Spatially asymmetric reorganization of inhibition establishes a motion-sensitive circuit

Nature

Volumn 469, Issue 7330, 2011, Pages 407-410

  Yonehara, Keisuke ^a   Balint, Kamill ^a   Noda, Masaharu ^b,c   Nagel, Georg ^d   Bamberg, Ernst ^e,f   Roska, Botond ^a  

^a FRIEDRICH MIESCHER INSTITUTE FOR BIOMEDICAL RESEARCH   (Switzerland)

^b NATIONAL INSTITUTE FOR BASIC BIOLOGY   (Japan)

^c GRADUATE UNIVERSITY FOR ADVANCED STUDIES   (Japan)

^d UNIVERSITY OF WÜRZBURG   (Germany)

^e MAX PLANCK INSTITUTE OF BIOPHYSICS   (Germany)

^f GOETHE UNIVERSITY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

CELL ORGANELLE; INHIBITION; NEUROLOGY; SPATIAL DISTRIBUTION;

ANIMAL CELL; ARTICLE; CELL LABELING; DIRECTIONALLY SELECTIVE RETINAL GANGLION CELL; MOUSE; NERVE CELL STIMULATION; NONHUMAN; PHOTOSTIMULATION; PRIORITY JOURNAL; RETINA GANGLION CELL; SIGNAL TRANSDUCTION; SPATIAL DISCRIMINATION; SYNAPTIC POTENTIAL; SYNAPTIC TRANSMISSION;

ACTION POTENTIALS; AMACRINE CELLS; ANIMALS; FEMALE; LIGHT; MALE; MICE; MODELS, NEUROLOGICAL; MOTION; MOTION PERCEPTION; NEURAL INHIBITION; NEURAL PATHWAYS; NEUROANATOMICAL TRACT-TRACING TECHNIQUES; PHOTIC STIMULATION; RABIES VIRUS; RETINA; RETINAL GANGLION CELLS; RHODOPSIN; SYNAPSES;

EID: 78751645478     PISSN: 00280836     EISSN: 14764687     Source Type: Journal    
DOI: 10.1038/nature09711     Document Type: Article

References (34)

1. Hubel, D. H. & Wiesel, T. N. Receptive fields, Binocular interaction and functional architecture in the cat's visual cortex. J. Physiol. (Lond.) 160, 106-154 (1962).
2. Barlow, H. B. & Hill, R. M. Selective sensitivity to direction ofmovement in ganglion cells of the rabbit retina. Science 139, 412-414 (1963).
3. Fried, S. I., Munch, T. A. & Werblin, F. S. Mechanisms and circuitry underlying directional selectivity in the retina. Nature 420, 411-414 (2002).
4. Euler, T., Detwiler, P. B. & Denk, W. Directionally selective calcium signals in dendrites of starburst amacrine cells. Nature 418, 845-852 (2002).
5. Lee, S. & Zhou, Z. J. The synaptic mechanism of direction selectivity in distal processes of starburst amacrine cells. Neuron 51, 787-799 (2006).
6. Bamann, C., Gueta, R., Kleinlogel, S., Nagel, G. & Bamberg, E. Structural guidance of the photocycle of channelrhodopsin-2 by an interhelical hydrogen bond. Biochemistry 49, 267-278 (2010).
7. Berndt, A., Yizhar, O., Gunaydin, L. A., Hegemann, P. & Deisseroth, K. Bi-stable neural state switches. Nature Neurosci. 12, 229-234 (2008).
8. Radu, I. et al. Conformational changes of channelrhodopsin-2. J. Am. Chem. Soc. 131, 7313-7319 (2009).
9. Yonehara, K. et al. Identification of retinal ganglion cells and their projections involved in central transmission of information about upward and downward image motion. PLoS ONE 4, E4320 (2009).
10. Yonehara, K. et al. Expression of SPIG1 reveals development of a retinal ganglion cell subtype projecting to the medial terminal nucleus in the mouse. PLoS ONE 3, E1533 (2008).
11. Vaney, D. I. & Taylor, W. R. Direction selectivity in the retina. Curr. Opin. Neurobiol. 12, 405-410 (2002).
12. Barlow, H. B. & Levick, W. R. The mechanism of directionally selective units in rabbit's retina. J. Physiol. (Lond.) 178, 477-504 (1965).
13. Demb, J. B. Cellular mechanisms for direction selectivity in the retina. Neuron 55, 179-186 (2007).
14. Fried, S. I., Munch, T. A. & Werblin, F. S. Directional selectivity is formed at multiple levels by laterally offset inhibition in the rabbit retina.Neuron 46, 117-127 (2005).
15. Ariel, M. & Daw, N. W. Pharmacological analysis of directionally sensitive rabbit retinal ganglion cells. J. Physiol. (Lond.) 324, 161-185 (1982). (Pubitemid 12132468)
16. Masland, R. H. & Ames, A. III. Responses to acetylcholine of ganglion cells in an isolated mammalian retina. J. Neurophysiol. 39, 1220-1235 (1976).
17. Chan, Y. C. & Chiao, C. C. Effect of visual experience on the maturation of ON-OFF direction selective ganglion cells in the rabbit retina. Vision Res. 48, 2466-2475 (2008).
18. Chen, M., Weng, S., Deng, Q., Xu, Z. & He, S. Physiological properties of directionselective ganglion cells in early postnatal and adultmouse retina. J. Physiol. (Lond.) 587, 819-828 (2009).
19. Elstrott, J. et al. Direction selectivity in the retina is established independent of visual experience and cholinergic retinal waves. Neuron 58, 499-506 (2008).
20. Tian, N. & Copenhagen, D. R. Visual deprivation alters development of synaptic function in inner retina after eye opening. Neuron 32, 439-449 (2001).
21. Hattar, S., Liao, H. W., Takao, M., Berson, D. M. & Yau, K. W. Melanopsin-containing retinal ganglion cells: architecture, Projections, And intrinsic photosensitivity. Science 295, 1065-1070 (2002).
22. Oyster, C. W., Takahashi, E. & Collewijn, H. Direction-selective retinal ganglion cells and control of optokinetic nystagmus in the rabbit. Vision Res. 12, 183-193 (1972).
23. Simpson, J. I. The accessory optic system. Annu. Rev. Neurosci. 7, 13-41 (1984).
24. Sun, W., Deng, Q., Levick, W. R. & He, S. ON direction-selective ganglion cells in the mouse retina. J. Physiol. (Lond.) 576, 197-202 (2006).
25. Ivanova, E., Hwang, G. S. & Pan, Z. H. Characterization of transgenic mouse lines expressing Cre recombinase in the retina. Neuroscience 165, 233-243 (2010).
26. Tang, W. et al. Faithful expression of multiple proteins via 2A-peptide selfprocessing: a versatile and reliable method for manipulating brain circuits. J. Neurosci. 29, 8621-8629 (2009).
27. Wickersham, I. R. et al. Monosynaptic restriction of transsynaptic tracing from single, Genetically targeted neurons. Neuron 53, 639-647 (2007).
28. Stepien, A. E., Tripodi, M. & Arber, S. Monosynaptic rabies virus reveals premotor network organization and synaptic specificity of cholinergic partition cells. Neuron 68, 456-472 (2010).
29. Roska, B. & Werblin, F. Vertical interactions across ten parallel, Stacked representations in the mammalian retina. Nature 410, 583-587 (2001). (Pubitemid 32267202)
30. Münch, T. A. et al. Approach sensitivity in the retina processed by amultifunctional neural circuit. Nature Neurosci. 12, 1308-1316 (2009).
31. Atasoy, D., Aponte, Y., Su, H. H. & Sternson, S. M. A. FLEX switch targets channelrhodopsin-2 to multiple cell types for imaging and long-range circuit mapping. J. Neurosci. 28, 7025-7030 (2008).
32. Trichas, G., Begbie, J. & Srinivas, S. Use of the viral 2A peptide for bicistronic expression in transgenic mice. BMC Biol. 6, 40 (2008).
33. Sena-Esteves, M., Tebbets, J. C., Steffens, S., Crombleholme, T. & Flake, A. W. Optimized large-scale production of high titer lentivirus vector pseudotypes. J. Virol. Methods 122, 131-139 (2004).
34. Marshel, J. H., Mori, T., Nielsen, K. J. & Callaway, E. M. Targeting single neuronal networks for gene expressionand cell labeling in vivo. Neuron 67, 562-574 (2010).