Publisher Correction: Temporally precise single-cell-resolution optogenetics (Nature Neuroscience (2017) DOI: 10.1038/s41593-017-0018-8);Temporally precise single-cell-resolution optogenetics

Nature Neuroscience

Volumn 20, Issue 12, 2017, Pages 1796-1806

  Shemesh, Or A ^a,b,c   Tanese, Dimitrii ^d   Zampini, Valeria ^d,e   Linghu, Changyang ^a,b,c   Piatkevich, Kiryl ^a,b,c   Ronzitti, Emiliano ^d,e   Papagiakoumou, Eirini ^d,f   Boyden, Edward S ^a,b,c   Emiliani, Valentina ^d  

^a MASSACHUSETTS INSTITUTE OF TECHNOLOGY   (United States)

^b Massachusetts Institute of Technology   (United States)

^c MASSACHUSETTS INSTITUTE OF TECHNOLOGY   (United States)

^d CNRS   (France)

^e INSTITUT DE LA VISION   (France)

^f INSERM   (France)

Author keywords

[No Author keywords available]

Indexed keywords

KAINIC ACID RECEPTOR; KINATE RECEPTOR SUBUNIT 2; OPSIN; RHODOPSIN; UNCLASSIFIED DRUG; GLUK2 KAINATE RECEPTOR;

ACCURACY; AMINO TERMINAL SEQUENCE; ANIMAL CELL; ANIMAL EXPERIMENT; ARTICLE; BRAIN CELL; BRAIN CORTEX; BRAIN SLICE; CONNECTOME; CONTROLLED STUDY; MALE; MOUSE; NONHUMAN; OPTOGENETICS; PERIKARYON; PHOTOSTIMULATION; PRIORITY JOURNAL; PROTEIN EXPRESSION; SOMATIC CELL GENETICS; ANIMAL; CYTOLOGY; DEVICES; GENETICS; NERVE CELL; NERVE CELL NETWORK; NEUROIMAGING; PATCH CLAMP TECHNIQUE; PHYSIOLOGY; PROCEDURES; THREE DIMENSIONAL IMAGING; ULTRASTRUCTURE; VISUAL CORTEX;

ANIMALS; CEREBRAL CORTEX; IMAGING, THREE-DIMENSIONAL; MICE; NERVE NET; NEUROIMAGING; NEURONS; OPSINS; OPTOGENETICS; PATCH-CLAMP TECHNIQUES; PHOTIC STIMULATION; RECEPTORS, KAINIC ACID; VISUAL CORTEX;

EID: 85032807479     PISSN: 10976256     EISSN: 15461726     Source Type: Journal    
DOI: 10.1038/s41593-018-0097-1     Document Type: Erratum

References (61)

1. Boyden, E. S. A history of optogenetics: the development of tools for controlling brain circuits with light. F1000 Biol. Repc. 3, 11 (2011).
2. Dombeck, D. A., Harvey, C. D., Tian, L., Looger, L. L. & Tank, D. W. Functional imaging of hippocampal place cells at cellular resolution during virtual navigation. Nat. Neurosci. 13, 1433-1440 (2010).
3. Li, C.-Y. T., Poo, M.-M. & Dan, Y. Burst spiking of a single cortical neuron modifies global brain state. Science 324, 643-646 (2009).
4. Houweling, A. R. & Brecht, M. Behavioural report of single neuron stimulation in somatosensory cortex. Nature 451, 65-68 (2008).
5. Rickgauer, J. P. & Tank, D. W. Two-photon excitation of channelrhodopsin-2 at saturation. Proc. Natl. Acad. Sci. USA 106, 15025-15030 (2009).
6. Ronzitti, E. et al. Recent advances in patterned photostimulation for optogenetics, J. Opt. 19, 113001 (2017).
7. Papagiakoumou, E. et al. Scanless two-photon excitation of channelrhodopsin-2. Nat. Methods 7, 848-854 (2010).
8. Papagiakoumou, E., de Sars, V., Oron, D. & Emiliani, V. Patterned two-photon illumination by spatiotemporal shaping of ultrashort pulses. Opt. Express 16, 22039-22047 (2008).
9. Bègue, A. et al. Two-photon excitation in scattering media by spatiotemporally shaped beams and their application in optogenetic stimulation. Biomed. Opt. Express 4, 2869-2879 (2013).
10. Chaigneau, E. et al. Two-photon holographic stimulation of ReaChR. Front. Cell. Neurosci. 10, 234 (2016).
11. Ronzitti, E. et al. Sub-millisecond optogenetic control of neuronal firing with two-photon holographic photoactivation of Chronos. J. Neurosci. https://doi.org/10.1523/JNEUROSCI.1246-17.2017 (2017).
12. Hernandez, O. et al. Three-dimensional spatiotemporal focusing of holographic patterns. Nat. Commun. 7, 11928 (2016).
13. Papagiakoumou, E. et al. Functional patterned multiphoton excitation deep inside scattering tissue. Nat. Photonics 7, 274-278 (2013).
14. Packer, A. M. et al. Two-photon optogenetics of dendritic spines and neural circuits. Nat. Methods 9, 1202-1205 (2012).
15. Anselmi, F., Ventalon, C., Bègue, A., Ogden, D. & Emiliani, V. Three-dimensional imaging and photostimulation by remote-focusing and holographic light patterning. Proc. Natl. Acad. Sci. USA 108, 19504-19509 (2011).
16. Dal Maschio, M., Donovan, J. C., Helmbrecht, T. O. & Baier, H. Linking neurons to network function and behavior by two-photon holographic optogenetics and volumetric imaging. Neuron 94, 774-789.e5 (2017).
17. Nicholson, C. & Syková, E. Extracellular space structure revealed by diffusion analysis. Trends Neurosci. 21, 207-215 (1998).
18. Valluru, L. et al. Ligand binding is a critical requirement for plasma membrane expression of heteromeric kainate receptors. J. Biol. Chem. 280, 6085-6093 (2005).
19. Klapoetke, N. C. et al. Independent optical excitation of distinct neural populations. Nat. Methods 11, 338-346 (2014).
20. Jacobs, E. C., Bongarzone, E. R., Campagnoni, C. W., Kampf, K. & Campagnoni, A. T. Soma-restricted products of the myelin proteolipid gene are expressed primarily in neurons in the developing mouse nervous system. Dev. Neurosci. 25, 96-104 (2003).
21. + channel in hippocampal neurons. Neuron 25, 385-397 (2000).
22. Garrido, J. J. et al. A targeting motif involved in sodium channel clustering at the axonal initial segment. Science 300, 2091-2094 (2003).
23. Schäfer, M. K. E. et al. L1 syndrome mutations impair neuronal L1 function at different levels by divergent mechanisms. Neurobiol. Dis. 40, 222-237 (2010).
24. Bianco, A., Dienstbier, M., Salter, H. K., Gatto, G. & Bullock, S. L. Bicaudal-D regulates fragile X mental retardation protein levels, motility, and function during neuronal morphogenesis. Curr. Biol. 20, 1487-1492 (2010).
25. Ran, B., Bopp, R. & Suter, B. Null alleles reveal novel requirements for Bic-D during Drosophila oogenesis and zygotic development. Development 120, 1233-1242 (1994).
26. Zhang, X. & Bennett, V. Restriction of 480/270-kD ankyrin G to axon proximal segments requires multiple ankyrin G-specific domains. J. Cell Biol. 142, 1571-1581 (1998).
27. Wu, C., Ivanova, E., Zhang, Y. & Pan, Z.-H. rAAV-mediated subcellular targeting of optogenetic tools in retinal ganglion cells in vivo. PLoS One 8, e66332 (2013).
28. Greenberg, K. P., Pham, A. & Werblin, F. S. Differential targeting of optical neuromodulators to ganglion cell soma and dendrites allows dynamic control of center-surround antagonism. Neuron 69, 713-720 (2011).
29. Marchler-Bauer, A. et al. CDD: NCBI's conserved domain database. Nucleic Acids Res. 43, D222-D226 (2015).
30. Ren, Z. et al. Multiple trafficking signals regulate kainate receptor KA2 subunit surface expression. J. Neurosci. 23, 6608-6616 (2003).
31. Grubb, M. S. & Burrone, J. Channelrhodopsin-2 localised to the axon initial segment. PLoS One 5, e13761 (2010).
32. Zhang, Z., Feng, J., Wu, C., Lu, Q. & Pan, Z.-H. Targeted expression of channelrhodopsin-2 to the axon initial segment alters the temporal firing properties of retinal ganglion cells. PLoS One 10, e0142052 (2015).
33. Baker, C. A., Elyada, Y. M., Parra, A. & Bolton, M. M. Cellular resolution circuit mapping with temporal-focused excitation of soma-targeted channelrhodopsin. Elife 5, e14193 (2016).
34. Helmchen, F. & Denk, W. Deep tissue two-photon microscopy. Nat. Methods 2, 932-940 (2005).
35. Szabo, V., Ventalon, C., De Sars, V., Bradley, J. & Emiliani, V. Spatially selective holographic photoactivation and functional fluorescence imaging in freely behaving mice with a fiberscope. Neuron 84, 1157-1169 (2014).
36. Brill, J., Mattis, J., Deisseroth, K. & Huguenard, J. R. LSPS/optogenetics to improve synaptic connectivity mapping: unmasking the role of basket cell-mediated feedforward inhibition. eNeuro 3, ENEURO.0142-15.2016 (2016).
37. Kohara, K. et al. Cell type-specific genetic and optogenetic tools reveal hippocampal CA2 circuits. Nat. Neurosci. 17, 269-279 (2014).
38. Little, J. P. & Carter, A. G. Subcellular synaptic connectivity of layer 2 pyramidal neurons in the medial prefrontal cortex. J. Neurosci. 32, 12808-12819 (2012).
39. Pala, A. & Petersen, C. C. In vivo measurement of cell-type-specific synaptic connectivity and synaptic transmission in layer 2/3 mouse barrel cortex. Neuron 85, 68-75 (2015).
40. Liu, X. et al. Optogenetic stimulation of a hippocampal engram activates fear memory recall. Nature 484, 381-385 (2012).
41. Xu, C. & Webb, W. W. Measurement of two-photon excitation cross sections of molecular fluorophores with data from 690 to 1050 nm. J. Opt. Soc. Am. B 13, 481 (1996).
42. Chuong, A. S. et al. Noninvasive optical inhibition with a red-shifted microbial rhodopsin. Nat. Neurosci. 17, 1123-1129 (2014).
43. Song, S., Sjöström, P. J., Reigl, M., Nelson, S. & Chklovskii, D. B. Highly nonrandom features of synaptic connectivity in local cortical circuits. PLoS Biol. 3, e68 (2005).
44. Yoshimura, Y., Dantzker, J. L. M. & Callaway, E. M. Excitatory cortical neurons form fine-scale functional networks. Nature 433, 868-873 (2005).
45. Ikegaya, Y. et al. Synfire chains and cortical songs: temporal modules of cortical activity. Science 304, 559-564 (2004).
46. Petreanu, L., Huber, D., Sobczyk, A. & Svoboda, K. Channelrhodopsin-2-assisted circuit mapping of long-range callosal projections. Nat. Neurosci. 10, 663-668 (2007).
47. 2+-phosphate transfection efficiency in low-density neuronal cultures. Nat. Protoc. 1, 695-700 (2006).
48. Chow, B. Y. et al. High-performance genetically targetable optical neural silencing by light-driven proton pumps. Nature 463, 98-102 (2010).
49. Ma, D. et al. Role of ER export signals in controlling surface potassium channel numbers. Science 291, 316-319 (2001).
50. Hofherr, A., Fakler, B. & Klöcker, N. Selective Golgi export of Kir2.1 controls the stoichiometry of functional Kir2.x channel heteromers. J. Cell Sci. 118, 1935-1943 (2005).
51. Ducros, M. et al. Efficient large core fiber-based detection for multi-channel two-photon fluorescence microscopy and spectral unmixing. J. Neurosci. Methods 198, 172-180 (2011).
52. Lutz, C. et al. Holographic photolysis of caged neurotransmitters. Nat. Methods 5, 821-827 (2008).
53. Gerchberg, R. & Saxton, W. A practical algorithm for the determination of the phase from image and diffraction plane pictures. Optik 35, 237 (1972).
54. Haist, T., Schönleber, M. & Tiziani, H. J. Computer-generated holograms from 3D-objects written on twisted-nematic liquid crystal displays. Opt. Commun. 140, 299-308 (1997).
55. Hernandez, O., Guillon, M., Papagiakoumou, E. & Emiliani, V. Zero-order suppression for two-photon holographic excitation. Opt. Lett. 39, 5953-5956 (2014).
56. Golan, L., Reutsky, I., Farah, N. & Shoham, S. Design and characteristics of holographic neural photo-stimulation systems. J. Neural Eng. 6, 066004 (2009).
57. Yang, S. et al. Three-dimensional holographic photostimulation of the dendritic arbor. J. Neural Eng. 8, 046002 (2011).
58. Conti, R., Assayag, O., de Sars, V., Guillon, M. & Emiliani, V. Computer generated holography with intensity-graded patterns. Front. Cell. Neurosci. 10, 236 (2016).
59. Mütze, J. et al. Excitation spectra and brightness optimization of two-photon excited probes. Biophys. J. 102, 934-944 (2012).
60. Horton, N. G. et al. In vivo three-photon microscopy of subcortical structures within an intact mouse brain. Nat. Photonics 7, 205-209 (2013).
61. Dell, R. B., Holleran, S. & Ramakrishnan, R. Sample size determination. ILAR J. 43, 207-213 (2002).