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细胞大小、环境条件和生长阶段对环境扫描电子显微镜内单个W303酵母细胞强度的影响。

The effects of cell sizes, environmental conditions, and growth phases on the strength of individual W303 yeast cells inside ESEM.

作者信息

Ahmad Mohd Ridzuan, Nakajima Masahiro, Kojima Seiji, Homma Michio, Fukuda Toshio

机构信息

Department of Micro-Nano Systems Engineering, Nagoya University, Nagoya 464-8603, Japan.

出版信息

IEEE Trans Nanobioscience. 2008 Sep;7(3):185-93. doi: 10.1109/TNB.2008.2002281.

DOI:10.1109/TNB.2008.2002281
PMID:18779098
Abstract

We performed in situ measurements of mechanical properties of individual W303 wild-type yeast cells by using an integrated environmental scanning electron microscope (ESEM)-nanomanipulator system. Compression experiments to penetrate the cell walls of single cells of different cell sizes (about 3-6 micro m diameter), environmental conditions (600 Pa and 3 mPa), and growth phases (early log, mid log, late log and saturation) were conducted. The compression experiments were performed inside ESEM, embedded with a 7 DOF nanomanipulator with a sharp pyramidal end effector and a cooling stage, i.e., a temperature controller. ESEM itself can control the chamber pressure. Data clearly show an increment in penetration force, i.e., 96 +/- 2, 124 +/- 10, 163 +/- 1, and 234 +/- 14 nN at 3, 4, 5, and 6 micro m cell diameters, respectively. Whereas, 20-fold increase in penetration forces was recorded at different environmental conditions for 5 micro m cell diameter, i.e., 163 +/- 1 nN and 2.95 +/- 0.23 mu N at 600 Pa (ESEM mode) and 3 mPa (HV mode), respectively. This was further confirmed from quantitative estimation of average cell rigidity through the Hertz model, i.e., ESEM mode (3.31 +/- 0.11 MPa) and HV mode (26.02 +/- 3.66 MPa) for 5 micro m cell diameter. Finally, the penetration forces at different cell growth phases also show the increment pattern from log (early, mid, and late) to saturation phases, i.e., 161 +/- 25, 216 +/- 15, 255 +/- 21, and 408 +/- 41 nN, respectively.

摘要

我们使用集成环境扫描电子显微镜(ESEM)-纳米操纵器系统对单个W303野生型酵母细胞的力学性能进行了原位测量。对不同细胞大小(直径约3-6微米)、环境条件(600帕和3毫帕)以及生长阶段(对数早期、对数中期、对数后期和饱和期)的单细胞进行了细胞壁穿透压缩实验。压缩实验在ESEM内部进行,该设备配备了一个带有尖锐金字塔形末端执行器的7自由度纳米操纵器和一个冷却台,即温度控制器。ESEM本身可以控制腔室压力。数据清楚地显示出穿透力的增加,即细胞直径为3、4、5和6微米时,穿透力分别为96±2、124±10、163±1和234±14纳牛。然而,对于直径为5微米的细胞,在不同环境条件下记录到穿透力增加了20倍,即在600帕(ESEM模式)和3毫帕(高压模式)下分别为163±1纳牛和2.95±0.23微牛。通过赫兹模型对平均细胞刚度进行定量估计进一步证实了这一点,即对于直径为5微米的细胞,ESEM模式下为(3.31±0.11兆帕),高压模式下为(26.02±3.66兆帕)。最后,不同细胞生长阶段的穿透力也呈现出从对数期(早期、中期和后期)到饱和期的增加模式,即分别为161±25、216±15、255±21和408±41纳牛。

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