Katanosaka Yuki, Naruse Keiji
Department of Cardiovascular Physiology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University.
Clin Calcium. 2010 Apr;20(4):514-9.
Human vascular endothelial cells form the interface between the bloodstream and vessel walls and are continuously subjected to mechanical stimulation. When endothelial cells are stretched cyclically, along one axis, they align perpendicular to the axis of stretch. We previously reported that applying a cyclic, uni-axial strain to cells induced tyrosine phosphorylation of focal adhesion kinase and stimulated mitogen-activated protein kinase. However, it is difficult to quantify and analyze the spatial distribution of tyrosine phosphorylation in these cells, as they form focal adhesions randomly. Recently, we developed a system to overcome this problem by preparing individual, uniform, patterned cells that could be stretched cyclically and uni-axially. In this system we were able to statistically analyze cellular responses in these patterned cells, when subjected to a cyclic, uni-axial strain, using fluorescent microscopy.
人类血管内皮细胞构成了血流与血管壁之间的界面,并不断受到机械刺激。当内皮细胞沿一个轴进行周期性拉伸时,它们会垂直于拉伸轴排列。我们之前报道过,对细胞施加周期性单轴应变会诱导粘着斑激酶的酪氨酸磷酸化,并刺激丝裂原活化蛋白激酶。然而,由于这些细胞随机形成粘着斑,因此难以量化和分析这些细胞中酪氨酸磷酸化的空间分布。最近,我们开发了一种系统来克服这个问题,即制备能够进行周期性单轴拉伸的单个、均匀、有图案的细胞。在这个系统中,当对这些有图案的细胞施加周期性单轴应变时,我们能够使用荧光显微镜对细胞反应进行统计分析。