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Ex Vivo Functional Characterization of Mouse Olfactory Bulb Projection Neurons Reveals a Heterogeneous Continuum.

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Peer-reviewed

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Abstract

Mitral cells (MCs) and tufted cells (TCs) in the olfactory bulb (OB) act as an input convergence hub and transmit information to higher olfactory areas. Since first characterized, they have been classed as distinct projection neurons based on size and location: laminarly arranged MCs with a diameter larger than 20 µm in the mitral layer (ML) and smaller TCs spread across both the ML and external plexiform layers (EPL). Recent in vivo work has shown that these neurons encode complementary olfactory information, akin to parallel channels in other sensory systems. Yet, many ex vivo studies still collapse them into a single class, mitral/tufted, when describing their physiological properties and impact on circuit function. Using immunohistochemistry and whole-cell patch-clamp electrophysiology in fixed or acute slices from adult mice, we attempted to align in vivo and ex vivo data and test a soma size-based classifier of bulbar projection neurons using passive and intrinsic firing properties. We found that there is no clear separation between cell types based on passive or active properties. Rather, there is a heterogeneous continuum with three loosely clustered subgroups: TCs in the EPL, and putative tufted or putative MCs in the ML. These findings illustrate the large functional heterogeneity present within the OB projection neurons and complement existing literature highlighting how heterogeneity in sensory systems is preponderant and possibly used in the OB to decode complex olfactory information.

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Journal Title

eNeuro

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Journal ISSN

2373-2822
2373-2822

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Publisher

Society for Neuroscience

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Except where otherwised noted, this item's license is described as Attribution 4.0 International
Sponsorship
Royal Society (RGS/R1/191481)
BBSRC (BB/W014688/1)
MRC (MC_PC_MR/X012271/1)
This work was supported by a UKRI Medical Research Council Equipment Grant (MC_PC_MR/X012271/1) and project grants from the Royal Society (RGS\R1\19148), the URKI Biotechnology and Biological Sciences Research Council (BB\W014688\1) and the Newton Trust (EG); an Icelandic Research Fund Project Grant 217945-051 (PHP,EG); a Cambridge Trust PhD studentship (LH); and a University of Cambridge Institute of Neuroscience postgraduate scholarship (SJBW).

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