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2017 | OriginalPaper | Chapter

9. Implantable Optical Neural Interface

Authors : Sang Beom Jun, Yoonseob Lim

Published in: Smart Sensors and Systems

Publisher: Springer International Publishing

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Abstract

For more than several decades, due to the rapid development of sophisticated electronics, the electrical neural interface has become the most popular method for recording and modulating neural activity in nerve systems. The electrical neural interface has been successfully applied to implantable neural prosthetic systems such as cochlear implant, deep brain stimulation system, artificial retina, and so on. Recently, in order to overcome the limitations of electrical methods for neural interface, novel optical technologies have been developed and applied to neuroscience research. Overall, the optical neural interfaces can be categorized into the intrinsic and the extrinsic methods depending on the modification of natural nerve system. For example, infrared neural stimulation (INS) and optogenetic neural stimulation are the typical methods for intrinsic and extrinsic neural interfaces, respectively. In addition to the optogenetic stimulation, it is also possible to monitor neural activity from specific neurons genetically modified to express activity-correlated fluorescence signals. Therefore, the optogenetic neural recording enables the detection of activity from specific types of neurons. Despite the fascinating advantages, to date, the use of the optical neural interface is limited only to the neuroscience research not for clinical purposes. In this chapter, the state-of-art technologies in optical neural interface are reviewed from the aspects of both neurobiology and engineering. In addition, the challenges to realize the clinical use of optical neural interfaces are discussed.

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Shepherd GM (2004) The synaptic organization of the brain, 5th edn. Oxford University Press, New YorkCrossRef

Pinaud R, Terleph TA, Tremere LA, Phan ML, Dagostin AA, Leão RM et al (2008) Inhibitory network interactions shape the auditory processing of natural communication signals in the songbird auditory forebrain. J Neurophysiol 100:441–455CrossRef

Zhou M, Liang F, Xiong XR, Li L, Li H, Xiao Z et al (2014) Scaling down of balanced excitation and inhibition by active behavioral states in auditory cortex. Nat Neurosci 17:841–850

Pinto L, Dan Y (2015) Cell-type-specific activity in prefrontal cortex during goal-directed behavior. Neuron 87:437–450

Roche JP, Hansen MR (2015) On the horizon: cochlear implant technology. Otolaryngol Clin North Am 48:1097–1116CrossRef

Kilgard MP, Merzenich MM (1998) Cortical map reorganization enabled by nucleus basalis activity. Science 279:1714–1718CrossRef

Zrenner E (2002) Will retinal implants restore vision? Science 295:1022–1025

Zhang Y, Hakes JJ, Bonfield SP, Yan J (2005) Corticofugal feedback for auditory midbrain plasticity elicited by tones and electrical stimulation of basal forebrain in mice. Eur J Neurosci 22:871–879CrossRef

Lim H, Anderson D (2006) Auditory cortical responses to electrical stimulation of the inferior colliculus: implications for an auditory midbrain implant. J Neurophysiol 96:975–988CrossRef

10.

Thompson AC, Stoddart PR, Jansen ED (2014) Optical stimulation of neurons. Curr Mol Imaging 3:162–177CrossRef

11.

Frostig RD, Lieke EE, Ts’o DY, Grinvald A (1990) Cortical functional architecture and local coupling between neuronal activity and the microcirculation revealed by in vivo high-resolution optical imaging of intrinsic signals. Proc Natl Acad Sci 87:6082–6086CrossRef

12.

Malonek D, Grinvald A (1996) Interactions between electrical activity and cortical microcirculation revealed by imaging spectroscopy: implications for functional brain mapping. Science 272:551CrossRef

13.

Kim SA, Byun KM, Lee J, Kim J, Kim D-G, Baac H et al (2008) Optical measurement of neural activity using surface plasmon resonance. Opt Lett 33:914–916CrossRef

14.

Kim SA, Kim SJ, Moon H, Jun SB (2012) In vivo optical neural recording using fiber-based surface plasmon resonance. Opt Lett 37:614–616CrossRef

15.

Lazebnik M, Marks DL, Potgieter K, Gillette R, Boppart SA (2003) Functional optical coherence tomography for detecting neural activity through scattering changes. Opt Lett 28:1218–1220CrossRef

16.

Stepnoski R, LaPorta A, Raccuia-Behling F, Blonder G, Slusher R, Kleinfeld D (1991) Noninvasive detection of changes in membrane potential in cultured neurons by light scattering. Proc Natl Acad Sci 88:9382–9386CrossRef

17.

Shevelev IA (1998) Functional imaging of the brain by infrared radiation (thermoencephaloscopy). Prog Neurobiol 56:269–305CrossRef

18.

Wells J, Kao C, Jansen ED, Konrad P, Mahadevan-Jansen A (2005) Application of infrared light for in vivo neural stimulation. J Biomed Opt 10:064003CrossRef

19.

Tan X, Rajguru S, Young H, Xia N, Stock SR, Xiao X et al (2015) Radiant energy required for infrared neural stimulation. Sci Rep 5:13273CrossRef

20.

Wells J, Konrad P, Kao C, Jansen ED, Mahadevan-Jansen A (2007) Pulsed laser versus electrical energy for peripheral nerve stimulation. J Neurosci Methods 163:326–337CrossRef

21.

Izzo AD, Walsh JT Jr, Ralph H, Webb J, Bendett M, Wells J et al (2008) Laser stimulation of auditory neurons: effect of shorter pulse duration and penetration depth. Biophys J 94:3159–3166CrossRef

22.

Huang H, Delikanli S, Zeng H, Ferkey DM, Pralle A (2010) Remote control of ion channels and neurons through magnetic-field heating of nanoparticles. Nat Nanotechnol 5:602–606CrossRef

23.

Richter CP, Matic AI, Wells JD, Jansen ED, Walsh JT Jr (2011) Neural stimulation with optical radiation. Laser Photonics Rev 5:68–80CrossRef

24.

Shapiro MG, Homma K, Villarreal S, Richter CP, Bezanilla F (2012) Infrared light excites cells by changing their electrical capacitance. Nat Commun 3:736CrossRef

25.

Wells J, Kao C, Konrad P, Milner T, Kim J, Mahadevan-Jansen A et al (2007) Biophysical mechanisms of transient optical stimulation of peripheral nerve. Biophys J 93:2567–2580CrossRef

26.

Duke AR, Jenkins MW, Lu H, McManus JM, Chiel HJ, Jansen ED (2013) Transient and selective suppression of neural activity with infrared light. Sci Rep 3:2600CrossRef

27.

Katz EJ, Ilev IK, Krauthamer V, Kim do H, Weinreich D (2010) Excitation of primary afferent neurons by near-infrared light in vitro. Neuroreport 21:662–666CrossRef

28.

Jaque D, Martinez Maestro L, del Rosal B, Haro-Gonzalez P, Benayas A, Plaza JL et al (2014) Nanoparticles for photothermal therapies. Nanoscale 6:9494–9530CrossRef

29.

Carvalho-de-Souza JL, Treger JS, Dang B, Kent SB, Pepperberg DR, Bezanilla F (2015) Photosensitivity of neurons enabled by cell-targeted gold nanoparticles. Neuron 86:207–217CrossRef

30.

Eom K, Kim J, Choi JM, Kang T, Chang JW, Byun KM et al (2014) Enhanced infrared neural stimulation using localized surface plasmon resonance of gold nanorods. Small 10:3853–3857CrossRef

31.

Yong J, Needham K, Brown WG, Nayagam BA, McArthur SL, Yu A et al (2014) Gold-nanorod-assisted near-infrared stimulation of primary auditory neurons. Adv Healthc Mater 3:1862–1868CrossRef

32.

Yoo S, Hong S, Choi Y, Park JH, Nam Y (2014) Photothermal inhibition of neural activity with near-infrared-sensitive nanotransducers. ACS Nano 8:8040–8049CrossRef

33.

Barnard JE, Welch FV (1936) Fluorescence microscopy with high powers. J R Microsc Soc 56:361–364CrossRef

34.

Abramowitz M (1993) Fluorescence microscopy. Olympus America, New York

35.

Shimomura O, Johnson FH, Saiga Y (1962) Extraction, purification and properties of aequorin, a bioluminescent protein from the luminous hydromedusan, aequorea. J Cell Comp Physiol 59:223–239CrossRef

36.

Helmchen F, Denk W (2005) Deep tissue two-photon microscopy. Nat Methods 2:932–940CrossRef

37.

Kerr JND, Denk W (2008) Imaging in vivo: watching the brain in action. Nat Rev Neurosci 9:195–205CrossRef

38.

Rothschild G, Nelken I, Mizrahi A (2010) Functional organization and population dynamics in the mouse primary auditory cortex. Nat Neurosci 13:353–360CrossRef

39.

Roberts TF, Tschida KA, Klein ME, Mooney R (2010) Rapid spine stabilization and synaptic enhancement at the onset of behavioural learning. Nature 463:948–952CrossRef

40.

Clancy KB, Koralek AC, Costa RM, Feldman DE, Carmena JM (2014) Volitional modulation of optically recorded calcium signals during neuroprosthetic learning. Nat Neurosci 17:807–809CrossRef

41.

Helmchen F, Fee MS, Tank DW, Denk W (2001) A miniature head-mounted two-photon microscope. Neuron 31:903–912CrossRef

42.

Flusberg BA, Jung JC, Cocker ED, Anderson EP, Schnitzer MJ (2005) In vivo brain imaging using a portable 3.9 gram two-photon fluorescence microendoscope. Opt Lett 30:2272–2274CrossRef

43.

Sawinski J, Denk W (2007) Miniature random-access fiber scanner for in vivo multiphoton imaging. J Appl Phys 102:034701CrossRef

44.

Engelbrecht CJ, Johnston RS, Seibel EJ, Helmchen F (2008) Ultra-compact fiber-optic two-photon microscope for functional fluorescence imaging in vivo. Opt Express 16:5556–5564CrossRef

45.

Sawinski J, Wallace DJ, Greenberg DS, Grossmann S, Denk W, Kerr JND (2009) Visually evoked activity in cortical cells imaged in freely moving animals. Proc Natl Acad Sci U S A 106:19557–19562CrossRef

46.

Piyawattanametha W, Cocker ED, Burns LD, Barretto RPJ, Jung JC, Ra H et al (2009) In vivo brain imaging using a portable 2.9 g two-photon microscope based on a microelectromechanical systems scanning mirror. Opt Lett 34:2309–2311CrossRef

47.

Jung JC, Schnitzer MJ (2003) Multiphoton endoscopy. Opt Lett 28:902–904CrossRef

48.

Levene MJ, Dombeck DA, Kasischke KA, Molloy RP, Webb WW (2004) In vivo multiphoton microscopy of deep brain tissue. J Neurophysiol 91:1908–1912CrossRef

49.

Jung JC, Mehta AD, Aksay E, Stepnoski R, Schnitzer MJ (2004) In vivo mammalian brain imaging using one- and two-photon fluorescence microendoscopy. J Neurophysiol 92:3121–3133CrossRef

50.

Llewellyn ME, Barretto RPJ, Delp SL, Schnitzer MJ (2008) Minimally invasive high-speed imaging of sarcomere contractile dynamics in mice and humans. Nature 454:784–788

51.

Bocarsly ME, Jiang W-c, Wang C, Dudman JT, Ji N, Aponte Y (2015) Minimally invasive microendoscopy system for in vivo functional imaging of deep nuclei in the mouse brain. Biomed Opt Express 6:4546–4556CrossRef

52.

Grienberger C, Konnerth A (2012) Imaging calcium in neurons. Neuron 73:862–885CrossRef

53.

Cao G, Platisa J, Pieribone VA, Raccuglia D, Kunst M, Nitabach MN (2013) Genetically targeted optical electrophysiology in intact neural circuits. Cell 154:904–913CrossRef

54.

Mutoh H, Perron A, Akemann W, Iwamoto Y, Knopfel T (2010) Optogenetic monitoring of membrane potentials. Exp Physiol 96:13–18CrossRef

55.

Gonzalez D, Espino J, Bejarano I, Lopez JJ, Rodriguez AB, Pariente JA (2010) Caspase-3 and -9 are activated in human myeloid HL-60 cells by calcium signal. Mol Cell Biochem 333:151–157CrossRef

56.

Zhang H, Liu J, Sun S, Pchitskaya E, Popugaeva E, Bezprozvanny I (2015) Calcium signaling, excitability, and synaptic plasticity defects in a mouse model of Alzheimer’s disease. J Alzheimers Dis 45:561–580

57.

Lyons MR, West AE (2011) Mechanisms of specificity in neuronal activity-regulated gene transcription. Prog Neurobiol 94:259–295CrossRef

58.

Berridge MJ, Lipp P, Bootman MD (2000) The versatility and universality of calcium signalling. Nat Rev Mol Cell Biol 1:11–21CrossRef

59.

Wachowiak M, Knopfel T (2009) Frontiers in neuroscience optical imaging of brain activity in vivo using genetically encoded probes. In: Frostig RD (ed) In vivo optical imaging of brain function. CRC Press and Taylor & Francis Group, LLC, Boca Raton, FL

60.

Paredes RM, Etzler JC, Watts LT, Zheng W, Lechleiter JD (2008) Chemical calcium indicators. Methods 46:143–151CrossRef

61.

Pozzan T, Arslan P, Tsien RY, Rink TJ (1982) Anti-immunoglobulin, cytoplasmic free calcium, and capping in B lymphocytes. J Cell Biol 94:335–340CrossRef

62.

Tsien RY, Pozzan T, Rink TJ (1982) Calcium homeostasis in intact lymphocytes: cytoplasmic free calcium monitored with a new, intracellularly trapped fluorescent indicator. J Cell Biol 94:325–334CrossRef

63.

Neher E (1995) The use of fura-2 for estimating Ca buffers and Ca fluxes. Neuropharmacology 34:1423–1442CrossRef

64.

Dittgen T, Nimmerjahn A, Komai S, Licznerski P, Waters J, Margrie TW et al (2004) Lentivirus-based genetic manipulations of cortical neurons and their optical and electrophysiological monitoring in vivo. Proc Natl Acad Sci U S A 101:18206–18211CrossRef

65.

Monahan PE, Samulski RJ (2000) Adeno-associated virus vectors for gene therapy: more pros than cons? Mol Med Today 6:433–440CrossRef

66.

Wirth D, Gama-Norton L, Riemer P, Sandhu U, Schucht R, Hauser H (2007) Road to precision: recombinase-based targeting technologies for genome engineering. Curr Opin Biotechnol 18:411–419CrossRef

67.

Tsai PS, Friedman B, Ifarraguerri AI, Thompson BD, Lev-Ram V, Schaffer CB et al (2003) All-optical histology using ultrashort laser pulses. Neuron 39:27–41CrossRef

68.

Chemla S, Chavane F (2010) Voltage-sensitive dye imaging: technique review and models. J Physiol Paris 104:40–50CrossRef

69.

Siegel MS, Isacoff EY (1997) A genetically encoded optical probe of membrane voltage. Neuron 19:735–741CrossRef

70.

Akemann W, Mutoh H, Perron A, Rossier J, Knöpfel T (2010) Imaging brain electric signals with genetically targeted voltage-sensitive fluorescent proteins. Nat Methods 7:643–649CrossRef

71.

Akemann W, Sasaki M, Mutoh H, Imamura T, Honkura N, Knöpfel T (2013) Two-photon voltage imaging using a genetically encoded voltage indicator. Sci Rep 3:2231CrossRef

72.

Ross WN, Werman R (1987) Mapping calcium transients in the dendrites of Purkinje cells from the guinea-pig cerebellum in vitro. J Physiol 389:319–336CrossRef

73.

Baker BJ, Kosmidis EK, Vucinic D, Falk CX, Cohen LB, Djurisic M et al (2005) Imaging brain activity with voltage- and calcium-sensitive dyes. Cell Mol Neurobiol 25:245–282CrossRef

74.

Adelsberger H, Garaschuk O, Konnerth A (2005) Cortical calcium waves in resting newborn mice. Nat Neurosci 8:988–990CrossRef

75.

Cui G, Jun SB, Jin X, Pham MD, Vogel SS, Lovinger DM et al (2013) Concurrent activation of striatal direct and indirect pathways during action initiation. Nature 494:238–242CrossRef

76.

Minsky M (1988) Memoir on inventing the confocal scanning microscope. Scanning 10:128–138CrossRef

77.

Pawley JB (ed) (2006) Handbook of biological confocal microscopy. Springer, Boston, MA

78.

Denk W, Strickler J, Webb WW (1990) Two-photon laser scanning fluorescence microscopy. Science 248:73–76CrossRef

79.

Kobat D, Horton NG, Xu C (2011) In vivo two-photon microscopy to 1.6-mm depth in mouse cortex. J Biomed Opt 16:106014CrossRef

80.

Horton NG, Wang K, Kobat D, Clark CG, Wise FW, Schaffer CB et al (2013) In vivo three-photon microscopy of subcortical structures within an intact mouse brain. Nat Photonics 7:205–209CrossRef

81.

Flusberg BA, Nimmerjahn A, Cocker ED, Mukamel EA, Barretto RPJ, Ko TH et al (2008) High-speed, miniaturized fluorescence microscopy in freely moving mice. Nat Methods 5:935–938CrossRef

82.

Barretto RPJ, Messerschmidt B, Schnitzer MJ (2009) In vivo fluorescence imaging with high-resolution microlenses. Nat Methods 6:511–512CrossRef

83.

Zemelman BV, Lee GA, Ng M, Miesenbock G (2002) Selective photostimulation of genetically chARGed neurons. Neuron 33:15–22CrossRef

84.

Zemelman BV, Nesnas N, Lee GA, Miesenbock G (2003) Photochemical gating of heterologous ion channels: remote control over genetically designated populations of neurons. Proc Natl Acad Sci U S A 100:1352–1357CrossRef

85.

Lima SQ, Miesenbock G (2005) Remote control of behavior through genetically targeted photostimulation of neurons. Cell 121:141–152CrossRef

86.

Boyden ES, Zhang F, Bamberg E, Nagel G, Deisseroth K (2005) Millisecond-timescale, genetically targeted optical control of neural activity. Nat Neurosci 8:1263–1268CrossRef

87.

Li X, Gutierrez DV, Hanson MG, Han J, Mark MD, Chiel H et al (2005) Fast noninvasive activation and inhibition of neural and network activity by vertebrate rhodopsin and green algae channelrhodopsin. Proc Natl Acad Sci U S A 102:17816–17821CrossRef

88.

Nagel G, Ollig D, Fuhrmann M, Kateriya S, Musti AM, Bamberg E et al (2002) Channelrhodopsin-1: a light-gated proton channel in green algae. Science 296:2395–2398CrossRef

89.

Zhao S, Cunha C, Zhang F, Liu Q, Gloss B, Deisseroth K et al (2008) Improved expression of halorhodopsin for light-induced silencing of neuronal activity. Brain Cell Biol 36:141–154CrossRef

90.

Gradinaru V, Thompson KR, Deisseroth K (2008) eNpHR: a Natronomonas halorhodopsin enhanced for optogenetic applications. Brain Cell Biol 36:129–139CrossRef

91.

Berndt A, Yizhar O, Gunaydin LA, Hegemann P, Deisseroth K (2009) Bi-stable neural state switches. Nat Neurosci 12:229–234CrossRef

92.

Yizhar O, Fenno LE, Prigge M, Schneider F, Davidson TJ, O'Shea DJ et al (2011) Neocortical excitation/inhibition balance in information processing and social dysfunction. Nature 477:171–178CrossRef

93.

Madisen L, Mao T, Koch H, Zhuo JM, Berenyi A, Fujisawa S et al (2012) A toolbox of Cre-dependent optogenetic transgenic mice for light-induced activation and silencing. Nat Neurosci 15:793–802CrossRef

94.

Madisen L, Garner AR, Shimaoka D, Chuong AS, Klapoetke NC, Li L et al (2015) Transgenic mice for intersectional targeting of neural sensors and effectors with high specificity and performance. Neuron 85:942–958CrossRef

95.

Tsien JZ, Chen DF, Gerber D, Tom C, Mercer EH, Anderson DJ et al (1996) Subregion- and cell type-restricted gene knockout in mouse brain. Cell 87:1317–1326CrossRef

96.

Bass CE, Grinevich VP, Vance ZB, Sullivan RP, Bonin KD, Budygin EA (2010) Optogenetic control of striatal dopamine release in rats. J Neurochem 114:1344–1352

97.

Witten IB, Lin SC, Brodsky M, Prakash R, Diester I, Anikeeva P et al (2010) Cholinergic interneurons control local circuit activity and cocaine conditioning. Science 330:1677–1681CrossRef

98.

Han X (2012) Optogenetics in the nonhuman primate. Prog Brain Res 196:215–233CrossRef

99.

Carter BJ (2005) Adeno-associated virus vectors in clinical trials. Hum Gene Ther 16:541–550CrossRef

100.

Lin JY, Knutsen PM, Muller A, Kleinfeld D, Tsien RY (2013) ReaChR: a red-shifted variant of channelrhodopsin enables deep transcranial optogenetic excitation. Nat Neurosci 16:1499–1508CrossRef

101.

Chuong AS, Miri ML, Busskamp V, Matthews GA, Acker LC, Sorensen AT et al (2014) Noninvasive optical inhibition with a red-shifted microbial rhodopsin. Nat Neurosci 17:1123–1129CrossRef

102.

Zhang J, Laiwalla F, Kim JA, Urabe H, Van Wagenen R, Song YK et al (2009) Integrated device for optical stimulation and spatiotemporal electrical recording of neural activity in light-sensitized brain tissue. J Neural Eng 6:055007CrossRef

103.

Zhang J, Laiwalla F, Kim JA, Urabe H, Van Wagenen R, Song YK et al (2009) A microelectrode array incorporating an optical waveguide device for stimulation and spatiotemporal electrical recording of neural activity. Conf Proc IEEE Eng Med Biol Soc 2009:2046–2049

104.

Chen S, Pei W, Gui Q, Chen Y, Zhao S, Wang H et al (2013) A fiber-based implantable multi-optrode array with contiguous optical and electrical sites. J Neural Eng 10:046020CrossRef

105.

Ozden I, Wang J, Lu Y, May T, Lee J, Goo W et al (2013) A coaxial optrode as multifunction write-read probe for optogenetic studies in non-human primates. J Neurosci Methods 219:142–154CrossRef

106.

Cao H, Gu L, Mohanty SK, Chiao JC (2013) An integrated muLED optrode for optogenetic stimulation and electrical recording. IEEE Trans Biomed Eng 60:225–229CrossRef

107.

Iwai Y, Honda S, Ozeki H, Hashimoto M, Hirase H (2011) A simple head-mountable LED device for chronic stimulation of optogenetic molecules in freely moving mice. Neurosci Res 70:124–127CrossRef

108.

Wentz CT, Bernstein JG, Monahan P, Guerra A, Rodriguez A, Boyden ES (2011) A wirelessly powered and controlled device for optical neural control of freely-behaving animals. J Neural Eng 8:046021CrossRef

109.

Warden MR, Cardin JA, Deisseroth K (2014) Optical neural interfaces. Annu Rev Biomed Eng 16:103–129CrossRef

110.

Davis GW (2006) Homeostatic control of neural activity: from phenomenology to molecular design. Annu Rev Neurosci 29:307–323CrossRef

111.

Davis GW, Goodman CS (1998) Genetic analysis of synaptic development and plasticity: homeostatic regulation of synaptic efficacy. Curr Opin Neurobiol 8:149–156CrossRef

112.

Marder E, Prinz AA (2002) Modeling stability in neuron and network function: the role of activity in homeostasis. Bioessays 24:1145–1154CrossRef

113.

Ginsberg MD, Sternau LL, Globus MY, Dietrich WD, Busto R (1992) Therapeutic modulation of brain temperature: relevance to ischemic brain injury. Cerebrovasc Brain Metab Rev 4:189–225

114.

Pérez-Otaño I, Ehlers MD (2005) Homeostatic plasticity and NMDA receptor trafficking. Trends Neurosci 28:229–238CrossRef

115.

Turrigiano GG, Nelson SB (2000) Hebb and homeostasis in neuronal plasticity. Curr Opin Neurobiol 10:358–364CrossRef

116.

Long MA, Fee MS (2008) Using temperature to analyse temporal dynamics in the songbird motor pathway. Nature 456:189–194CrossRef

117.

Andrasfalvy BK, Zemelman BV, Tang J, Vaziri A (2010) Two-photon single-cell optogenetic control of neuronal activity by sculpted light. Proc Natl Acad Sci U S A 107:11981–11986CrossRef

118.

Papagiakoumou E, Anselmi F, Bègue A, de Sars V, Glückstad J, Isacoff EY et al (2010) Scanless two-photon excitation of channelrhodopsin-2. Nat Methods 7:848–854CrossRef

119.

Roberts TF, Gobes SMH, Murugan M, Olveczky BP, Mooney R (2012) Motor circuits are required to encode a sensory model for imitative learning. Nat Neurosci 15:1454–1459

120.

Yizhar O, Fenno LE, Davidson TJ, Mogri M, Deisseroth K (2011) Optogenetics in neural systems. Neuron 71:9–34CrossRef

121.

Miyashita T, Shao YR, Chung J, Pourzia O, Feldman DE (2013) Long-term channelrhodopsin-2 (ChR2) expression can induce abnormal axonal morphology and targeting in cerebral cortex. Front Neural Circuits 7:8

Title: Implantable Optical Neural Interface
Authors: Sang Beom Jun
Yoonseob Lim
Publisher: Springer International Publishing
Book: Smart Sensors and Systems
Print ISBN: 978-3-319-33200-0

Electronic ISBN: 978-3-319-33201-7

Copyright Year: 2017
DOI: https://doi.org/10.1007/978-3-319-33201-7_9

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