Abstract

Juxtaglomerular cells (JGCs) of the olfactory bulb (OB) glomerular layer (GL) play a fundamental role in olfactory information processing. Their variability in morphology, physiology, and connectivity suggests distinct functions. The quantitative understanding of population-wise morphological and physiological properties and a comprehensive classification based on quantitative parameters, however, is still lacking, impeding the analysis of microcircuits. Here, we provide multivariate clustering of 95 in vitro sampled cells from the GL of the mouse (male or female C57BL/6) OB and perform detailed morphological and physiological characterization for the seven computed JGC types. Using a classifier based on a subselection of parameters, we identified the neuron types in paired recordings to characterize their functional connectivity. We found that 4 of the 7 clusters comply with prevailing concepts of GL cell types, whereas the other 3 represent own distinct entities. We have labeled these entities horizontal superficial tufted cell (hSTC), vertical superficial tufted cell, and microglomerular cell (MGC): The hSTC is a tufted cell with a lateral dendrite that much like mitral cells and tufted cells receives excitatory inputs from the external tufted cell but likewise serves as an excitatory element for glomerular interneurons. The vertical superficial tufted cell, on the other hand, represents a tufted cell type with vertically projecting basal dendrites. We further define the MGC, characterized by a small dendritic tree and plateau action potentials. In addition to olfactory nerve-driven and external tufted cell driven interneurons, these MGCs represent a third functionally distinct type, the hSTC-driven interneurons. The presented correlative analysis helps to bridge the gap between branching patterns and cellular functional properties, permitting the integration of results from in vivo recordings, advanced morphological tools, and connectomics.SIGNIFICANCE STATEMENT The variance of neuron properties is a feature across mammalian cerebral circuits, contributing to signal processing and adding computational robustness to the networks. It is particularly noticeable in the glomerular layer of the olfactory bulb, the first site of olfactory information processing. We provide the first unbiased population-wise multivariate analysis to correlate morphological and physiological parameters of juxtaglomerular cells. We identify seven cell types, including four previously described neuron types, and identify further three distinct classes. The presented correlative analysis of morphological and physiological parameters gives an opportunity to predict morphological classes from physiological measurements or the functional properties of neurons from morphology and opens the way to integrate results from in vivo recordings, advanced morphological tools, and connectomics.

Highlights

  • A fundamental property of mammalian cerebral networks is their broad functional and morphological tuning (Parra et al., 1998; Markram et al, 2004; Marder, 2011; Kepecs and Fishell, 2014)

  • Because our goal was an objective population-wise classification of glomerular layer (GL) cell types, we acquired a broad sample of Juxtaglomerular cells (JGCs) containing both Projection neurons (PNs) and INs

  • Four types of juxtaglomerular INs within the olfactory bulb (OB) GL Broad functional and morphological variability of neurons is a key characteristic of vertebrate brain networks (Parra et al, 1998; Markram et al, 2004; Marder, 2011; Kepecs and Fishell, 2014), present in the GL, the most superficial layer of the OB

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Summary

Introduction

A fundamental property of mammalian cerebral networks is their broad functional and morphological tuning (Parra et al., 1998; Markram et al, 2004; Marder, 2011; Kepecs and Fishell, 2014). Projection neurons (PNs) and interneurons (INs) exhibit striking morphologic variance, rendering the definition of pri-. Received Jan. 29, 2018; revised June 4, 2018; accepted June 22, 2018. (FC001153), the U.K. Medical Research Council (FC001153), and the Wellcome Trust (FC001153); the Max-Planck-Society; and U.K. Medical Research Council Grant MC_UP_1202/5.

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