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...

Celý popis

Uložené v:
Podrobná bibliografia
Vydané v:Neuron (Cambridge, Mass.) Ročník 88; číslo 6; s. 1136 - 1148
Hlavní autori: Wu, Fan, Stark, Eran, Ku, Pei-Cheng, Wise, Kensall D, Buzsáki, György, Yoon, Euisik
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: United States 16.12.2015
Predmet:
Animals
Behavior, Animal - physiology
Male
Mice
Mice, Inbred C57BL
Mice, Transgenic
Neurons - physiology
Optogenetics - instrumentation
Optogenetics - methods
Photic Stimulation - methods
Silicon
ISSN:1097-4199
On-line prístup:Zistit podrobnosti o prístupe
Tagy: Pridať tag
Žiadne tagy, Buďte prvý, kto otaguje tento záznam!
Popis
Shrnutí: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.
Bibliografia:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1097-4199
DOI:10.1016/j.neuron.2015.10.032