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利用实时定量聚合酶链反应鉴定海马锥体神经元和 CA1 辐射层中间神经元亚型中的内源性大麻素生物合成酶的 mRNA。

Identification of mRNA for endocannabinoid biosynthetic enzymes within hippocampal pyramidal cells and CA1 stratum radiatum interneuron subtypes using quantitative real-time polymerase chain reaction.

机构信息

Brigham Young University, Department of Physiology and Developmental Biology, Provo, UT 84602, USA.

出版信息

Neuroscience. 2012 Aug 30;218:89-99. doi: 10.1016/j.neuroscience.2012.05.012. Epub 2012 May 17.

DOI:10.1016/j.neuroscience.2012.05.012
PMID:22609938
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3409849/
Abstract

The hippocampus is required for short-term memory and contains both excitatory pyramidal cells and inhibitory interneurons. These cells exhibit various forms of synaptic plasticity, the mechanism underlying learning and memory. More recently, endocannabinoids were identified to be involved in synaptic plasticity. Our goal was to describe the distribution of endocannabinoid biosynthetic enzymes within CA1 stratum radiatum interneurons and CA3/CA1 pyramidal cells. We extracted mRNA from single interneurons and pyramidal cells and used real-time quantitative polymerase chain reaction (RT-PCR) to detect the presence of 12-lipoxygenase, N-acyl-phosphatidylethanolamine-specific phospholipase D, diacylglycerol lipase α, and type I metabotropic glutamate receptors, all known to be involved in endocannabinoid production and plasticity. We observed that the expression of endocannabinoid biosynthetic enzyme mRNA does occur within interneurons and that it is coexpressed with type I metabotropic glutamate receptors, suggesting interneurons have the potential to produce endocannabinoids. We also identified that CA3 and CA1 pyramidal cells express endocannabinoid biosynthetic enzyme mRNA. Our data provide the first molecular biological evidence for putative endocannabinoid production in interneurons, suggesting their potential ability to regulate endocannabinoid-mediated processes, such as synaptic plasticity.

摘要

海马体是短期记忆所必需的,其中包含兴奋性锥体神经元和抑制性中间神经元。这些细胞表现出各种形式的突触可塑性,这是学习和记忆的基础。最近,内源性大麻素被确定参与突触可塑性。我们的目标是描述内源性大麻素生物合成酶在 CA1 辐射层中间神经元和 CA3/CA1 锥体神经元中的分布。我们从单个中间神经元和锥体神经元中提取 mRNA,并使用实时定量聚合酶链反应 (RT-PCR) 检测 12-脂氧合酶、N-酰基-磷酸乙醇胺特异性磷脂酶 D、二酰基甘油脂肪酶 α 和 I 型代谢型谷氨酸受体的存在,所有这些都已知参与内源性大麻素的产生和可塑性。我们观察到内源性大麻素生物合成酶 mRNA 的表达确实发生在中间神经元中,并且与 I 型代谢型谷氨酸受体共表达,这表明中间神经元具有产生内源性大麻素的潜力。我们还确定 CA3 和 CA1 锥体细胞表达内源性大麻素生物合成酶 mRNA。我们的数据为中间神经元中内源性大麻素产生的潜在可能性提供了第一个分子生物学证据,表明它们可能具有调节内源性大麻素介导的过程(如突触可塑性)的能力。

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