The transcriptomic and spatial organization of telencephalic GABAergic neuronal types.
Autor: | van Velthoven CTJ; Allen Institute for Brain Science, Seattle, WA, USA., Gao Y; Allen Institute for Brain Science, Seattle, WA, USA., Kunst M; Allen Institute for Brain Science, Seattle, WA, USA., Lee C; Allen Institute for Brain Science, Seattle, WA, USA., McMillen D; Allen Institute for Brain Science, Seattle, WA, USA., Chakka AB; Allen Institute for Brain Science, Seattle, WA, USA., Casper T; Allen Institute for Brain Science, Seattle, WA, USA., Clark M; Allen Institute for Brain Science, Seattle, WA, USA., Chakrabarty R; Allen Institute for Brain Science, Seattle, WA, USA., Daniel S; Allen Institute for Brain Science, Seattle, WA, USA., Dolbeare T; Allen Institute for Brain Science, Seattle, WA, USA., Ferrer R; Allen Institute for Brain Science, Seattle, WA, USA., Gloe J; Allen Institute for Brain Science, Seattle, WA, USA., Goldy J; Allen Institute for Brain Science, Seattle, WA, USA., Guzman J; Allen Institute for Brain Science, Seattle, WA, USA., Halterman C; Allen Institute for Brain Science, Seattle, WA, USA., Ho W; Allen Institute for Brain Science, Seattle, WA, USA., Huang M; Allen Institute for Brain Science, Seattle, WA, USA., James K; Allen Institute for Brain Science, Seattle, WA, USA., Nguy B; Allen Institute for Brain Science, Seattle, WA, USA., Pham T; Allen Institute for Brain Science, Seattle, WA, USA., Ronellenfitch K; Allen Institute for Brain Science, Seattle, WA, USA., Thomas ED; Allen Institute for Brain Science, Seattle, WA, USA., Torkelson A; Allen Institute for Brain Science, Seattle, WA, USA., Pagan CM; Allen Institute for Brain Science, Seattle, WA, USA., Kruse L; Allen Institute for Brain Science, Seattle, WA, USA., Dee N; Allen Institute for Brain Science, Seattle, WA, USA., Ng L; Allen Institute for Brain Science, Seattle, WA, USA., Waters J; Allen Institute for Brain Science, Seattle, WA, USA., Smith KA; Allen Institute for Brain Science, Seattle, WA, USA., Tasic B; Allen Institute for Brain Science, Seattle, WA, USA., Yao Z; Allen Institute for Brain Science, Seattle, WA, USA., Zeng H; Allen Institute for Brain Science, Seattle, WA, USA. |
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Jazyk: | angličtina |
Zdroj: | BioRxiv : the preprint server for biology [bioRxiv] 2024 Jun 18. Date of Electronic Publication: 2024 Jun 18. |
DOI: | 10.1101/2024.06.18.599583 |
Abstrakt: | The telencephalon of the mammalian brain comprises multiple regions and circuit pathways that play adaptive and integrative roles in a variety of brain functions. There is a wide array of GABAergic neurons in the telencephalon; they play a multitude of circuit functions, and dysfunction of these neurons has been implicated in diverse brain disorders. In this study, we conducted a systematic and in-depth analysis of the transcriptomic and spatial organization of GABAergic neuronal types in all regions of the mouse telencephalon and their developmental origins. This was accomplished by utilizing 611,423 single-cell transcriptomes from the comprehensive and high-resolution transcriptomic and spatial cell type atlas for the adult whole mouse brain we have generated, supplemented with an additional single-cell RNA-sequencing dataset containing 99,438 high-quality single-cell transcriptomes collected from the pre- and postnatal developing mouse brain. We present a hierarchically organized adult telencephalic GABAergic neuronal cell type taxonomy of 7 classes, 52 subclasses, 284 supertypes, and 1,051 clusters, as well as a corresponding developmental taxonomy of 450 clusters across different ages. Detailed charting efforts reveal extraordinary complexity where relationships among cell types reflect both spatial locations and developmental origins. Transcriptomically and developmentally related cell types can often be found in distant and diverse brain regions indicating that long-distance migration and dispersion is a common characteristic of nearly all classes of telencephalic GABAergic neurons. Additionally, we find various spatial dimensions of both discrete and continuous variations among related cell types that are correlated with gene expression gradients. Lastly, we find that cortical, striatal and some pallidal GABAergic neurons undergo extensive postnatal diversification, whereas septal and most pallidal GABAergic neuronal types emerge simultaneously during the embryonic stage with limited postnatal diversification. Overall, the telencephalic GABAergic cell type taxonomy can serve as a foundational reference for molecular, structural and functional studies of cell types and circuits by the entire community. Competing Interests: Competing Interests H.Z. is on the scientific advisory board of MapLight Therapeutics, Inc. The other authors declare no competing interests. |
Databáze: | MEDLINE |
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