Wada Yukiyo, Inoko Masaki, Ishihara Kanako, Fukumoto Karin, Tsurudome Yuya, Horiguchi Michiko, Fujimura Akio, Ushijima Kentaro
Division of Pharmaceutics, Faculty of Pharmaceutical Sciences, Sanyo-Onoda City University, Yamaguchi 756-0884, Japan.
Department of Pharmaceutical Engineering, Sanyo-Onoda City University, Yamaguchi 756-0884, Japan.
Pharmaceuticals (Basel). 2025 Jan 30;18(2):191. doi: 10.3390/ph18020191.
ATP-binding cassette (ABC) transporters are expressed in the vascular walls of brain capillaries and remove toxic chemicals from the brain. The expression of ABC transporters in peripheral organs is transcriptionally regulated by clock genes and exhibits 24 h periodic fluctuations. In addition, clock gene outputs diminish with aging. In this study, we evaluated whether the expression of ABC transporters in the blood-brain barrier (BBB) of young mice had a 24 h cycle, and whether the expression of ABC transporters in the BBB decreased with age. Brain microvascular (BMV) fractions from the cerebral cortex of male C57BL/6J mice were prepared using dextran. BMV fractions from young mice (12 weeks old) were prepared every four hours to evaluate 24 h rhythmicity. BMV fractions from both young and aged mice (85 weeks old) were prepared when protein expression peaked (Zeitgeber Time 5). Protein and mRNA expression of ABC transporters in BMV fractions were measured. In young mice, protein expression of P-glycoprotein, breast cancer resistance protein, and multidrug resistance protein 4 showed time-dependent variations with a peak in the light phase (Zeitgeber Time 5); mRNA expression showed no time-dependent variation. The protein expression of these transporters was lower in the BBB of aged mice than in that of young mice, although mRNA expression did not differ between young and aged mice. ABC transporter protein expression levels in BMV endothelial cells decreased with aging; however, mRNA levels did not change, which suggests changes in protein expression did not result from diminished clock gene output. Further studies are needed to elucidate the mechanisms by which ABC transporter expression in the BBB decreases with aging.
ATP结合盒(ABC)转运蛋白在脑毛细血管的血管壁中表达,并从大脑中清除有毒化学物质。ABC转运蛋白在外周器官中的表达受生物钟基因转录调控,并呈现24小时的周期性波动。此外,生物钟基因的输出随衰老而减少。在本研究中,我们评估了幼鼠血脑屏障(BBB)中ABC转运蛋白的表达是否具有24小时周期,以及BBB中ABC转运蛋白的表达是否随年龄增长而降低。使用葡聚糖制备雄性C57BL/6J小鼠大脑皮质的脑微血管(BMV)组分。每4小时制备一次幼鼠(12周龄)的BMV组分,以评估24小时节律性。在蛋白质表达达到峰值时(授时时间5),制备幼鼠和老年鼠(85周龄)的BMV组分。测量BMV组分中ABC转运蛋白的蛋白质和mRNA表达。在幼鼠中,P-糖蛋白、乳腺癌耐药蛋白和多药耐药蛋白4的蛋白质表达呈现时间依赖性变化,在光照期达到峰值(授时时间5);mRNA表达未显示时间依赖性变化。尽管幼鼠和老年鼠之间的mRNA表达没有差异,但这些转运蛋白的蛋白质表达在老年鼠的BBB中低于幼鼠。BMV内皮细胞中ABC转运蛋白的蛋白质表达水平随衰老而降低;然而,mRNA水平没有变化,这表明蛋白质表达的变化并非由生物钟基因输出减少所致。需要进一步研究以阐明BBB中ABC转运蛋白表达随衰老而降低的机制。