.

Method: To investigate the efficiency of direct reprogramming via stepwise delivery, we utilized valproic acid (VPA) and tauroursodeoxycholic acid (TUDCA) as reprogramming and bone-stimulating factors, respectively. VPA increased the expression of stemness genes, including Oct4, Nanog, and Sox2, and subsequent treatment of TUDCA enhanced the expression of osteogenic genes in the mouse fibroblast. Targeted delivery of these factors to fibroblasts surrounding bone tissue, enabling subsequent direct reprogramming into osteoblasts, was achieved using bisphosphonate (BP)-conjugated lipid nanoparticles as carriers.

Results: Our findings demonstrate that sequential induction of cell reprogramming and tissue regeneration through stepwise administration of VPA and TUDCA significantly enhances therapeutic efficacy in a mouse model of osteoporosis compared to their simultaneous administration.

Conclusion: This stepwise bone-targeted drug delivery system presents a promising strategy for osteoporosis treatment via In vivo direct reprogramming.

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来源期刊
Tissue engineering and regenerative medicine
Tissue engineering and regenerative medicine CELL & TISSUE ENGINEERING-ENGINEERING, BIOMEDICAL
CiteScore
6.80
自引率
5.60%
发文量
83
审稿时长
6-12 weeks
期刊介绍: Tissue Engineering and Regenerative Medicine (Tissue Eng Regen Med, TERM), the official journal of the Korean Tissue Engineering and Regenerative Medicine Society, is a publication dedicated to providing research- based solutions to issues related to human diseases. This journal publishes articles that report substantial information and original findings on tissue engineering, medical biomaterials, cells therapy, stem cell biology and regenerative medicine.
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