An overview of human single-cell RNA sequencing studies in neurobiological disease
Neurobiological disorders are highly prevalent medical conditions that contribute to significant morbidity and mortality. Single-cell RNA sequencing (scRNA-seq) is a technique that measures gene expression in individual cells. In this review, we survey scRNA-seq studies of tissues from patients suff...
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Veröffentlicht in: | Neurobiology of disease 2023-08, Vol.184, p.106201-106201, Article 106201 |
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Sprache: | eng |
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Zusammenfassung: | Neurobiological disorders are highly prevalent medical conditions that contribute to significant morbidity and mortality. Single-cell RNA sequencing (scRNA-seq) is a technique that measures gene expression in individual cells. In this review, we survey scRNA-seq studies of tissues from patients suffering from neurobiological disease. This includes postmortem human brains and organoids derived from peripheral cells. We highlight a range of conditions, including epilepsy, cognitive disorders, substance use disorders, and mood disorders. These findings provide new insights into neurobiological disease in multiple ways, including discovering novel cell types or subtypes involved in disease, proposing new pathophysiological mechanisms, uncovering novel drug targets, or identifying potential biomarkers. We discuss the quality of these findings and suggest potential future directions and areas open for additional research, including studies of non-cortical brain regions and additional conditions such as anxiety disorders, mood disorders, and sleeping disorders. We argue that additional scRNA-seq of tissues from patients suffering from neurobiological disease could advance our understanding and treatment of these conditions.
•scRNA-seq of human tissue can improve understanding of neurobiological disease.•scRNA-seq studies identified novel molecular and cellular aspects of neurobiological disease.•Additional scRNA-seq of human neurobiological disease is needed to improve therapy. |
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ISSN: | 0969-9961 1095-953X 1095-953X |
DOI: | 10.1016/j.nbd.2023.106201 |