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Corticotropin-releasing factor in the mouse central nucleus of the amygdala: Ultrastructural distribution in NMDA-NR1 receptor subunit expressing neurons as well as projection neurons to the bed nucleus of the stria terminalis

机译:在杏仁达拉的小鼠中央核中释放因子:NMDA-NR1受体亚单位的超微结构分布表达神经元的神经元突出神经元的脉络态

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摘要

Corticotropin-releasing factor (CRF) and glutamate are critical signaling molecules in the central nucleus of the amygdala (CeA). Central amygdala CRF, acting via the CRF type 1 receptor (CRF-R1), plays an integral role in stress responses and emotional learning, processes that are generally known to involve functional NMDA-type glutamate receptors. There is also evidence that CRF expressing CeA projection neurons to the bed nucleus of the stria terminalis (BNST) play an important role in stress related behaviors. Despite the potentially significant interactions between CRF and NMDA receptors in the CeA, the synaptic organization of these systems is largely unknown. Using dual labeling high resolution immunocytochemical electron microscopy, it was found that individual somata and dendrites displayed immunoreactivity for CRF and the NMDA-NR1 (NR1) subunit in the mouse CeA. In addition, CRF-containing axon terminals contacted postsynaptic targets in the CeA, some of which also expressed NR1. Neuronal profiles expressing the CRF type 1 receptor (CRF-R1), identified by the expression of green fluorescent protein (GFP) in bacterial artificial chromosome (BAC) transgenic mice, also contained NR1, and GFP immunoreactive terminals formed synapses with NR1 containing dendrites. Although CRF and GFP were only occasionally co-expressed in individual somata and dendritic profiles, contacts between labeled axon terminals and dendrites were frequently observed. A combination of tract tracing and immunocytochemistry revealed that a population of CeA CRF neurons projected to the BNST. It was also found that CRF, or GFP expressing terminals directly contacted CeA-BNST projection neurons. These results indicate that the NMDA receptor is positioned for the postsynaptic regulation of CRF expressing CeA neurons and the modulation of signals conveyed by CRF inputs. Interactions between CRF and NMDA receptor mediated signaling in CeA neurons, including those projecting to the BNST, may provide the synaptic basis for integrating the experience of stress and relevant environmental stimuli with behaviors that may be of particular relevance to stress-related learning and the emergence of psychiatric disorders, including drug addiction.
机译:促肾上腺皮质激素释放因子(CRF)和谷氨酸是杏仁核(CeA)中央核中的关键信号分子。中央杏仁核CRF通过1型CRF受体(CRF-R1)发挥作用,在应激反应和情绪学习中起着不可或缺的作用,这些过程通常已知涉及功能性NMDA型谷氨酸受体。也有证据表明,表达CRF的CeA投射神经元向纹状体终末床核(BNST)的表达在应激相关行为中起重要作用。尽管在CeA中CRF和NMDA受体之间可能存在潜在的显着相互作用,但这些系统的突触组织很大程度上未知。使用双标记高分辨率免疫细胞化学电子显微镜,发现单个的躯体和树突对小鼠CeA中的CRF和NMDA-NR1(NR1)亚基表现出免疫反应性。此外,含有CRF的轴突末端接触CeA中的突触后靶标,其中一些也表达NR1。通过细菌人工染色体(BAC)转基因小鼠中绿色荧光蛋白(GFP)的表达鉴定出的表达CRF 1型受体(CRF-R1)的神经元特征也包含NR1,并且GFP免疫反应性末端与含有NR1的树突形成了突触。尽管CRF和GFP仅在个别的躯体和树突状结构中偶尔共表达,但经常观察到标记的轴突末端与树突状结构之间的接触。道追踪和免疫细胞化学的组合显示,CeA CRF神经元的群体投射到BNST。还发现,CRF或GFP表达末端直接接触CeA-BNST投射神经元。这些结果表明,NMDA受体定位于表达CRF的CeA神经元的突触后调节和由CRF输入传递的信号的调节。 CRF和NMDA受体介导的CeA神经元信号传导之间的相互作用,包括投射到BNST的相互作用,可能为整合压力和相关环境刺激的经验与可能与压力相关的学习和出现特别相关的行为提供突触基础。精神疾病,包括吸毒成瘾。

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