NDNF is selectively expressed by neocortical, but not habenular neurogliaform cells

Webster, Jack F. and Vroman, Rozan and Beerens, Sanne and Sakata, Shuzo and Wozny, Christian (2021) NDNF is selectively expressed by neocortical, but not habenular neurogliaform cells. European Journal of Neuroscience, 53 (11). pp. 3561-3575. ISSN 0953-816X (https://doi.org/10.1111/ejn.15237)

[thumbnail of Webster-etal-EJN-2021-NDNF-is-selectively-expressed-by-neocortical-but-not-habenular-neurogliaform-cells]
Preview
Text. Filename: Webster_etal_EJN_2021_NDNF_is_selectively_expressed_by_neocortical_but_not_habenular_neurogliaform_cells.pdf
Final Published Version
License: Creative Commons Attribution 4.0 logo

Download (3MB)| Preview

Abstract

The lateral habenula (LHb) is a brain structure which is known to be pathologically hyperactive in depression, whereby it shuts down the brains' reward systems. Interestingly, inhibition of the LHb has been shown to have an antidepressant effect, hence making the LHb a fascinating subject of study for developing novel antidepressant therapies. Despite this however, the exact mechanisms by which inhibitory signalling is processed within the LHb remain incompletely understood. Some studies have proposed the existence of locally‐targeting inhibitory interneuron populations within the LHb. One such population is believed to be akin to neocortical neurogliaform cells, yet specific molecular markers for studying these neurons are sparse and hence their function remains elusive. Recently, neuron‐derived neurotrophic factor (NDNF) has been proposed as one such marker for neocortical neurogliaform cells. Using a combination of histological, physiological and optogenetic tools, we hence sought to first validate if NDNF was selectively expressed by such inhibitory neurons within the neocortex, and then if it was confined to a similar population within the LHb. While we report this to be true for the neocortex, we find no such evidence within the LHb; rather that NDNF is expressed without restriction to a particular neuronal sub‐population. These results hence indicate that molecular markers can represent broadly diverse populations of neurons on a region‐to‐region basis, and that therefore each population as defined by molecular marker expression should be validated in each brain structure.