Abstract

Hippocampal interneurons comprise a diverse family of inhibitory neurons that are critical for detailed information processing. Along with gamma-aminobutyric acid (GABA), interneurons secrete a myriad of neuroactive substances via secretory vesicles but the molecular composition and regulatory mechanisms remain largely unknown. In this study, we have carried out an immunohistofluorescence analysis to describe the molecular content of vesicles in distinct populations of hippocampal neurons. Our results indicate that phogrin, an integral protein of secretory vesicles in neuroendocrine cells, is highly enriched in parvalbumin-positive interneurons. Consistently, immunoelectron microscopy revealed phogrin staining in axon terminals of symmetrical synapses establishing inhibitory contacts with cell bodies of CA1 pyramidal neurons. Furthermore, phogrin is highly expressed in CA3 and dentate gyrus (DG) interneurons which are both positive for PV and neuropeptide Y. Surprisingly, chromogranin B a canonical large dense core vesicle marker, is excluded from inhibitory cells in the hippocampus but highly expressed in excitatory CA3 pyramidal neurons and DG granule cells. Our results provide the first evidence of phogrin expression in hippocampal interneurons and suggest the existence of molecularly distinct populations of secretory vesicles in different types of inhibitory neurons.

Highlights

  • GABAergic neurons in the mammalian central nervous system (CNS) comprise a number of interneuronal subgroups that assemble into networks with specific synaptic properties and functional roles

  • To identify the molecular composition of secretory vesicles in different hippocampal interneuron subtypes, we started by characterizing the expression pattern of canonical Large Dense Core Vesicles (LDCVs) markers calcium-activator proteins for secretion (CAPS)-1 and chromogranin B (Speidel et al, 2003; Machado et al, 2010)

  • Our results indicate that both LDCV-associated proteins CAPS1 and chromogranin B are not highly expressed in hippocampal interneurons

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Summary

Introduction

GABAergic neurons in the mammalian central nervous system (CNS) comprise a number of interneuronal subgroups that assemble into networks with specific synaptic properties and functional roles (reviewed in Freund and Buzsáki, 1996; McBain and Fisahn, 2001; Klausberger and Somogyi, 2008). Recent advances in understanding neuropeptide signaling suggest that the interneuronal system of neuropeptides is crucial for maintaining appropriate brain function. It is currently unknown how interneurons regulate neuropeptide storage and release to modulate synaptic transmission and information processing. This lack in our knowledge is in stark contrast to the detailed mechanistic insights. A better understanding of the role of neuropeptide secretion in different interneuron types is necessary to unveil their function in regulating neuronal networks

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