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2
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μ-阿片受体(MOR1)在脑和脊髓中的分布与靶向作用。

Distribution and targeting of a mu-opioid receptor (MOR1) in brain and spinal cord.

作者信息

Arvidsson U, Riedl M, Chakrabarti S, Lee J H, Nakano A H, Dado R J, Loh H H, Law P Y, Wessendorf M W, Elde R

机构信息

Department of Cell Biology and Neuroanatomy, University of Minnesota, Minneapolis 55455, USA.

出版信息

J Neurosci. 1995 May;15(5 Pt 1):3328-41. doi: 10.1523/JNEUROSCI.15-05-03328.1995.

DOI:10.1523/JNEUROSCI.15-05-03328.1995
PMID:7751913
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6578209/
Abstract

Opioid receptors regulate neuronal activity by both pre- and postsynaptic mechanisms. We recently reported that the cloned delta-opioid receptor (DOR1) is primarily targeted to axons, suggesting a presynaptic role. In the present study we have studied the distribution and targeting of another opioid receptor, the mu-opioid receptor (MOR1), by raising anti-peptide antisera to the C-terminal peptide of MOR1. The specificity of the antisera was determined by analysis of transfected cells, Western blots, and immunoisolation studies. Immunohistochemistry showed that MOR1 immunoreactivity was enriched in many brain areas including cerebral cortex, striatum, hippocampus, locus coeruleus, and the superficial laminae of the dorsal horn. Moreover, MOR1-expressing neurons seem to target this receptor preferentially to their somatodendritic domain as determined by double-labeling experiments with MAP2. However, discrete populations of neurons target MOR1 to their axons, including some primary afferent neurons that express DOR1. In many regions enkephalin-containing axons were complementary to MOR1, suggesting by their proximity that enkephalins may be physiologically relevant ligands for this receptor. Thus, these results provide a morphological basis for understanding pre- and postsynaptic functions mediated by MOR1.

摘要

阿片受体通过突触前和突触后机制调节神经元活动。我们最近报道,克隆的δ-阿片受体(DOR1)主要定位于轴突,提示其具有突触前作用。在本研究中,我们通过制备针对MOR1 C末端肽的抗肽抗血清,研究了另一种阿片受体——μ-阿片受体(MOR1)的分布和靶向。通过对转染细胞、蛋白质免疫印迹和免疫分离研究的分析来确定抗血清的特异性。免疫组织化学显示,MOR1免疫反应性在许多脑区富集,包括大脑皮层、纹状体、海马、蓝斑和背角浅层。此外,通过与MAP2的双重标记实验确定,表达MOR1的神经元似乎将该受体优先靶向到其树突体区域。然而,离散的神经元群体将MOR1靶向到其轴突,包括一些表达DOR1的初级传入神经元。在许多区域,含脑啡肽的轴突与MOR1互补,通过它们的接近程度表明脑啡肽可能是该受体的生理相关配体。因此,这些结果为理解由MOR1介导的突触前和突触后功能提供了形态学基础。