银纳米粒子在体外促进小鼠胚胎成纤维细胞的成骨分化。

IF 1.5 Q4 CELL BIOLOGY American journal of stem cells Pub Date : 2023-08-15 eCollection Date: 2023-01-01
Juan Du, Xuelai Liu, Carol Wing Yan Wong, Chun-Nam Lok, Zhen Yang, Zhixin Yuan, Kenneth Kak Yuen Wong
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摘要

目的:研究银纳米粒子(AgNps)是否能促进小鼠胚胎成纤维细胞的增殖和成骨分化。方法:将小鼠胚胎成纤维细胞分为两组:第一组在DMEM/F12培养基中培养,第二组在成骨培养基中培育。然后用16、32或100μM AgNps对两组进行治疗。使用BrdU和MTT法在不同时间点测量成纤维细胞的增殖和活力。测定茜素红染色和碱性磷酸酶(ALP)活性,观察成纤维细胞向成骨细胞分化。蛋白质组学(细胞因子阵列)用于检测分化过程中的111种不同细胞因子。结果:AgNps在16μM浓度下刺激小鼠胚胎成纤维细胞增殖。与未培养AgNps的细胞相比,在用AgNps培养的细胞中观察到钙矿化的显著增强。第2组细胞在细胞密度高的中心周围显示结节。在成骨培养基中培养的小鼠胚胎成纤维细胞的ALP活性在整个培养期内增加。在第7天和第14天,添加浓度为32μM和100μM的AgNps诱导了更高的ALP活性。蛋白质组学阵列结果显示,在含有16μM AgNPs的培养基中,低密度脂蛋白受体(LDL-R)和前蛋白转化酶枯草杆菌蛋白酶/可辛9型(PCSK-9)显著增加,而骨保护素(OPG)显著降低。LDL-R和PCSK-9以及OPG可能在这一过程中发挥关键作用。
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Silver nanoparticles promote osteogenic differentiation of mouse embryonic fibroblasts in vitro.

Objective: This study investigated if silver nanoparticles (AgNps) could promote the proliferation and osteogenic differentiation of mouse embryonic fibroblasts.

Methods: Mouse embryonic fibroblasts were divided into two groups: Group 1 cells were cultured in DMEM/F12 medium and Group 2 cells were cultured in osteogenic medium. Both groups were then treated with 16, 32, or 100 μM AgNps. Fibroblast proliferation and viability were measured using BrdU and MTT methods at varying time points. Alizarin red staining and alkaline phosphatase (ALP) activity were measured to observe fibroblast differentiation into osteoblasts. Proteomics (cytokine array) was used to detect 111 different cytokines during differentiation.

Results: AgNps stimulated proliferation of mouse embryonic fibroblasts at a concentration of 16 μM. Marked enhancement of calcium mineralization was observed in cells cultured with AgNps compared with cells cultured without AgNps. Group 2 cells displayed nodules around the center where the cell density was high. ALP activity of mouse embryonic fibroblasts cultured in osteogenic medium increased during the whole culture period. Addition of AgNps at concentrations of 32 μM and 100 μM induced higher ALP activity at days 7 and 14. Proteomic array results show that low density lipoprotein receptor (LDL-R) and proprotein convertase subtilisin/kexin type 9 (PCSK-9) were significantly increased, while osteoprotegerin (OPG) was significantly reduced in medium containing 16 μM AgNPs.

Conclusion: AgNps could promote differentiation of mouse embryonic fibroblasts into osteoblastic cells. LDL-R and PCSK-9, as well as OPG, may play a critical role in this process.

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