Strathclyde Institute for Pharmacy and Biomedical Sciences, University of Strathclyde, Glasgow, UK.
MSH Medical School Hamburg, Medical University, Hamburg, Germany.
Eur J Neurosci. 2021 Jun;53(11):3561-3575. doi: 10.1111/ejn.15237. Epub 2021 May 7.
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.
外侧缰核(LHb)是一种已知在抑郁症中病理性过度活跃的脑结构,它会关闭大脑的奖励系统。有趣的是,抑制 LHb 已被证明具有抗抑郁作用,因此 LHb 成为开发新型抗抑郁疗法的迷人研究课题。然而,尽管如此,抑制信号在 LHb 内的处理的确切机制仍不完全清楚。一些研究提出了 LHb 内存在局部靶向抑制性中间神经元群体的存在。其中一种群体类似于新皮层神经胶质细胞,但用于研究这些神经元的特定分子标记物稀缺,因此其功能仍然难以捉摸。最近,神经元衍生的神经营养因子(NDNF)被提议作为新皮层神经胶质细胞的一种标记物。我们使用组织学、生理学和光遗传学工具的组合,首先试图验证 NDNF 是否被新皮层中的此类抑制性神经元选择性表达,然后验证它是否局限于 LHb 中的类似群体。虽然我们报告了这在新皮层中是正确的,但我们在 LHb 中没有发现这样的证据;相反,NDNF 的表达不受特定神经元亚群的限制。这些结果表明,分子标记物可以根据区域到区域的基础代表广泛多样化的神经元群体,因此,应在每个脑结构中验证通过分子标记物表达定义的每个群体。