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首页> 外文期刊>The Journal of Neuroscience: The Official Journal of the Society for Neuroscience >Ultrastructural immunolabeling shows prominent presynaptic vesicular localization of delta-opioid receptor within both enkephalin- and nonenkephalin-containing axon terminals in the superficial layers of the rat cervical spinal cord.
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Ultrastructural immunolabeling shows prominent presynaptic vesicular localization of delta-opioid receptor within both enkephalin- and nonenkephalin-containing axon terminals in the superficial layers of the rat cervical spinal cord.

机译:超微结构免疫标记显示大鼠颈脊髓表层的脑啡肽和非脑啡肽的轴突末端内的δ-阿片样物质突触前囊泡局部定位。

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摘要

Opioid peptides, Met5- and Leu5-enkephalin, are known endogenous ligands for the delta-opioid receptor (DOR) associated with opioid analgesia at the spinal level. To determine the cellular sites for DOR-mediated actions, we examined the ultrastructural localization of DOR and Met5-enkephalin (ME) in the spinal cord by combining immunoperoxidase and immunogold-silver labeling for antibodies against DOR and ME, respectively. Antibodies for DOR localization were raised in guinea pig against peptide 34-47 (p34), an amino acid sequence within the extracellular N-terminus of the DOR recently cloned from mouse neuroblastoma glioma (NG-108) cells. Selective immunoperoxidase labeling for DOR was detected by light microscopy in NG-108 cells and in the lamina I and II of the dorsal horn of the spinal cord (C2-C4). Electron microscopy of these spinal laminae revealed that the majority of the punctate varicosities seen by light microscopy were axon terminals. delta-opioid receptor-like immunoreactivity (DOR-LI) in axon terminals was most prominently associated with large dense core vesicles, and sometimes seen along the membranes of small clear vesicles and segments of the plasmalemma. A semiquantitative analysis of dually labeled sections revealed that of the terminals showing DOR-LI, 23/102 (23%) also contained Met5-enkephalin-like immunoreactivity (ME-LI). Conversely, 23/35 (66%) of the terminals showing ME-LI also showed DOR-LI. In addition to the presynaptic localization, selective postsynaptic densities within dendrites were also occasionally (9%) immunolabeled for the opioid receptor. These results provide the first ultrastructural evidence that DOR may serve autoreceptor functions on ME terminals as well as presynaptic modulation of other transmitters in the dorsal horn of the rat spinal cord. Additionally, the vesicular localization of DOR-LI in axon terminals suggests the involvement of these organelles in the transport of the receptors to the plasma membrane.
机译:阿片肽Met5-和Leu5-脑啡肽是已知的与脊髓水平的阿片类药物镇痛有关的δ-阿片受体(DOR)的内源性配体。为了确定DOR介导的作用的细胞位点,我们通过结合针对DOR和ME的免疫过氧化物酶和免疫金银标记分别检查了DOR和Met5-脑啡肽(ME)在脊髓中的超微结构定位。在豚鼠中产生了针对肽34-47(p34)的DOR定位抗体,肽34-47(p34)是最近从小鼠神经母细胞胶质瘤(NG-108)细胞克隆的DOR胞外N端的氨基酸序列。通过光学显微镜在NG-108细胞以及脊髓背角(C2-C4)的层板I和II中检测到DOR的选择性免疫过氧化物酶标记。这些脊髓层的电子显微镜检查显示,通过光学显微镜观察到的大多数点状静脉曲张都是轴突末端。轴突末端的类阿片受体样免疫反应性(DOR-LI)与大型密集的核心囊泡最显着相关,有时在小的透明囊泡膜和浆膜节段可见。双重标记切片的半定量分析显示,显示DOR-LI的末端23/102(23%)也包含Met5-脑啡肽样免疫反应性(ME-LI)。相反,显示ME-LI的终端中有23/35(66%)也显示DOR-LI。除了突触前的定位外,树突内选择性的突触后密度也偶尔被阿片受体免疫标记(9%)。这些结果提供了第一个超微结构证据,即DOR可能在ME末端发挥自动受体功能,并在大鼠脊髓背角中对其他递质进行突触前调制。另外,DOR-LI在轴突末端的囊泡定位表明这些细胞器参与受体向质膜的转运。

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