van Bockstaele E J, Commons K, Pickel V M
Department of Pathology, Anatomy, and Cell Biology, Jefferson Medical College of Thomas Jefferson University, Philadelphia, Pennsylvania 19107, USA.
J Comp Neurol. 1997 Dec 1;388(4):575-86. doi: 10.1002/(sici)1096-9861(19971201)388:4<575::aid-cne6>3.3.co;2-v.
The three classes of opioid receptors, mu, delta, and kappa, are distributed within the locus coeruleus (LC) of the rat brain. We have recently shown with immunoelectron microscopy that the mu-opioid receptor (muOR) is localized prominently to extrasynaptic sites on the plasma membranes of noradrenergic perikarya and dendrites of the LC. To further characterize the cellular distribution of other opioid receptors in this region, in this study, we examined the ultrastructural localization of an antipeptide sequence unique to the delta-opioid receptor (deltaOR) in sections that were also dual labeled for methionine-enkephalin (M-ENK), an opioid peptide known to be an endogenous ligand of the deltaOR. Immunoperoxidase labeling for deltaOR was localized primarily to the plasma membranes of presynaptic axon terminals and was also associated with large dense core vesicles. The deltaOR-labeled axon terminals formed both excitatory (asymmetric) and inhibitory (symmetric) type synaptic specializations with unlabeled dendrites and were frequently apposed by astrocytic processes. Dual labeling showed that, of 180 deltaOR-labeled axon terminals, 16% showed colocalization with M-ENK. These formed both types of synaptic junctions. Peroxidase labeling for deltaOR was also observed occasionally within dendrites, unmyelinated axons, and glial processes. The deltaOR-labeled dendrites were usually postsynaptic to unlabeled axon terminals that contained both small clear and large dense core vesicles. These results provide the first ultrastrucutral evidence that, in the LC, deltaOR may play a role in the presynaptic modulation of release of both excitatory and inhibitory neurotransmitters. They also suggest involvement of deltaOR in autoregulation of M-ENK release from axon terminals in this region.
阿片受体的三类,即μ、δ和κ受体,分布在大鼠脑的蓝斑(LC)内。我们最近通过免疫电子显微镜显示,μ-阿片受体(μOR)主要定位于蓝斑去甲肾上腺素能神经元胞体和树突质膜的突触外位点。为了进一步表征该区域其他阿片受体的细胞分布,在本研究中,我们在对甲硫氨酸脑啡肽(M-ENK,一种已知为δOR内源性配体的阿片肽)进行双重标记的切片中,检查了δ-阿片受体(δOR)特有的抗肽序列的超微结构定位。δOR的免疫过氧化物酶标记主要定位于突触前轴突终末的质膜,并且还与大的致密核心囊泡相关。δOR标记的轴突终末与未标记的树突形成兴奋性(不对称)和抑制性(对称)类型的突触特化,并且经常与星形胶质细胞的突起相邻。双重标记显示,在180个δOR标记的轴突终末中,16%显示与M-ENK共定位。这些形成了两种类型的突触连接。在树突、无髓轴突和神经胶质细胞突起中偶尔也观察到δOR的过氧化物酶标记。δOR标记的树突通常是含有小清亮囊泡和大致密核心囊泡的未标记轴突终末的突触后结构。这些结果提供了首个超微结构证据,表明在蓝斑中,δOR可能在兴奋性和抑制性神经递质释放的突触前调节中发挥作用。它们还表明δOR参与了该区域轴突终末M-ENK释放的自动调节。