An optrode array for spatiotemporally-precise large-scale optogenetic stimulation of deep cortical layers in non-human primates

Andrew M. Clark, Alexander Ingold, Christopher F. Reiche, Donald Cundy III, Justin L. Balsor, Frederick Federer, Niall McAlinden, Yunzhou Cheng, John D. Rolston, Loren Rieth, Martin D. Dawson, Keith Mathieson, Steve Blair, Alessandra Angelucci

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6 Citations (Scopus)
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Abstract

Optogenetics has transformed studies of neural circuit function, but remains challenging to apply to non-human primates (NHPs). A major challenge is delivering intense, spatiotemporally-precise, patterned photostimulation across large volumes in deep tissue. Such stimulation is critical, for example, to modulate selectively deep-layer corticocortical feedback circuits. To address this need, we have developed the Utah Optrode Array (UOA), a 10×10 glass needle waveguide array fabricated atop a novel opaque optical interposer, and bonded to an electrically addressable µLED array. In vivo experiments with the UOA demonstrated large-scale, spatiotemporally precise, activation of deep circuits in NHP cortex. Specifically, the UOA permitted both focal (confined to single layers/columns), and widespread (multiple layers/columns) optogenetic activation of deep layer neurons, as assessed with multi-channel laminar electrode arrays, simply by varying the number of activated µLEDs and/or the irradiance. Thus, the UOA represents a powerful optoelectronic device for targeted manipulation of deep-layer circuits in NHP models.
Original languageEnglish
Article number329
Number of pages18
JournalCommunications Biology
Volume7
DOIs
Publication statusPublished - 14 Mar 2024

Funding

We thank Kesi Sainsbury for histological assistance, Seminare Ta’afua for help with experiments, and Julian Haberland and Christine Kallmayer at the Fraunhofer-Institut für Zuverlässigkeit und Mikrointegration (IZM) for µLED-to-interposer bonding. This work was supported primarily by a BRAIN grant (U01 NS099702) from the National Institute of Health (NIH) to S.B., A.A. L.R., and K.M. Additional support was provided by grants from the NIH (R01 EY026812, R01 EY019743, and R01 EY031959), the National Science Foundation (IOS 1755431), and the Mary Boesche endowed Chair, to A.A., and an unrestricted grant from Research to Prevent Blindness, Inc. and a core grant from the NIH (P30 EY014800) to the Department of Ophthalmology, University of Utah. K.M. acknowledges support from the Royal Academy of Engineering through their Chair in Emerging Technologies scheme.

Keywords

  • extracellular recording
  • striate cortex

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