• atlas of distinct cell populations

    From ScienceDaily@1:317/3 to All on Fri Apr 15 22:30:40 2022
    atlas of distinct cell populations
    The distinct cell populations were identified by single-nucleus RNA
    sequencing of 21,600 cells of the rat ventral tegmental area, located in the midbrain.

    Date:
    April 15, 2022
    Source:
    University of Alabama at Birmingham
    Summary:
    In a work of systematic biology that advances the field, researchers
    have identified 16 distinct cell populations in a complex area
    of the midbrain called the ventral tegmental area, or VTA. The
    VTA is important for its role in the dopamine neurotransmission
    involved in reward-directed behavior. Substance use disorders
    involve dysregulation of these reward circuits, leading to repeated
    drug-seeking despite adverse consequences.



    FULL STORY ==========================================================================
    In a work of systematic biology that advances the field, University
    of Alabama at Birmingham researchers have identified 16 distinct cell populations in a complex area of the midbrain called the ventral tegmental area, or VTA.


    ==========================================================================
    The VTA is important for its role in the dopamine neurotransmission
    involved in reward-directed behavior. Substance use disorders involve dysregulation of these reward circuits, leading to repeated drug-seeking despite adverse consequences. These include more than 100,000 drug
    overdose deaths in the United States in the most recent year. The VTA
    also has a role in several other neuropsychiatric disorders.

    Thus, expanding knowledge of its function is a start to explaining the mechanisms for substance use disorders involving drugs like cocaine,
    alcohol, opioids and nicotine, or psychiatric disorders like schizophrenia
    and attention deficit hyperactivity, or ADHD.

    Dopamine is one of the neurotransmitters used by the brain as chemical messengers to send signals between nerve cells. While decades of research
    have focused on dopaminergic neurotransmission in the VTA, there is also substantial evidence for the importance of two other neurotransmitters
    acting in the VTA in reward-related behaviors -- GABA and glutamate. There
    is also evidence for "combinatorial" neurons that can potentially
    synthesize and release multiple neurotransmitters. These suggest an
    additional layer of complexity in VTA cellular and synaptic function.

    Systematic biology is the science of classification, and it usually
    refers to the classification of organisms with regard to their natural relationships. The UAB VTA study classifies cell populations to extend and deepen previous work on the different cell types in the VTA, to provide
    a starting point for deciphering the relationships among these cells
    and their broad connections to other areas of the brain. The research, published in Cell Reports, was led by co-first authors Robert A. Phillips
    III and Jennifer J. Tuscher, Ph.D., and corresponding author Jeremy
    J. Day, Ph.D.

    The 16 distinct cell populations were identified by differences in gene expression after single-nucleus RNA sequencing of 21,600 cells from
    the rat VTA, creating a searchable online atlas of the VTA. The rat
    is the prime model for reward and substance use studies. This unbiased
    approach -- in contrast to previous studies that selected some subsets
    of cells for RNA sequencing -- was used to create the largest and most comprehensive single-cell transcriptomic analysis focused exclusively
    on the composition and molecular architecture of the VTA.



    ========================================================================== Though it was well known that the VTA is composed of heterogeneous cell
    types, the UAB atlas expands those studies in several key ways.

    "For example, previous single-cell sequencing studies were conducted exclusively in the mouse brain and have relied primarily on sequencing
    a subset of fluorescence-activated cell sorting-isolated midbrain
    dopaminergic populations, rather than sampling all VTA cell types,"
    Day said. "Notably, our sequencing dataset focuses exclusively on VTA sub-regions, unlike other studies that have focused on pooled cells from
    the mouse substantia nigra and VTA or a subset of fluorescently tagged
    cells from general midbrain regions." The 16 distinct cell populations
    include classic dopaminergic neurons, three subsets of glutamatergic
    neurons and three subsets of GABAergic neurons, as well as nine other
    cell types, including astrocytes and glial cells.

    After sub-clustering neuronal cells, the UAB researchers also identified
    four sub-clusters that may represent neurons capable of combinatorial neurotransmitter release. They also identified selective gene markers for classically defined dopamine neurons and for the combinatorial neurons. A selective marker allows viral targeting of distinct VTA subclasses for functional studies.

    The researchers also examined sub-clusters for opioid neuropeptides and
    their receptors, and identified pan-neuronal increased expression for risk genes associated with schizophrenia and "smoking initiation," as well as enrichment of ADHD risk genes in two glutamatergic neuronal populations.

    Co-authors besides Day, Phillips and Tuscher for the study, "An atlas of transcriptionally defined cell populations in the rat ventral tegmental
    area," are Samantha L. Black, Emma Andraka and N. Dalton Fitzgerald,
    UAB Department of Neurobiology and Evelyn F. McKnight Brain Institute;
    and Lara Ianov, Civitan International Research Center at UAB. Day,
    Phillips and Tuscher are, respectively, associate professor, graduate
    student and postdoctoral fellow in the UAB Department of Neurobiology.

    Support came from National Institutes of Health grants MH114990, DA039650
    and DA048348; UAB's Pittman Scholars Program, AMC21 Scholars Program and Civitan International Research Center; and a Brain and Behavior Research Foundation Young Investigator grant.


    ========================================================================== Story Source: Materials provided by
    University_of_Alabama_at_Birmingham. Original written by Jeff
    Hansen. Note: Content may be edited for style and length.


    ========================================================================== Journal Reference:
    1. Robert A. Phillips, Jennifer J. Tuscher, Samantha L. Black,
    Emma Andraka,
    N. Dalton Fitzgerald, Lara Ianov, Jeremy J. Day. An atlas of
    transcriptionally defined cell populations in the rat ventral
    tegmental area. Cell Reports, 2022; 39 (1): 110616 DOI: 10.1016/
    j.celrep.2022.110616 ==========================================================================

    Link to news story: https://www.sciencedaily.com/releases/2022/04/220415163751.htm

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