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从恒河猴和人类杏仁核亚核细胞类型变化中获得的转化见解。

Translational Insights From Cell Type Variation Across Amygdala Subnuclei in Rhesus Monkeys and Humans.

机构信息

Department of Psychology (Kamboj, Fox), California National Primate Research Center (Kamboj, Bauman, Fox), and MIND Institute (Carlson, Ander, Hanson, Bauman, Schumann), University of California, Davis; Department of Psychiatry and Behavioral Sciences (Carlson, Hanson, Schumann), Department of Neurology (Ander), and Department of Physiology and Membrane Biology (Murray, Bauman), School of Medicine, University of California, Davis; Department of Neuroscience and Department of Psychiatry, School of Medicine and Dentistry, University of Rochester, Rochester, NY (Fudge).

出版信息

Am J Psychiatry. 2024 Dec 1;181(12):1086-1102. doi: 10.1176/appi.ajp.20230602. Epub 2024 Oct 30.

Abstract

OBJECTIVE

Theories of amygdala function are central to our understanding of psychiatric and neurodevelopmental disorders. However, limited knowledge of the molecular and cellular composition of the amygdala impedes translational research aimed at developing new treatments and interventions. The aim of this study was to characterize and compare the composition of amygdala cells to help bridge the gap between preclinical models and human psychiatric and neurodevelopmental disorders.

METHODS

Tissue was dissected from multiple amygdala subnuclei in both humans (N=3, male) and rhesus macaques (N=3, male). Single-nucleus RNA sequencing was performed to characterize the transcriptomes of individual nuclei.

RESULTS

The results reveal substantial heterogeneity between regions, even when restricted to inhibitory or excitatory neurons. Consistent with previous work, the data highlight the complexities of individual marker genes for uniquely targeting specific cell types. Cross-species analyses suggest that the rhesus monkey model is well-suited to understanding the human amygdala, but also identify limitations. For example, a cell cluster in the ventral lateral nucleus of the amygdala (vLa) is enriched in humans relative to rhesus macaques. Additionally, the data describe specific cell clusters with relative enrichment of disorder-related genes. These analyses point to the human-enriched vLa cell cluster as relevant to autism spectrum disorder, potentially highlighting a vulnerability to neurodevelopmental disorders that has emerged in recent primate evolution. Further, a cluster of cells expressing markers for intercalated cells is enriched for genes reported in human genome-wide association studies of neuroticism, anxiety disorders, and depressive disorders.

CONCLUSIONS

Together, these findings shed light on the composition of the amygdala and identify specific cell types that can be prioritized in basic science research to better understand human psychopathology and guide the development of potential treatments.

摘要

目的

杏仁核功能理论是我们理解精神和神经发育障碍的核心。然而,对杏仁核的分子和细胞组成了解有限,阻碍了旨在开发新的治疗方法和干预措施的转化研究。本研究的目的是描述和比较杏仁核细胞的组成,以帮助弥合临床前模型与人类精神和神经发育障碍之间的差距。

方法

从多个人的杏仁核亚核(N=3,男性)和恒河猴(N=3,男性)中分离组织。进行单细胞 RNA 测序以描述单个核的转录组。

结果

结果显示,即使仅限于抑制性或兴奋性神经元,区域之间也存在很大的异质性。与先前的工作一致,数据突出了用于独特靶向特定细胞类型的单个标记基因的复杂性。跨物种分析表明,恒河猴模型非常适合理解人类杏仁核,但也存在局限性。例如,杏仁核腹外侧核(vLa)中的一个细胞簇在人类中比在恒河猴中更为丰富。此外,数据描述了具有紊乱相关基因相对富集的特定细胞簇。这些分析表明,人类丰富的 vLa 细胞簇与自闭症谱系障碍相关,可能突出了在最近的灵长类动物进化中出现的神经发育障碍的易感性。此外,表达中间细胞标志物的细胞簇富集了在人类全基因组关联研究中报道的与神经质、焦虑症和抑郁症相关的基因。

结论

总之,这些发现揭示了杏仁核的组成,并确定了特定的细胞类型,可以在基础科学研究中优先考虑,以更好地理解人类精神病理学并指导潜在治疗方法的开发。

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