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

  • Jack F. Webster
  • , Rozan Vroman
  • , Sanne Beerens
  • , Shuzo Sakata
  • , Christian Wozny

Research output: Contribution to Journal › Article › Academic › peer-review

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 subpopulation. 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.
Original languageEnglish
Pages (from-to)3561-3575
Number of pages15
JournalEuropean Journal of Neuroscience
Volume53
Issue number11
Early online date18 Apr 2021
DOIs
Publication statusPublished - Jun 2021
Externally publishedYes

Funding

We thank Peer Wulff for insightful discussions and critical comments on an earlier version of the manuscript. We are also grateful to Hongkui Zeng from the Allen Brain Institute, Seattle, for kindly sharing the Ai9 reporter mice with us, and we thank Csaba F?ldy, Brain Research Institute, University of Zurich, Switzerland, for generously providing us with NPY-hrGFP mice. In addition, we would like to acknowledge the help of Yoshiko Hashikawa, Koichi Hashikawa, and Garret Stuber for sharing their data and the cluster analysis of lateral habenula neurons. The work was supported by the Royal Society (Research Grant RG160549, CW), Tenovus Scotland (Project S16/19, CW), the Wellcome Trust (205917/z/17/Z, CW), and the BBSRC (BB/M00905X/1, SS). JFW held a studentship funded by the Engineering and Physical Sciences Research Council (EPSRC). We thank Peer Wulff for insightful discussions and critical comments on an earlier version of the manuscript. We are also grateful to Hongkui Zeng from the Allen Brain Institute, Seattle, for kindly sharing the Ai9 reporter mice with us, and we thank Csaba Földy, Brain Research Institute, University of Zurich, Switzerland, for generously providing us with NPY‐hrGFP mice. In addition, we would like to acknowledge the help of Yoshiko Hashikawa, Koichi Hashikawa, and Garret Stuber for sharing their data and the cluster analysis of lateral habenula neurons. The work was supported by the Royal Society (Research Grant RG160549, CW), Tenovus Scotland (Project S16/19, CW), the Wellcome Trust (205917/z/17/Z, CW), and the BBSRC (BB/M00905X/1, SS). JFW held a studentship funded by the Engineering and Physical Sciences Research Council (EPSRC).

FundersFunder number
Allen Brain Institute
Universität Zürich
Brain Research Institute
Engineering and Physical Sciences Research Council
UK Research and Innovation
Biotechnology and Biological Sciences Research CouncilBB/M00905X/1
TenovusS16/19
Wellcome Trust205917/z/17/Z
Royal SocietyRG160549

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