StretchView - A Multi-Axial Cell-Stretching Device for Long-Term Automated Videomicroscopy of Living Cells

被引:0
|
作者
Jaworski, David [1 ,2 ]
Hundsdorfer, Lara [3 ,4 ]
Bastounis, Effie [3 ,4 ]
Constantinou, Iordania [1 ,2 ]
机构
[1] Tech Univ Carolo Wilhelmina Braunschweig, Inst Microtechnol IMT, Alte Salzdahlumer Str 203, D-38124 Braunschweig, Germany
[2] Tech Univ Carolo Wilhelmina Braunschweig, Ctr Pharmaceut Engn PVZ, Franz Liszt Str 35a, D-38106 Braunschweig, Germany
[3] Univ Tubingen, Interfac Inst Microbiol & Infect Med IMIT, Morgenstelle 28, D-72076 Tubingen, Germany
[4] Univ Tubingen, Cluster Excellence Controlling Microbes Fight Infe, EXC 2124, Morgenstelle 28, D-72076 Tubingen, Germany
关键词
cell stretching device; digital image correlation; elastomeric device; live-cell imaging; mechanobiology; INTESTINAL BACTERIAL OVERGROWTH; CYCLIC STRETCH; SHAPE; DIFFERENTIATION; MONOLAYERS; MAGNITUDE; STRESS; DRIVES;
D O I
10.1002/advs.202408853
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Incorporating mechanical stretching of cells in tissue culture is crucial for mimicking (patho)-physiological conditions and understanding the mechanobiological responses of cells, which can have significant implications in areas like tissue engineering and regenerative medicine. Despite the growing interest, most available cell-stretching devices are not compatible with automated live-cell imaging, indispensable for characterizing alterations in the dynamics of various important cellular processes. In this work, StretchView is presented, a multi-axial cell-stretching platform compatible with automated, time-resolved live-cell imaging. Using StretchView, long-term image acquisition of cells in the relaxed and stretched states is shown for the first time (experimental time of 12 h) without the need for human intervention. Homogeneous and stable strain fields are demonstrated for 18 h of cyclic stretching, highlighting the platform's versatility and robustness. As proof-of-principle, the effect of stretching on cell kinematics and spatiotemporal localization of the cell-cell adhesion protein E-cadherin is examined for MDCK cells in monolayer. First evidence of a monotonic increase in junctional E-cadherin localization upon exposure to stretch is presented using live-cell imaging data acquired during cyclic stretching, suggestive of an increase in barrier integrity of the monolayer. These findings highlight the potential of StretchView in providing insights into cell mechanobiology and beyond.
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页数:19
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