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Stepwise Administration of Bone-Targeted Lipid Nanoparticles Encapsulating Valproic Acid and TUDCA Facilitates In Vivo Direct Reprogramming for Osteoporosis Treatmentopen access

Authors
Park, HyoeunCho, Woong JinKim, JiseongChoi, HyejongBaek, InhoKim, YoungjinKim, DeogilKim, Byoung JuArai, YoshieLee, Soo-Hong
Issue Date
Aug-2025
Publisher
한국조직공학과 재생의학회
Keywords
Mouse fibroblasts; Stepwise treatment; Direct reprogramming; Bone-targeted lipid nanoparticles; Osteoporosis
Citation
조직공학과 재생의학, v.22, no.6, pp 831 - 845
Pages
15
Indexed
SCIE
SCOPUS
KCI
Journal Title
조직공학과 재생의학
Volume
22
Number
6
Start Page
831
End Page
845
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/58607
DOI
10.1007/s13770-025-00738-5
ISSN
1738-2696
2212-5469
Abstract
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.Graphical abstractStepwise administration of VPA-LNPs and TUDCA-LNPs enhances In vivo direct reprogramming for osteoporosis therapy.
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