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Stimulus dependent diversity and stereotypy in the output of an olfactory functional unit

Author

Listed:
  • Ezequiel M. Arneodo

    (NYU Langone Health
    University of California San Diego)

  • Kristina B. Penikis

    (NYU Langone Health
    New York University)

  • Neil Rabinowitz

    (New York University
    Howard Hughes Medical Institute
    DeepMind, 6 Pancras Square)

  • Angela Licata

    (NYU Langone Health)

  • Annika Cichy

    (Northwestern University)

  • Jingji Zhang

    (Northwestern University)

  • Thomas Bozza

    (Northwestern University)

  • Dmitry Rinberg

    (NYU Langone Health
    New York University)

Abstract

Olfactory inputs are organized in an array of functional units (glomeruli), each relaying information from sensory neurons expressing a given odorant receptor to a small population of output neurons, mitral/tufted (MT) cells. MT cells respond heterogeneously to odorants, and how the responses encode stimulus features is unknown. We recorded in awake mice responses from “sister” MT cells that receive input from a functionally characterized, genetically identified glomerulus, corresponding to a specific receptor (M72). Despite receiving similar inputs, sister MT cells exhibit temporally diverse, concentration-dependent, excitatory and inhibitory responses to most M72 ligands. In contrast, the strongest known ligand for M72 elicits temporally stereotyped, early excitatory responses in sister MT cells, consistent across a range of concentrations. Our data suggest that information about ligand affinity is encoded in the collective stereotypy or diversity of activity among sister MT cells within a glomerular functional unit in a concentration-tolerant manner.

Suggested Citation

  • Ezequiel M. Arneodo & Kristina B. Penikis & Neil Rabinowitz & Angela Licata & Annika Cichy & Jingji Zhang & Thomas Bozza & Dmitry Rinberg, 2018. "Stimulus dependent diversity and stereotypy in the output of an olfactory functional unit," Nature Communications, Nature, vol. 9(1), pages 1-13, December.
  • Handle: RePEc:nat:natcom:v:9:y:2018:i:1:d:10.1038_s41467-018-03837-1
    DOI: 10.1038/s41467-018-03837-1
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    Cited by:

    1. Carles Bosch & Tobias Ackels & Alexandra Pacureanu & Yuxin Zhang & Christopher J. Peddie & Manuel Berning & Norman Rzepka & Marie-Christine Zdora & Isabell Whiteley & Malte Storm & Anne Bonnin & Chris, 2022. "Functional and multiscale 3D structural investigation of brain tissue through correlative in vivo physiology, synchrotron microtomography and volume electron microscopy," Nature Communications, Nature, vol. 13(1), pages 1-16, December.
    2. Jane S. Huang & Tenzin Kunkhyen & Alexander N. Rangel & Taryn R. Brechbill & Jordan D. Gregory & Emily D. Winson-Bushby & Beichen Liu & Jonathan T. Avon & Ryan J. Muggleton & Claire E. J. Cheetham, 2022. "Immature olfactory sensory neurons provide behaviourally relevant sensory input to the olfactory bulb," Nature Communications, Nature, vol. 13(1), pages 1-19, December.

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