Baker B J, Mutoh H, Dimitrov D, Akemann W, Perron A, Iwamoto Y, Jin L, Cohen L B, Isacoff E Y, Pieribone V A, Hughes T, Knöpfel T
Department of Cellular and Molecular Physiology, Yale University School of Medicine, New Haven, CT 06520, USA.
Brain Cell Biol. 2008 Aug;36(1-4):53-67. doi: 10.1007/s11068-008-9026-7. Epub 2008 Aug 5.
Imaging activity of neurons in intact brain tissue was conceived several decades ago and, after many years of development, voltage-sensitive dyes now offer the highest spatial and temporal resolution for imaging neuronal functions in the living brain. Further progress in this field is expected from the emergent development of genetically encoded fluorescent sensors of membrane potential. These fluorescent protein (FP) voltage sensors overcome the drawbacks of organic voltage sensitive dyes such as non-specificity of cell staining and the low accessibility of the dye to some cell types. In a transgenic animal, a genetically encoded sensor could in principle be expressed specifically in any cell type and would have the advantage of staining only the cell population determined by the specificity of the promoter used to drive expression. Here we critically review the current status of these developments.
几十年前就有人设想对完整脑组织中的神经元活动进行成像,经过多年发展,电压敏感染料现在为活体大脑中神经元功能成像提供了最高的空间和时间分辨率。预计膜电位基因编码荧光传感器的新发展将推动该领域取得进一步进展。这些荧光蛋白(FP)电压传感器克服了有机电压敏感染料的缺点,如细胞染色的非特异性以及染料对某些细胞类型的低可及性。在转基因动物中,基因编码传感器原则上可以在任何细胞类型中特异性表达,并且具有仅对由用于驱动表达的启动子特异性决定的细胞群体进行染色的优势。在此,我们对这些进展的现状进行批判性综述。