Bone Regeneration Enhanced by Quercetin-Capped Selenium Nanoparticles via miR206/Connexin43, WNT, and BMP signaling pathways.

IF 7 2区 医学 Q1 GERIATRICS & GERONTOLOGY
Garima Sharma, Yeon Hee Lee, Jin-Chul Kim, Ashish Ranjan Sharma, Sang-Soo Lee
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引用次数: 0

Abstract

Age-related alterations in the skeletal system are linked to decreased bone mass, a reduction in bone strength and density, and an increased risk of fractures and osteoporosis. Therapeutics are desired to stimulate bone regeneration and restore imbalance in the bone remodeling process. Quercetin (Qu), a naturally occurring flavonoid, induces osteogenesis; however, its solubility, stability, and bioavailability limit its therapeutic use. Nanoformulation can improve the physical properties of Qu and enhance its bioactivity and bioavailability. Further, localized delivery of Qu nanoformulations at the site of bone defects could ensure high local concentration, augmenting its osteogenic properties. Thus, this study aims to synthesize selenium nanoparticles-based Qu nanoformulation (Qu-SeNPs) and evaluate their osteogenic stimulation ability along with localized bone regeneration ability. Here, the spontaneously synthesized Qu-SeNPs showed uniform size distribution and rough flower-shaped morphology. The confocal images indicate improved cellular uptake and even cellular distribution of Qu-SeNPs in osteoblasts, resulting in increased osteogenic activity as indicated by enhanced expression of early and late osteoprogenitor differentiation markers. Qu-SeNPs also decreased osteoblasts' RANKL/OPG ratio and inhibited osteoclast formation. Mechanistically, Qu-SeNPs activate critical signaling pathways, including WNT and BMP, and utilize the miR-206/Connexin43 pathway to enhance osteogenesis. In vivo, experiments utilizing a drill-hole bone defect model in mice indicate that hydrogel-mediated localized delivery of Qu-SeNPs significantly accelerates bone defect healing. Thus, well-characterized and mechanistic, detailed synthesized Qu-SeNPs can restore bone remodeling, and Qu-SeNPs embedded in hydrogels may improve Qu cellular uptake and bioavailability in clinical settings, enabling innovative orthopedic and regenerative therapies for bone loss/defects.

槲皮素覆盖的硒纳米粒子通过miR206/Connexin43、WNT和BMP信号通路促进骨再生。
与年龄相关的骨骼系统改变与骨量减少、骨强度和密度降低以及骨折和骨质疏松症的风险增加有关。治疗方法需要刺激骨再生和恢复骨重塑过程中的不平衡。槲皮素(Qu)是一种天然存在的类黄酮,可诱导成骨;然而,其溶解度、稳定性和生物利用度限制了其治疗用途。纳米制剂可以改善曲的物理性质,提高其生物活性和生物利用度。此外,在骨缺损部位局部递送Qu纳米制剂可以确保高局部浓度,增强其成骨特性。因此,本研究旨在合成基于硒纳米颗粒的Qu纳米制剂(Qu- senps),并评估其成骨刺激能力和局部骨再生能力。在这里,自发合成的q - senps具有均匀的大小分布和粗糙的花状形态。共聚焦图像显示,成骨细胞中Qu-SeNPs的细胞摄取甚至细胞分布都有所改善,导致成骨活性增加,这可以通过增强早期和晚期成骨祖细胞分化标志物的表达来证明。q - senps还能降低成骨细胞的RANKL/OPG比值,抑制破骨细胞的形成。机制上,q - senps激活关键信号通路,包括WNT和BMP,并利用miR-206/Connexin43通路促进成骨。在体内,利用小鼠钻孔骨缺损模型进行的实验表明,水凝胶介导的局部递送Qu-SeNPs可显著加速骨缺损愈合。因此,具有良好特征和机制的详细合成的Qu- senps可以恢复骨重塑,并且嵌入水凝胶中的Qu- senps可以改善临床环境中的Qu细胞摄取和生物利用度,从而实现骨丢失/骨缺损的创新骨科和再生治疗。
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来源期刊
Aging and Disease
Aging and Disease GERIATRICS & GERONTOLOGY-
CiteScore
14.60
自引率
2.70%
发文量
138
审稿时长
10 weeks
期刊介绍: Aging & Disease (A&D) is an open-access online journal dedicated to publishing groundbreaking research on the biology of aging, the pathophysiology of age-related diseases, and innovative therapies for conditions affecting the elderly. The scope encompasses various diseases such as Stroke, Alzheimer's disease, Parkinson’s disease, Epilepsy, Dementia, Depression, Cardiovascular Disease, Cancer, Arthritis, Cataract, Osteoporosis, Diabetes, and Hypertension. The journal welcomes studies involving animal models as well as human tissues or cells.
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