Zhu Y, Hsu M S, Pintar J E
Department of Neuroscience and Cell Biology, University of Medicine and Dentistry of New Jersey-Robert Wood Johnson Medical School, Piscataway, New Jersey 08854, USA.
J Neurosci. 1998 Apr 1;18(7):2538-49. doi: 10.1523/JNEUROSCI.18-07-02538.1998.
To characterize further the establishment of the opioid system during prenatal mouse development, we have examined the spatial and temporal expression patterns of mu, kappa, and delta opioid receptor mRNAs and find that the expression patterns of these mRNAs are distinct at all ages. Within the embryo, kappa is the first opioid receptor expressed, with transcripts detected in the gut epithelium as early as embryonic day 9.5 (E9.5). By E10.5, mu receptor expression is first detected in the facial-vestibulocochlear preganglion complex, whereas delta receptor mRNA is first detected at E12.5 in several peripheral tissues, including the olfactory epithelium, heart, limb bud, and tooth. In the brain, both mu and kappa mRNAs are first detected at E11.5 in the basal ganglia and midbrain, respectively. During mid-gestation and late gestation, the expression of both mu and kappa receptors extends to other brain regions that exhibit high expression in the adult, including the medial habenula, hypothalamus, pons, and medulla for mu and the basal ganglia, thalamus, hypothalamus, raphe, and ventral tegmental area for kappa. Thus by E17.5, many aspects of the adult expression patterns of mu and kappa receptors already have been established. Compared with mu and kappa, delta receptor mRNA expression in the brain begins relatively late, and the expression levels remain very low even at E19.5. In contrast to its late appearance in the brain, however, delta is the first opioid receptor expressed in the dorsal root ganglion, at E12.5, before its expression in the spinal cord begins at E15.5. Mu receptor is the first opioid receptor expressed in the spinal cord, at E11.5. These results extend previous ligand-binding data to significantly earlier ages and suggest that early developmental events in both neural and non-neural tissues may be modulated by opioid receptors. Several examples of possible autocrine and paracrine loops of opioid peptide and receptor expression have been identified, suggesting a role for these local circuits in developmental processes.
为了进一步描述产前小鼠发育过程中阿片系统的建立,我们研究了μ、κ和δ阿片受体mRNA的时空表达模式,发现这些mRNA的表达模式在所有年龄段都不同。在胚胎内,κ是最早表达的阿片受体,早在胚胎第9.5天(E9.5)就在肠道上皮中检测到转录本。到E10.5时,首次在面-前庭蜗神经节前复合体中检测到μ受体表达,而δ受体mRNA最早在E12.5时在包括嗅觉上皮、心脏、肢芽和牙齿在内的几个外周组织中检测到。在大脑中,μ和κ mRNA分别最早在E11.5时在基底神经节和中脑中检测到。在妊娠中期和晚期,μ和κ受体的表达扩展到成年期高表达的其他脑区,μ受体包括内侧缰核、下丘脑、脑桥和延髓,κ受体包括基底神经节、丘脑、下丘脑、中缝和腹侧被盖区。因此,到E17.5时,μ和κ受体的成年表达模式的许多方面已经建立。与μ和κ相比,δ受体mRNA在大脑中的表达开始相对较晚,即使在E19.5时表达水平仍非常低。然而,与它在大脑中出现较晚相反,δ是背根神经节中最早表达的阿片受体,在E12.5时表达,早于其在E15.5时在脊髓中的表达开始。μ受体是脊髓中最早表达的阿片受体,在E11.5时表达。这些结果将先前的配体结合数据扩展到显著更早的年龄,并表明神经和非神经组织中的早期发育事件可能受到阿片受体的调节。已经确定了阿片肽和受体表达的几个可能的自分泌和旁分泌回路实例,表明这些局部回路在发育过程中起作用。