Law Amanda J, Weickert Cynthia Shannon, Webster Maree J, Herman Mary M, Kleinman Joel E, Harrison Paul J
Department of Psychiatry, University of Oxford, Neurosciences Building, Warneford Hospital, Oxford OX3 7JX, UK.
Eur J Neurosci. 2003 Sep;18(5):1197-205. doi: 10.1046/j.1460-9568.2003.02850.x.
The N-methyl-d-aspartate receptor plays a critical role in the formation and maintenance of synapses during brain development. In the rodent, changes in subunit expression and assembly of the heteromeric receptor complex accompany these maturational processes. However, little is known about N-methyl-d-aspartate receptor subunit expression during human brain development. We used in situ hybridization to examine the distribution and relative abundance of NR1, NR2A and NR2B subunit messenger ribonucleic acids in the hippocampal formation and adjacent cortex of 34 human subjects at five stages of life (neonate, infant, adolescent, young adult and adult). At all ages, the three messenger ribonucleic acids were expressed in all subfields, predominantly by pyramidal neurons, granule cells and polymorphic hilar cells. However, their abundance varied across ontogeny. Levels of NR1 messenger ribonucleic acid in CA4, CA3 and CA2 subfields were significantly lower in the neonate than all other age groups. In the dentate gyrus, subiculum and parahippocampal gyrus, NR2B messenger ribonucleic acid levels were higher in the neonate than in older age groups. NR2A messenger ribonucleic acid levels remained constant, leading to an age-related increase in NR2A/2B transcript ratio. We conclude that N-methyl-d-aspartate receptor subunit messenger ribonucleic acids are differentially expressed during postnatal development of the human hippocampus, with a pattern similar but not identical to that seen in the rodent. Changes in subunit composition may thus contribute to maturational differences in human hippocampal N-methyl-d-aspartate receptor function, and to their role in the pathophysiology of schizophrenia and other neurodevelopmental disorders.
N-甲基-D-天冬氨酸受体在大脑发育过程中对突触的形成和维持起着关键作用。在啮齿动物中,异聚体受体复合物的亚基表达和组装变化伴随着这些成熟过程。然而,关于人类大脑发育过程中N-甲基-D-天冬氨酸受体亚基的表达情况却知之甚少。我们采用原位杂交技术,检测了34名处于五个生命阶段(新生儿、婴儿、青少年、青年和成年人)的人类受试者海马结构及相邻皮质中NR1、NR2A和NR2B亚基信使核糖核酸的分布和相对丰度。在所有年龄段,这三种信使核糖核酸在所有亚区均有表达,主要由锥体细胞、颗粒细胞和多形性门区细胞表达。然而,它们的丰度在个体发育过程中有所不同。CA4、CA3和CA2亚区的NR1信使核糖核酸水平在新生儿中显著低于所有其他年龄组。在齿状回、海马下托和海马旁回中,新生儿的NR2B信使核糖核酸水平高于年龄较大的组。NR2A信使核糖核酸水平保持恒定,导致NR2A/2B转录本比率随年龄增加。我们得出结论,N-甲基-D-天冬氨酸受体亚基信使核糖核酸在人类海马体出生后的发育过程中存在差异表达,其模式与啮齿动物相似但不完全相同。因此,亚基组成的变化可能导致人类海马体N-甲基-D-天冬氨酸受体功能的成熟差异,以及它们在精神分裂症和其他神经发育障碍病理生理学中的作用。