Optical imaging and control of genetically designated neurons in functioning circuits

被引:97
作者
Miesenböck, G
Kevrekidis, IG
机构
[1] Yale Univ, Sch Med, Dept Cell Biol, New Haven, CT 06520 USA
[2] Princeton Univ, Dept Chem Engn, Princeton, NJ 08544 USA
[3] Princeton Univ, Dept Math, Princeton, NJ 08544 USA
[4] Princeton Univ, Program Appl & Computat Math, Princeton, NJ 08544 USA
关键词
D O I
10.1146/annurev.neuro.28.051804.101610
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Proteins with engineered sensitivities to light are infiltrating the biological mechanisms by which neurons generate and detect electrochemical signals. Encoded in DNA and active only in genetically specified target cells, these proteins provide selective optical interfaces for observing and controlling signaling by defined groups of neurons in functioning circuits, in vitro and in vivo. Light-emitting sensors of neuronal activity (reporting calcium increase, neurotransmitter release, or membrane depolarization) have begun to reveal how information is represented by neuronal assemblies, and how these representations are transformed during the computations that inform behavior. Light-driven actuators control the electrical activities of central neurons in freely moving animals and establish causal connections between the activation of specific neurons and the expression of particular behaviors. Anchored within mathematical systems and control theory, the combination of finely resolved optical field sensing and finely resolved optical field actuation will open new dimensions for the analysis of the connectivity, dynamics, and plasticity of neuronal circuits, and perhaps even for replacing lost-or designing novel-functionalities.
引用
收藏
页码:533 / 563
页数:31
相关论文
共 170 条
[91]   Dynamic and quantitative Ca2+ measurements using improved cameleons [J].
Miyawaki, A ;
Griesbeck, O ;
Heim, R ;
Tsien, RY .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (05) :2135-2140
[92]   Fluorescent indicators for Ca2+ based on green fluorescent proteins and calmodulin [J].
Miyawaki, A ;
Llopis, J ;
Heim, R ;
McCaffery, JM ;
Adams, JA ;
Ikura, M ;
Tsien, RY .
NATURE, 1997, 388 (6645) :882-887
[93]   Coherent scattering in multi-harmonic light microscopy [J].
Moreaux, L ;
Sandre, O ;
Charpak, S ;
Blanchard-Desce, M ;
Mertz, J .
BIOPHYSICAL JOURNAL, 2001, 80 (03) :1568-1574
[94]   Membrane imaging by second-harmonic generation microscopy [J].
Moreaux, L ;
Sandre, O ;
Mertz, J .
JOURNAL OF THE OPTICAL SOCIETY OF AMERICA B-OPTICAL PHYSICS, 2000, 17 (10) :1685-1694
[95]   MAPPING PATTERNS OF C-FOS EXPRESSION IN THE CENTRAL-NERVOUS-SYSTEM AFTER SEIZURE [J].
MORGAN, JI ;
COHEN, DR ;
HEMPSTEAD, JL ;
CURRAN, T .
SCIENCE, 1987, 237 (4811) :192-197
[96]   STIMULUS-TRANSCRIPTION COUPLING IN THE NERVOUS-SYSTEM - INVOLVEMENT OF THE INDUCIBLE PROTOONCOGENES FOS AND JUN [J].
MORGAN, JI ;
CURRAN, T .
ANNUAL REVIEW OF NEUROSCIENCE, 1991, 14 :421-451
[97]  
NADLER B, 2005, IN PRESS APPL COMP H
[98]   Circularly permuted green fluorescent proteins engineered to sense Ca2+ [J].
Nagai, T ;
Sawano, A ;
Park, ES ;
Miyawaki, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (06) :3197-3202
[99]   Channelrhodopsin-2, a directly light-gated cation-selective membrane channel [J].
Nagel, G ;
Szellas, T ;
Huhn, W ;
Kateriya, S ;
Adeishvili, N ;
Berthold, P ;
Ollig, D ;
Hegemann, P ;
Bamberg, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (24) :13940-13945
[100]   A high signal-to-noise Ca2+ probe composed of a single green fluorescent protein [J].
Nakai, J ;
Ohkura, M ;
Imoto, K .
NATURE BIOTECHNOLOGY, 2001, 19 (02) :137-141