Department of Psychiatry, University of Wisconsin-Madison, Madison, Wisconsin; Neuroscience Training Program, University of Wisconsin-Madison, Madison, Wisconsin; HealthEmotions Research Institute, University of Wisconsin-Madison, Madison, Wisconsin.
Department of Cell Biology, State University of New York Downstate Medical Center, Brooklyn, New York.
Biol Psychiatry. 2020 Oct 15;88(8):638-648. doi: 10.1016/j.biopsych.2020.05.009. Epub 2020 May 19.
Children exhibiting extreme anxious temperament (AT) are at an increased risk for developing anxiety and depression. Our previous mechanistic and neuroimaging work in young rhesus monkeys linked the central nucleus of the amygdala to AT and its underlying neural circuit.
Here, we used laser capture microscopy and RNA sequencing in 47 young rhesus monkeys to investigate AT's molecular underpinnings by focusing on neurons from the lateral division of the central nucleus of the amygdala (CeL). RNA sequencing identified numerous AT-related CeL transcripts, and we used immunofluorescence (n = 3) and tract-tracing (n = 2) methods in a different sample of monkeys to examine the expression, distribution, and projection pattern of neurons expressing one of these transcripts.
We found 555 AT-related transcripts, 14 of which were confirmed with high statistical confidence (false discovery rate < .10), including protein kinase C delta (PKCδ), a CeL microcircuit cell marker implicated in rodent threat processing. We characterized PKCδ neurons in the rhesus CeL, compared its distribution with that of the mouse, and demonstrated that a subset of these neurons project to the laterodorsal bed nucleus of the stria terminalis.
These findings demonstrate that CeL PKCδ is associated with primate anxiety, provides evidence of a CeL to laterodorsal bed nucleus of the stria terminalis circuit that may be relevant to understanding human anxiety, and points to specific molecules within this circuit that could serve as potential treatment targets for anxiety disorders.
表现出极度焦虑气质(AT)的儿童患焦虑症和抑郁症的风险增加。我们之前在幼年恒河猴中的机制和神经影像学研究将杏仁核中央核与 AT 及其潜在的神经回路联系起来。
在这里,我们使用激光捕获显微镜和 RNA 测序技术在 47 只年轻的恒河猴中,通过关注杏仁核中央核的外侧部分(CeL)的神经元,研究 AT 的分子基础。RNA 测序确定了许多与 AT 相关的 CeL 转录本,我们使用免疫荧光(n=3)和追踪(n=2)方法在另一批猴子中检查了表达这些转录本之一的神经元的表达、分布和投射模式。
我们发现了 555 个与 AT 相关的转录本,其中 14 个具有很高的统计置信度(错误发现率<.10),包括蛋白激酶 C 三角洲(PKCδ),这是一种与啮齿动物威胁处理有关的 CeL 微电路细胞标记物。我们在恒河猴 CeL 中描述了 PKCδ 神经元,比较了其与小鼠的分布,并证明了这些神经元的一部分投射到终纹床核的背外侧核。
这些发现表明 CeL PKCδ 与灵长类动物的焦虑有关,为 CeL 到终纹床核的背外侧核的回路提供了证据,这可能与理解人类焦虑有关,并指出了该回路中可能作为焦虑症潜在治疗靶点的特定分子。