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Multichannel optogenetics combined with laminar recordings for ultra-controlled neuronal interrogation

Author

Listed:
  • David Eriksson

    (University of Freiburg
    University of Freiburg)

  • Artur Schneider

    (University of Freiburg)

  • Anupriya Thirumalai

    (University of Freiburg
    University Medical Center Göttingen)

  • Mansour Alyahyay

    (University of Freiburg)

  • Brice Crompe

    (University of Freiburg)

  • Kirti Sharma

    (University of Freiburg)

  • Patrick Ruther

    (University of Freiburg)

  • Ilka Diester

    (University of Freiburg
    Bernstein Center Freiburg. Hansastr. 9a)

Abstract

Simultaneous large-scale recordings and optogenetic interventions may hold the key to deciphering the fast-paced and multifaceted dialogue between neurons that sustains brain function. Here we have taken advantage of thin, cell-sized, optical fibers for minimally invasive optogenetics and flexible implantations. We describe a simple procedure for making those fibers side-emitting with a Lambertian emission distribution. Here we combined those fibers with silicon probes to achieve high-quality recordings and ultrafast multichannel optogenetic inhibition. Furthermore, we developed a multi-channel optical commutator and general-purpose patch-cord for flexible experiments. We demonstrate that our framework allows to conduct simultaneous laminar recordings and multifiber stimulations, 3D optogenetic stimulation, connectivity inference, and behavioral quantification in freely moving animals. Our framework paves the way for large-scale photo tagging and controlled interrogation of rapid neuronal communication in any combination of brain areas.

Suggested Citation

  • David Eriksson & Artur Schneider & Anupriya Thirumalai & Mansour Alyahyay & Brice Crompe & Kirti Sharma & Patrick Ruther & Ilka Diester, 2022. "Multichannel optogenetics combined with laminar recordings for ultra-controlled neuronal interrogation," Nature Communications, Nature, vol. 13(1), pages 1-13, December.
  • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-28629-6
    DOI: 10.1038/s41467-022-28629-6
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    References listed on IDEAS

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    1. Tingying Peng & Kurt Thorn & Timm Schroeder & Lichao Wang & Fabian J. Theis & Carsten Marr & Nassir Navab, 2017. "A BaSiC tool for background and shading correction of optical microscopy images," Nature Communications, Nature, vol. 8(1), pages 1-7, August.
    2. Mathias Mahn & Lihi Gibor & Pritish Patil & Katayun Cohen-Kashi Malina & Shir Oring & Yoav Printz & Rivka Levy & Ilan Lampl & Ofer Yizhar, 2018. "High-efficiency optogenetic silencing with soma-targeted anion-conducting channelrhodopsins," Nature Communications, Nature, vol. 9(1), pages 1-15, December.
    3. Johannes Vierock & Silvia Rodriguez-Rozada & Alexander Dieter & Florian Pieper & Ruth Sims & Federico Tenedini & Amelie C. F. Bergs & Imane Bendifallah & Fangmin Zhou & Nadja Zeitzschel & Joachim Ahlb, 2021. "BiPOLES is an optogenetic tool developed for bidirectional dual-color control of neurons," Nature Communications, Nature, vol. 12(1), pages 1-20, December.
    4. James J. Jun & Nicholas A. Steinmetz & Joshua H. Siegle & Daniel J. Denman & Marius Bauza & Brian Barbarits & Albert K. Lee & Costas A. Anastassiou & Alexandru Andrei & Çağatay Aydın & Mladen Barbic &, 2017. "Fully integrated silicon probes for high-density recording of neural activity," Nature, Nature, vol. 551(7679), pages 232-236, November.
    5. Julien Courtin & Fabrice Chaudun & Robert R. Rozeske & Nikolaos Karalis & Cecilia Gonzalez-Campo & Hélène Wurtz & Azzedine Abdi & Jerome Baufreton & Thomas C. M. Bienvenu & Cyril Herry, 2014. "Prefrontal parvalbumin interneurons shape neuronal activity to drive fear expression," Nature, Nature, vol. 505(7481), pages 92-96, January.
    6. Britton A. Sauerbrei & Jian-Zhong Guo & Jeremy D. Cohen & Matteo Mischiati & Wendy Guo & Mayank Kabra & Nakul Verma & Brett Mensh & Kristin Branson & Adam W. Hantman, 2020. "Cortical pattern generation during dexterous movement is input-driven," Nature, Nature, vol. 577(7790), pages 386-391, January.
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