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纳秒级电脉冲电场诱导成骨细胞内钙动员。

Nanosecond pulsed electric field induces calcium mobilization in osteoblasts.

机构信息

School of Stomatology, Lanzhou University, Lanzhou 730000, PR China; Center for Biomedical Materials and Tissue Engineering, Academy for Advanced Interdisciplinary Studies, Peking University, Beijing 100871, PR China.

School of Stomatology, Lanzhou University, Lanzhou 730000, PR China.

出版信息

Bioelectrochemistry. 2018 Dec;124:7-12. doi: 10.1016/j.bioelechem.2018.06.009. Epub 2018 Jun 23.

Abstract

Nanosecond pulsed electric field (nsPEF) has the ability to induce a host of intracellular biochemical processes in living cells as a function of parameter setting. In vitro experiments proved that nsPEF stimulation could remarkably promote biomineralization processes and new bone formation. However, the impact of nsPEF parameter settings on the calcium flux of osteoblasts, as well as the intracellular mechanisms underlying those observations have yet to be elucidated. In this study, live osteoblast-like MG63 cells were loaded with fluorescence indicator dye fluo-4 AM. nsPEF stimulation could induce intracellular calcium mobilization in MG63 cells with no refractory period. We confirmed that moderate output voltage (4-8 KV) and large pulse number (25) were required for efficient nsPEF irritation of MG63 cells. Additionally, nsPEF stimulation-induced calcium flux in MG63 cells was dramatically reduced with the treatment by ethylene glycol tetraacetic acid (EGTA), proving that the intake of extracellular calcium ions is crucial for increasing intracellular calcium concentration of nsPEF-treated MG63 cells. Our preliminary study investigated the mechanisms underlying nsPEF stimulation-induced calcium mobilization in osteoblast-like cells, and it has the potential to accelerate the application of nsPEF stimulation in new bone formation.

摘要

纳秒脉冲电场(nsPEF)能够根据参数设置在活细胞中诱导一系列细胞内生化过程。体外实验证明,nsPEF 刺激可以显著促进生物矿化过程和新骨形成。然而,nsPEF 参数设置对成骨细胞钙通量的影响,以及这些观察结果背后的细胞内机制尚未阐明。在这项研究中,活的成骨样 MG63 细胞用荧光指示剂染料 fluo-4 AM 加载。nsPEF 刺激可在无不应期的情况下诱导 MG63 细胞内的钙动员。我们证实,适度的输出电压(4-8KV)和大的脉冲数(25)对于有效地刺激 MG63 细胞是必需的。此外,用乙二胺四乙酸(EGTA)处理后,nsPEF 刺激诱导的 MG63 细胞内钙流显著减少,证明细胞外钙离子的摄取对于增加 nsPEF 处理的 MG63 细胞内的钙离子浓度至关重要。我们的初步研究探讨了 nsPEF 刺激诱导成骨样细胞内钙动员的机制,这有可能加速 nsPEF 刺激在新骨形成中的应用。

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