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杆菌肽通过刺激骨形态发生蛋白 2/Smad 轴促进人骨髓间充质干细胞的成骨分化。

Bacitracin promotes osteogenic differentiation of human bone marrow mesenchymal stem cells by stimulating the bone morphogenetic protein-2/Smad axis.

机构信息

Department of Bone and Joint Surgery, Renji Hospital, Shanghai Jiaotong University School of Medicine, PR China.

Department of Bone and Joint Surgery, Renji Hospital, Shanghai Jiaotong University School of Medicine, PR China.

出版信息

Biomed Pharmacother. 2018 Jul;103:588-597. doi: 10.1016/j.biopha.2018.04.084. Epub 2018 Apr 24.

Abstract

Bacitracin, a widely used metallopeptide antibiotic, has been reported to be locally used in treating wounds without systemic adverse reactions. Our preliminary study showed that bacitracin might enhance the osteogenic differentiation of human bone marrow mesenchymal stem cells (HBMSCs). The present study investigated whether bacitracin affects the osteogenic differentiation of HBMSCs and the molecular mechanisms involved. The proliferation of HBMSCs in the presence of bacitracin was examined using a cell counting kit-8 (CCK-8) assay. The effects of bacitracin on the cell cycle and apoptosis of HBMSCs were observed using flow cytometry assay. Staining and quantitative assays for alkaline phosphatase (ALP) staining, collagen deposition (Sirius Red), and mineralization (Alizarin Red) were used to study osteogenic differentiation of HBMSCs. The expression of osteogenic differentiation markers was detected using quantitative reverse transcription polymerase chain reaction (RT-qPCR) analyses. The activation of related signaling pathways was examined using a luciferase reporter assay and western blotting. Bacitracin treatment increased osteogenic differentiation of HBMSCs without cytotoxicity and did not adversely affect cell cycle progression or apoptosis. The luciferase reporter assay showed that bacitracin activated the transcription of bone morphogenetic protein-2 (BMP2) gene, a key gene in the BMP2/Smad signaling axis. Western blotting indicated that this axis was markedly activated by bacitracin stimulation of osteogenesis. Moreover, the activation of Smad phosphorylation and osteogenic differentiation by bacitracin was inhibited by a transforming growth factor (TGF)-β/Smad inhibitor (LDN-193189 HCl) and small interfering RNA (siRNA) gene silencing (si-BMP2). In conclusion, our results suggest that bacitracin can promote osteogenesis of HBMSCs by activating the BMP2/Smad signaling axis.

摘要

杆菌肽是一种广泛应用的金属肽抗生素,据报道其可局部用于治疗伤口,而无全身不良反应。我们的初步研究表明杆菌肽可能增强人骨髓间充质干细胞(HBMSCs)的成骨分化。本研究探讨了杆菌肽是否影响 HBMSCs 的成骨分化及其涉及的分子机制。使用细胞计数试剂盒-8(CCK-8)检测杆菌肽存在时 HBMSCs 的增殖。使用流式细胞术检测杆菌肽对 HBMSCs 细胞周期和凋亡的影响。使用碱性磷酸酶(ALP)染色、胶原蛋白沉积(天狼星红)和矿化(茜素红)染色和定量分析来研究 HBMSCs 的成骨分化。使用定量逆转录聚合酶链反应(RT-qPCR)分析检测成骨分化标志物的表达。使用荧光素酶报告基因检测和 Western blot 检测相关信号通路的激活。杆菌肽处理增加了 HBMSCs 的成骨分化,而无细胞毒性,且不会对细胞周期进程或凋亡产生不利影响。荧光素酶报告基因检测显示,杆菌肽激活了骨形态发生蛋白-2(BMP2)基因的转录,BMP2/Smad 信号轴中的关键基因。Western blot 表明,该信号轴在杆菌肽刺激成骨过程中被显著激活。此外,转化生长因子(TGF)-β/Smad 抑制剂(LDN-193189 HCl)和小干扰 RNA(siRNA)基因沉默(si-BMP2)抑制了杆菌肽对 Smad 磷酸化和成骨分化的激活。综上所述,我们的结果表明杆菌肽可通过激活 BMP2/Smad 信号轴促进 HBMSCs 的成骨作用。

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