Gerstmair Axel, Fois Giorgio, Innerbichler Siegfried, Dietl Paul, Felder Edward
Institute for General Physiology/M-25, University of Ulm, Albert Einstein Allee 11, 89081 Ulm, Germany.
J Appl Physiol (1985). 2009 Aug;107(2):613-20. doi: 10.1152/japplphysiol.00012.2009. Epub 2009 Jun 4.
Mechanical stimuli control multiple cellular processes such as secretion, growth, and differentiation. A widely used method to investigate cell strain ex vivo is stretching an elastic membrane to which cells adhere. However, simultaneous imaging of dynamic signals from single living cells grown on elastic substrates during uni-axial changes of cell length is usually hampered by the movement of the sample along the strain axis out of the narrow optical field of view. We used a thin, prestrained, elastic chamber as growth substrate for the cells and deformed the chamber with a computer-controlled stretch device. An algorithm that compensates the lateral displacement during stretch kept any selected point of the whole chamber at a constant position on the microscope during strain or relaxation (compression). Adherent cells or other materials that adhere to the bottom of the chamber at any given position could be imaged during controlled positive (stretch) or negative (compression) changes of cell length. The system was tested on living alveolar type II cells, in which mechanical effects on secretion have been intensively investigated in the past.
机械刺激控制多种细胞过程,如分泌、生长和分化。一种广泛用于体外研究细胞应变的方法是拉伸细胞所附着的弹性膜。然而,在细胞长度单轴变化期间,对生长在弹性基质上的单个活细胞的动态信号进行同步成像通常会受到样品沿应变轴移出狭窄光学视野的运动的阻碍。我们使用一个薄的、预拉伸的弹性腔室作为细胞的生长基质,并用计算机控制的拉伸装置使腔室变形。一种在拉伸过程中补偿横向位移的算法,在应变或松弛(压缩)过程中,使整个腔室的任何选定的点在显微镜上保持恒定位置。在细胞长度的受控正(拉伸)或负(压缩)变化期间,可以对在任何给定位置附着在腔室底部的贴壁细胞或其他材料进行成像。该系统在活的肺泡II型细胞上进行了测试,过去对其分泌的机械效应进行了深入研究。