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用于监测成骨分化过程中细胞碱性磷酸酶活性的智能表面增强共振拉曼散射纳米探针

Smart Surface-Enhanced Resonance Raman Scattering Nanoprobe for Monitoring Cellular Alkaline Phosphatase Activity during Osteogenic Differentiation.

作者信息

Sun Dan, Xu Weiqing, Liang Chongyang, Shi Wei, Xu Shuping

机构信息

State Key Laboratory of Supramolecular Structure and Materials, Institute of Theoretical Chemistry, Jilin University, Changchun 130012, PR China.

Institute of Frontier Medical Science, Jilin University, Changchun 130021, PR China.

出版信息

ACS Sens. 2020 Jun 26;5(6):1758-1767. doi: 10.1021/acssensors.0c00428. Epub 2020 May 19.

Abstract

High-efficiency induction of bone marrow mesenchymal stem cells (BMSCs) to osteogenic differentiation in vitro can help solve a series of bone diseases such as bone injury, fracture repair, and osteoporosis. In order to explore the optimal conditions for different chemical inducers to promote BMSCs differentiation and the possible differentiation mechanisms, we developed a smart nanoprobe that can achieve in situ alkaline phosphatase (ALP) activity detection during osteogenic differentiation in cells. The smart nanoprobe (Au@BCIP) was designed as the surface decoration of gold nanoparticles (AuNPs) with 5-bromo-4-chloro-3-indolyl phosphate (BCIP). The nanoprobe was co-cultured with differentiated BMSCs at different stages to monitor ALP activity based on an ALP-catalyzed hydrolysis reaction with BCIP as a substrate. The product can be quickly oxidized by dissolved oxygen to obtain a Raman-active species (5,5'-dibromo-4,4'-dichloro-1,1-[2,2'] biindolylidene-3,3'-dione). The SERS sensitivity was greatly improved by resonating the excitation wavelength of 632.8 nm. It is a new strategy for tracing bone disease-related ALP activity in an model with high sensitivity and selectivity and non-invasion. By using this nanoprobe, osteogenic differentiation of cells under osteogenic supplements was assessed and the p38 MAPK signaling pathway for osteogenic differentiation was experimentally evidenced, which are of significance for understanding BMSCs and regulating their osteogenic differentiation process.

摘要

高效诱导骨髓间充质干细胞(BMSCs)在体外向成骨分化有助于解决一系列骨疾病,如骨损伤、骨折修复和骨质疏松症。为了探索不同化学诱导剂促进BMSCs分化的最佳条件以及可能的分化机制,我们开发了一种智能纳米探针,它可以在细胞成骨分化过程中实现原位碱性磷酸酶(ALP)活性检测。智能纳米探针(Au@BCIP)设计为用5-溴-4-氯-3-吲哚基磷酸酯(BCIP)对金纳米颗粒(AuNPs)进行表面修饰。该纳米探针与不同阶段分化的BMSCs共培养,以基于以BCIP为底物的ALP催化水解反应监测ALP活性。产物可被溶解氧快速氧化,得到一种具有拉曼活性的物质(5,5'-二溴-4,4'-二氯-1,1-[2,2']联吲哚亚基-3,3'-二酮)。通过使激发波长共振到632.8 nm,表面增强拉曼光谱(SERS)灵敏度得到极大提高。这是一种在模型中以高灵敏度、高选择性和非侵入性追踪骨疾病相关ALP活性的新策略。通过使用这种纳米探针,评估了成骨补充剂作用下细胞的成骨分化,并通过实验证明了成骨分化的p38丝裂原活化蛋白激酶(MAPK)信号通路,这对于理解BMSCs和调节其成骨分化过程具有重要意义。

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