Please use this identifier to cite or link to this item:
https://hdl.handle.net/10356/145372
Title: | Heterogeneous somatostatin-expressing neuron population in mouse ventral tegmental area | Authors: | Nagaeva, Elina Zubarev, Ivan Gonzales, Carolina Bengtsson Forss, Mikko Nikouei, Kasra de Miguel, Elena Elsilä, Lauri Linden, Anni-Maija Hjerling-Leffler, Jens Augustine, George James Korpi, Esa R. |
Keywords: | Science::Medicine | Issue Date: | 2020 | Source: | Nagaeva, E., Zubarev, I., Gonzales, C. B., Forss, M., Nikouei, K., de Miguel, E., . . . Korpi, E. R. (2020). Heterogeneous somatostatin-expressing neuron population in mouse ventral tegmental area. eLife, 9, 1-29. doi:10.7554/eLife.59328 | Project: | MOE2015-T2-2-095 MOE2017-T3-1-002 |
Journal: | eLife | Abstract: | The cellular architecture of the ventral tegmental area (VTA), the main hub of the brain reward system, remains only partially characterized. To extend the characterization to inhibitory neurons, we have identified three distinct subtypes of somatostatin (Sst)-expressing neurons in the mouse VTA. These neurons differ in their electrophysiological and morphological properties, anatomical localization, as well as mRNA expression profiles. Importantly, similar to cortical Sst-containing interneurons, most VTA Sst neurons express GABAergic inhibitory markers, but some of them also express glutamatergic excitatory markers and a subpopulation even express dopaminergic markers. Furthermore, only some of the proposed marker genes for cortical Sst neurons were expressed in the VTA Sst neurons. Physiologically, one of the VTA Sst neuron subtypes locally inhibited neighboring dopamine neurons. Overall, our results demonstrate the remarkable complexity and heterogeneity of VTA Sst neurons and suggest that these cells are multifunctional players in the midbrain reward circuitry. | URI: | https://hdl.handle.net/10356/145372 | ISSN: | 2050-084X | DOI: | 10.7554/eLife.59328 | Schools: | Lee Kong Chian School of Medicine (LKCMedicine) | Rights: | © 2020 Nagaeva et al. This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited. | Fulltext Permission: | open | Fulltext Availability: | With Fulltext |
Appears in Collections: | LKCMedicine Journal Articles |
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