Department of Chemical & Biomolecular Engineering, University of Nebraska-Lincoln, Lincoln, NE, USA.
Ultrasound Med Biol. 2013 Jul;39(7):1303-19. doi: 10.1016/j.ultrasmedbio.2013.01.015. Epub 2013 Apr 3.
This study provides evidence that low-intensity ultrasound directly affects nuclear processes, and the magnitude of the effect varies with frequency. In particular, we show that the transcriptional induction of first load-inducible genes, which is independent of new protein synthesis, is frequency dependent. Bovine chondrocytes were exposed to low-intensity (below the cavitational threshold) ultrasound at 2, 5 and 8 MHz. Ultrasound elevated the expression of early response genes c-Fos, c-Jun and c-Myc, maximized at 5 MHz. The phosphorylated ERK inhibitor PD98059 abrogated any increase in c-series gene expression, suggesting that signaling occurs via the MAPPK/ERK pathway. However, phosphorylated ERK levels did not change with ultrasound frequency, indicating that processes downstream of ERK phosphorylation (such as nuclear transport and chromatin reorganization) respond to ultrasound with frequency dependence. A quantitative, biphasic mathematical model based on Biot theory predicted that cytoplasmic and nuclear stress is maximized at 5.2 ± 0.8 MHz for a chondrocyte, confirming experimental measurements.
这项研究提供了证据表明,低强度超声直接影响核过程,并且影响的大小随频率而变化。特别是,我们表明,新蛋白质合成独立的第一负载诱导基因的转录诱导,是频率依赖的。牛软骨细胞在 2、5 和 8MHz 的低强度(低于空化阈值)超声下暴露。超声使早期反应基因 c-Fos、c-Jun 和 c-Myc 的表达升高,在 5MHz 时达到最大值。磷酸化的 ERK 抑制剂 PD98059 消除了 c 系列基因表达的任何增加,表明信号通过 MAPPK/ERK 途径发生。然而,磷酸化 ERK 水平随超声频率没有变化,表明 ERK 磷酸化下游的过程(如核转运和染色质重排)对超声具有频率依赖性的反应。基于 Biot 理论的定量、双相数学模型预测,对于软骨细胞,细胞质和核应力在 5.2±0.8MHz 时达到最大值,与实验测量结果一致。