Ontl T, Xing Y, Bai L, Kennedy E, Nelson S, Wakeman M, Magnusson K
Department of Biomedical Sciences, College of Veterinary Medicine and Biomedical Sciences, Program in Molecular, Cellular, and Integrative Neurosciences, Colorado State University, Fort Collins, CO 80523, USA.
Neuroscience. 2004;123(2):467-79. doi: 10.1016/j.neuroscience.2003.09.006.
The present study was designed to determine whether the changes that occur during aging in the expression of the N-methyl-D-aspartate (NMDA) receptor and two NMDA receptor subunits, zeta1 and epsilon2, are a continuation of developmental processes and whether protein and mRNA expression patterns of the subunits are similar across the lifespan. The prefrontal/frontal cortex of C57BL/6 mice of eight different ages (7-8, 13-15, 30-32, 49-53, and 70-72 days and 4.5, 11, and 25 months of age) were used to examine NMDA-displaceable [(3)H]glutamate binding and mRNA in tissue sections and mRNA and protein from homogenates. The lateral prefrontal/frontal cortex of C57BL/6 mice showed more significant declines in density of agonist binding to NMDA receptors during both development and aging than the medial cortex. Changes in mRNA expression for the epsilon2 subunit across the lifespan appeared to be related to the changes in NMDA receptor binding in the lateral cortex, even though the protein expression of the epsilon2 subunit did not show the same pattern of expression as the mRNA during development. The changes in epsilon2 subunit mRNA expression during adult aging may be a continuation of developmental processes, but there was also evidence that expression levels plateaued during early adulthood. The developmental expression of the zeta1subunit in the prefrontal/frontal cortex was influenced by gender and there was no significant effect of adult aging on either the protein or mRNA expression of this subunit. Determining how the expression of the NMDA receptor and its subunits change throughout the lifespan can help us to better understand the processes affecting the receptor during aging. These results should be useful for designing interventions into the aging process to repair or prevent changes in the NMDA receptor and its associated functions, such as learning and memory.
本研究旨在确定衰老过程中N-甲基-D-天冬氨酸(NMDA)受体及其两个亚基zeta1和epsilon2表达的变化是否是发育过程的延续,以及这些亚基的蛋白质和mRNA表达模式在整个生命周期中是否相似。使用八个不同年龄(7-8天、13-15天、30-32天、49-53天、70-72天以及4.5个月、11个月和25个月)的C57BL/6小鼠的前额叶/额叶皮质,来检测组织切片中NMDA可置换的[³H]谷氨酸结合和mRNA,以及匀浆中的mRNA和蛋白质。C57BL/6小鼠的外侧前额叶/额叶皮质在发育和衰老过程中,与内侧皮质相比,激动剂与NMDA受体结合的密度下降更为显著。尽管epsilon2亚基的蛋白质表达在发育过程中与mRNA的表达模式不同,但epsilon2亚基mRNA在整个生命周期中的表达变化似乎与外侧皮质中NMDA受体结合的变化有关。成年衰老过程中epsilon2亚基mRNA表达的变化可能是发育过程的延续,但也有证据表明其表达水平在成年早期趋于平稳。前额叶/额叶皮质中zeta1亚基的发育表达受性别影响,成年衰老对该亚基的蛋白质或mRNA表达均无显著影响。确定NMDA受体及其亚基在整个生命周期中的表达变化,有助于我们更好地理解衰老过程中影响该受体的机制。这些结果对于设计干预衰老过程的措施以修复或预防NMDA受体及其相关功能(如学习和记忆)的变化应该是有用的。