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两种新型近红外荧光探针有望成为骨修复成像的工具。

Two new, near-infrared, fluorescent probes as potential tools for imaging bone repair.

机构信息

Graduate Institute of Medical Sciences, College of Medicine, Taipei Medical University, Taipei, Taiwan.

Department of Biomedical Engineering, Chung Yuan Christian University, Chung-Li, Taiwan.

出版信息

Sci Rep. 2020 Feb 13;10(1):2580. doi: 10.1038/s41598-020-59522-1.

Abstract

A precise imaging technique to evaluate osteogenesis, osteodifferentiation, and osseointegration following peri-implant surgery is in high clinical demand. Herein, we report the generation of two new, near-infrared (NIR) fluorescent probes for use in the molecular imaging of bone repair. The first probe aims to monitor the in vitro differentiation of human mesenchymal stem cells (MSCs) into osteoblasts. A NIR fluorochrome was conjugated to a cyclic peptide that binds to integrin α5β1, a factor that promotes osteogenesis in MSCs and therefore functioned as an osteoblast-specific marker. The second probe aims to monitor osteogenesis, and was generated by conjugating the drug pamidronate to a NIR fluorescent gold nanocluster. Pamidronate specifically binds to hydroxyapatite (HA), a mineral present in bone that is produced by osteoblasts, and therefore provides a functional marker for new bone formation. Our results show that both probes bind to their specific targets in vitro-differentiated osteoblasts, and not to undifferentiated MSCs, and emit NIR fluorescence for functional detection. This in vitro work demonstrates the ability of these probes to bind to active osteoblasts and their mineral deposits and highlight their potential utility as clinical tools for the imaging of the osseointegration process at the molecular level.

摘要

一种精确的成像技术,用于评估种植体周围手术后的成骨、成骨分化和骨整合,具有很高的临床需求。在此,我们报告了两种新的近红外(NIR)荧光探针的生成,用于骨修复的分子成像。第一个探针旨在监测人骨髓间充质干细胞(MSCs)向成骨细胞的体外分化。将 NIR 荧光团连接到与整合素 α5β1 结合的环肽上,整合素 α5β1 是促进 MSCs 成骨的因素,因此作为成骨细胞特异性标志物发挥作用。第二个探针旨在监测成骨作用,并通过将药物帕米膦酸盐与 NIR 荧光金纳米簇缀合来生成。帕米膦酸盐特异性结合到羟基磷灰石(HA),即成骨细胞产生的存在于骨骼中的矿物质,因此为新骨形成提供了功能标志物。我们的结果表明,两种探针都与体外分化的成骨细胞的特定靶标结合,而不与未分化的 MSCs 结合,并发出 NIR 荧光进行功能检测。这项体外工作表明,这些探针能够与活性成骨细胞及其矿物质沉积物结合,并突出了它们作为临床工具在分子水平上对骨整合过程进行成像的潜在用途。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8756/7018698/f17957aa8029/41598_2020_59522_Fig1_HTML.jpg

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