Monolithically Integrated μLEDs on Silicon Neural Probes for High-Resolution Optogenetic Studies in Behaving Animals

We report a scalable method to monolithically integrate microscopic light emitting diodes (μLEDs) and recording sites onto silicon neural probes for optogenetic applications in neuroscience. Each μLED and recording site has dimensions similar to a pyramidal neuron soma, providing confined emission a...

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Vydáno v:Neuron (Cambridge, Mass.) Ročník 88; číslo 6; s. 1136 - 1148
Hlavní autoři: Wu, Fan, Stark, Eran, Ku, Pei-Cheng, Wise, Kensall D, Buzsáki, György, Yoon, Euisik
Médium: Journal Article
Jazyk:angličtina
Vydáno: United States 16.12.2015
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ISSN:1097-4199
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Abstract We report a scalable method to monolithically integrate microscopic light emitting diodes (μLEDs) and recording sites onto silicon neural probes for optogenetic applications in neuroscience. Each μLED and recording site has dimensions similar to a pyramidal neuron soma, providing confined emission and electrophysiological recording of action potentials and local field activity. We fabricated and implanted the four-shank probes, each integrated with 12 μLEDs and 32 recording sites, into the CA1 pyramidal layer of anesthetized and freely moving mice. Spikes were robustly induced by 60 nW light power, and fast population oscillations were induced at the microwatt range. To demonstrate the spatiotemporal precision of parallel stimulation and recording, we achieved independent control of distinct cells ∼ 50 μm apart and of differential somato-dendritic compartments of single neurons. The scalability and spatiotemporal resolution of this monolithic optogenetic tool provides versatility and precision for cellular-level circuit analysis in deep structures of intact, freely moving animals.
AbstractList We report a scalable method to monolithically integrate microscopic light emitting diodes (μLEDs) and recording sites onto silicon neural probes for optogenetic applications in neuroscience. Each μLED and recording site has dimensions similar to a pyramidal neuron soma, providing confined emission and electrophysiological recording of action potentials and local field activity. We fabricated and implanted the four-shank probes, each integrated with 12 μLEDs and 32 recording sites, into the CA1 pyramidal layer of anesthetized and freely moving mice. Spikes were robustly induced by 60 nW light power, and fast population oscillations were induced at the microwatt range. To demonstrate the spatiotemporal precision of parallel stimulation and recording, we achieved independent control of distinct cells ∼ 50 μm apart and of differential somato-dendritic compartments of single neurons. The scalability and spatiotemporal resolution of this monolithic optogenetic tool provides versatility and precision for cellular-level circuit analysis in deep structures of intact, freely moving animals.
Author Buzsáki, György
Wu, Fan
Ku, Pei-Cheng
Wise, Kensall D
Stark, Eran
Yoon, Euisik
Author_xml – sequence: 1
  givenname: Fan
  surname: Wu
  fullname: Wu, Fan
  organization: Department of Electrical Engineering and Computer Science, University of Michigan, 1301 Beal Avenue, Ann Arbor, MI 48109-2122, USA
– sequence: 2
  givenname: Eran
  surname: Stark
  fullname: Stark, Eran
  organization: NYU Neuroscience Institute, East River Science Park, Alexandria Center, 450 East 29th Street, 9th Floor, New York, NY 10016, USA; Department of Physiology and Pharmacology, Sackler Faculty of Medicine, Tel Aviv University, 69978 Tel Aviv, Israel; Sagol School of Neuroscience, Tel Aviv University, 69978 Tel Aviv, Israel
– sequence: 3
  givenname: Pei-Cheng
  surname: Ku
  fullname: Ku, Pei-Cheng
  organization: Department of Electrical Engineering and Computer Science, University of Michigan, 1301 Beal Avenue, Ann Arbor, MI 48109-2122, USA
– sequence: 4
  givenname: Kensall D
  surname: Wise
  fullname: Wise, Kensall D
  organization: Department of Electrical Engineering and Computer Science, University of Michigan, 1301 Beal Avenue, Ann Arbor, MI 48109-2122, USA
– sequence: 5
  givenname: György
  surname: Buzsáki
  fullname: Buzsáki, György
  email: gyorgy.buzsaki@nyumc.org
  organization: NYU Neuroscience Institute, East River Science Park, Alexandria Center, 450 East 29th Street, 9th Floor, New York, NY 10016, USA. Electronic address: gyorgy.buzsaki@nyumc.org
– sequence: 6
  givenname: Euisik
  surname: Yoon
  fullname: Yoon, Euisik
  email: esyoon@umich.edu
  organization: Department of Electrical Engineering and Computer Science, University of Michigan, 1301 Beal Avenue, Ann Arbor, MI 48109-2122, USA. Electronic address: esyoon@umich.edu
BackLink https://www.ncbi.nlm.nih.gov/pubmed/26627311$$D View this record in MEDLINE/PubMed
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– reference: 19167428 - J Neurosci Methods. 2009 Apr 30;179(1):90-100
– reference: 9492204 - J Comp Neurol. 1998 Feb 16;391(3):335-52
– reference: 25856489 - Neuron. 2015 Apr 8;86(1):92-105
– reference: 25033186 - Neuron. 2014 Jul 16;83(2):467-80
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Snippet We report a scalable method to monolithically integrate microscopic light emitting diodes (μLEDs) and recording sites onto silicon neural probes for...
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SubjectTerms Animals
Behavior, Animal - physiology
Male
Mice
Mice, Inbred C57BL
Mice, Transgenic
Neurons - physiology
Optogenetics - instrumentation
Optogenetics - methods
Photic Stimulation - methods
Silicon
Title Monolithically Integrated μLEDs on Silicon Neural Probes for High-Resolution Optogenetic Studies in Behaving Animals
URI https://www.ncbi.nlm.nih.gov/pubmed/26627311
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