Probing neuronal activities with genetically encoded optical indicators: from a historical to a forward-looking perspective

被引:13
作者
Mutoh, Hiroki [1 ]
Knoepfel, Thomas [1 ]
机构
[1] RIKEN Brain Sci Inst, Wako, Saitama 3510198, Japan
来源
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY | 2013年 / 465卷 / 03期
基金
美国国家卫生研究院;
关键词
Optical imaging; Genetically encoded indicators; Calcium; Membrane potential; INTRACELLULAR CALCIUM-CONCENTRATION; ACTIVITY-INDUCED ELEVATIONS; FLUORESCENT VOLTAGE SENSOR; SYNAPTIC-TRANSMISSION; CA2+ INDICATORS; NEURAL ACTIVITY; CONFORMATIONAL-CHANGES; LIVING CELLS; FRET; EXPRESSION;
D O I
10.1007/s00424-012-1202-z
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Optical imaging has a long history in physiology and in neurophysiology in particular. Over the past 15 years or so, new methodologies have emerged that combine genetic engineering with light-based imaging methods. This merger has resulted in a tool box of genetically encoded optical indicators that enable nondestructive and long-lasting monitoring of neuronal activities at the cellular, circuit, and system level. This review describes the historical roots and fundamental concepts underlying these new approaches, evaluates current progress in this field, and concludes with a forward-looking perspective on current work and potential future developments in this field.
引用
收藏
页码:361 / 371
页数:11
相关论文
共 90 条
[1]   Two-photon scanning microscopy of in vivo sensory responses of cortical neurons genetically encoded with fluorescent voltage sensor in rat [J].
Ahrens, Kurt F. ;
Heider, Barbara ;
Lee, Hanson ;
Isacoff, Ehud Y. ;
Siegel, RalphM. .
FRONTIERS IN NEURAL CIRCUITS, 2012, 6
[2]  
Akemann W, 2012, J NEUROPHYSIOL
[3]  
Akemann W, 2010, NAT METHODS, V7, P643, DOI [10.1038/NMETH.1479, 10.1038/nmeth.1479]
[4]   Effect of Voltage Sensitive Fluorescent Proteins on Neuronal Excitability [J].
Akemann, Walther ;
Lundby, Alicia ;
Mutoh, Hiroki ;
Knopfel, Thomas .
BIOPHYSICAL JOURNAL, 2009, 96 (10) :3959-3976
[5]   A genetically targetable fluorescent probe of channel gating with rapid kinetics [J].
Ataka, K ;
Pieribone, VA .
BIOPHYSICAL JOURNAL, 2002, 82 (01) :509-516
[6]   Circular permutation and receptor insertion within green fluorescent proteins [J].
Baird, GS ;
Zacharias, DA ;
Tsien, RY .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (20) :11241-11246
[7]   Three fluorescent protein voltage sensors exhibit low plasma membrane expression in mammalian cells [J].
Baker, B. J. ;
Lee, H. ;
Pieribone, V. A. ;
Cohen, L. B. ;
Isacoff, E. Y. ;
Knopfel, T. ;
Kosmidis, E. K. .
JOURNAL OF NEUROSCIENCE METHODS, 2007, 161 (01) :32-38
[8]   Genetically encoded fluorescent sensors of membrane potential [J].
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. ;
Knopfel, T. .
BRAIN CELL BIOLOGY, 2008, 36 (1-4) :53-67
[9]   Genetically encoded fluorescent voltage sensors using the voltage-sensing domain of Nematostella and Danio phosphatases exhibit fast kinetics [J].
Baker, Bradley J. ;
Jin, Lei ;
Han, Zhou ;
Cohen, Lawrence B. ;
Popovic, Marko ;
Platisa, Jelena ;
Pieribone, Vincent .
JOURNAL OF NEUROSCIENCE METHODS, 2012, 208 (02) :190-196
[10]   In vivo imaging of neuronal activity - Neurotechnique by targeted expression of a genetically encoded probe in the mouse [J].
Bozza, T ;
McGann, JP ;
Mombaerts, P ;
Wachowiak, M .
NEURON, 2004, 42 (01) :9-21