Garaschuk Olga, Griesbeck Oliver, Konnerth Arthur
Institute of Neuroscience, Technical University Munich, Biedersteinerstr. 29, 80802 Munich, Germany.
Cell Calcium. 2007 Oct-Nov;42(4-5):351-61. doi: 10.1016/j.ceca.2007.02.011. Epub 2007 Apr 23.
Fluorescence imaging represents a powerful approach for the detection of intracellular Ca(2+) signals in vivo. With appropriate techniques, Ca(2+) signals can be recorded at many levels of complexity, ranging from large scale neuronal networks down to individual presynaptic boutons or postsynaptic spines. Here we review the applicability of genetically encoded Ca(2+) indicators for in vivo Ca(2+) imaging of neural function. We describe some of the recent progress in sensor design and evaluate the performance of the new family of Troponin C-based Ca(2+) indicators. Further, we analyze properties of Ca(2+) biosensors transgenically expressed in various experimental animal models and illustrate their use for measuring somatic and dendritic Ca(2+) signals in neurons of the mammalian brain.
荧光成像代表了一种在体内检测细胞内钙离子(Ca(2+))信号的强大方法。通过适当的技术,可以在多种复杂程度的层面上记录Ca(2+)信号,从大规模神经网络到单个突触前终扣或突触后棘。在这里,我们综述了基因编码的Ca(2+)指示剂在神经功能体内Ca(2+)成像中的适用性。我们描述了传感器设计方面的一些最新进展,并评估了基于肌钙蛋白C的新型Ca(2+)指示剂家族的性能。此外,我们分析了在各种实验动物模型中转基因表达的Ca(2+)生物传感器的特性,并说明了它们在测量哺乳动物大脑神经元的体细胞和树突状Ca(2+)信号中的应用。