Schwarz Nicole, Moch Marcin, Windoffer Reinhard, Leube Rudolf E
Institute of Molecular and Cellular Anatomy, RWTH Aachen University, Aachen, Germany.
Institute of Molecular and Cellular Anatomy, RWTH Aachen University, Aachen, Germany.
Methods Enzymol. 2016;568:59-83. doi: 10.1016/bs.mie.2015.07.034. Epub 2015 Nov 3.
Keratin filaments are a hallmark of epithelial differentiation. Their cell type-specific spatial organization and dynamic properties reflect and support epithelial function. To study this interdependency, imaging of fluorescently tagged keratins is a widely used method by which the temporospatial organization and behavior of the keratin intermediate filament network can be analyzed in living cells. Here, we describe methods that have been adapted and optimized to dissect and quantify keratin intermediate filament network dynamics in vital cultured cells and functional tissues.
角蛋白丝是上皮分化的一个标志。它们细胞类型特异性的空间组织和动态特性反映并支持上皮功能。为了研究这种相互依存关系,对荧光标记角蛋白进行成像,是一种广泛使用的方法,通过该方法可以在活细胞中分析角蛋白中间丝网络的时空组织和行为。在这里,我们描述了经过调整和优化的方法,用于剖析和量化重要培养细胞和功能组织中的角蛋白中间丝网络动力学。