Genetically encoded fluorescent sensors of membrane potential

被引:72
作者
Baker, B. J. [2 ]
Mutoh, H. [1 ]
Dimitrov, D. [1 ]
Akemann, W. [1 ]
Perron, A. [1 ]
Iwamoto, Y. [1 ]
Jin, L. [2 ]
Cohen, L. B. [2 ]
Isacoff, E. Y. [3 ]
Pieribone, V. A. [2 ,4 ]
Hughes, T. [5 ]
Knopfel, T. [1 ]
机构
[1] RIKEN, Brain Sci Inst, Lab Neuronal Circuit Dynam, Wako, Saitama 3510198, Japan
[2] Yale Univ, Sch Med, Dept Cellular & Mol Physiol, New Haven, CT 06520 USA
[3] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
[4] John B Pierce Lab, New Haven, CT 06520 USA
[5] Montana State Univ, Dept Cell Biol & Neurosci, Bozeman, MT 59717 USA
关键词
D O I
10.1007/s11068-008-9026-7
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
引用
收藏
页码:53 / 67
页数:15
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