Liu Yunbo, Kon Takashi, Li Chuanyuan, Zhong Pei
Department of Mechanical Engineering and Materials Science, Duke University, Durham, North Carolina 27708, USA.
J Acoust Soc Am. 2005 Nov;118(5):3328-36. doi: 10.1121/1.2041247.
Cultured human cervical cancer (HeLa) and rat mammary carcinoma (R3230Ac) cells were transfected with vectors encoding green fluorescent protein (GFP) under the control of hsp70B promoter. Aliquots of 10-microl transfected cells (5 x 10(7) cells/ml) were placed in 0.2-ml thin-wall polymerase chain reaction tubes and exposed to 1.1-MHz high intensity focused ultrasound (HIFU) at a peak negative pressure P- = 2.68 MPa. By adjusting the duty cycle of the HIFU transducer, the cell suspensions were heated to a peak temperature from 50 to 70 degrees C in 1-10 s. Exposure dependent cell viability and gene activation were evaluated. For a 5-s HIFU exposure, cell viability dropped from 95% at 50 degrees C to 13% at 70 degrees C. Concomitantly, gene activation in sublethally injured tumor cells increased from 4% at 50 degrees C to 41% at 70 degrees C. A similar trend was observed at 60 degrees C peak temperature as the exposure time increased from 1 to 5 s. Further increase of exposure duration to 10 s led to significantly reduced cell viability and lower overall gene activation in exposed cells. Altogether, maximum HIFU-induced gene activation was achieved at 60 degrees C in 5 s. Under these experimental conditions, HIFU-induced gene activation was found to be produced primarily by thermal rather than mechanical stresses.
将编码绿色荧光蛋白(GFP)且受hsp70B启动子控制的载体转染至培养的人宫颈癌(HeLa)细胞和大鼠乳腺癌(R3230Ac)细胞。将10微升转染细胞的等分试样(5×10⁷个细胞/毫升)置于0.2毫升薄壁聚合酶链反应管中,并在峰值负压P- = 2.68兆帕下暴露于1.1兆赫的高强度聚焦超声(HIFU)。通过调节HIFU换能器的占空比,将细胞悬液在1至10秒内加热至50至70摄氏度的峰值温度。评估暴露依赖性细胞活力和基因激活情况。对于5秒的HIFU暴露,细胞活力从50摄氏度时的95%降至70摄氏度时的13%。与此同时,亚致死性损伤肿瘤细胞中的基因激活从50摄氏度时的4%增加至70摄氏度时的41%。当峰值温度为60摄氏度且暴露时间从1秒增加到5秒时,观察到类似趋势。将暴露持续时间进一步增加至10秒导致暴露细胞的细胞活力显著降低且总体基因激活水平降低。总之,在60摄氏度下暴露5秒可实现最大的HIFU诱导基因激活。在这些实验条件下,发现HIFU诱导的基因激活主要由热应力而非机械应力产生。