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昼夜节律钟调节小鼠和人细胞的血脑屏障外排。

A circadian clock regulates efflux by the blood-brain barrier in mice and human cells.

机构信息

Chronobiology and Sleep Institute, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.

Howard Hughes Medical Institute, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.

出版信息

Nat Commun. 2021 Jan 27;12(1):617. doi: 10.1038/s41467-020-20795-9.

Abstract

The blood-brain barrier (BBB) is critical for neural function. We report here circadian regulation of the BBB in mammals. Efflux of xenobiotics by the BBB oscillates in mice, with highest levels during the active phase and lowest during the resting phase. This oscillation is abrogated in circadian clock mutants. To elucidate mechanisms of circadian regulation, we profiled the transcriptome of brain endothelial cells; interestingly, we detected limited circadian regulation of transcription, with no evident oscillations in efflux transporters. We recapitulated the cycling of xenobiotic efflux using a human microvascular endothelial cell line to find that the molecular clock drives cycling of intracellular magnesium through transcriptional regulation of TRPM7, which appears to contribute to the rhythm in efflux. Our findings suggest that considering circadian regulation may be important when therapeutically targeting efflux transporter substrates to the CNS.

摘要

血脑屏障(BBB)对神经功能至关重要。我们在此报告哺乳动物的 BBB 昼夜节律调节。在小鼠中,BBB 对外来物质的排出呈振荡性,在活动期最高,在休息期最低。这种振荡在生物钟突变体中被消除。为了阐明昼夜节律调节的机制,我们对脑内皮细胞的转录组进行了分析;有趣的是,我们检测到转录的昼夜节律调节有限,外排转运体没有明显的振荡。我们使用人微血管内皮细胞系重现了外排的循环,发现分子钟通过 TRPM7 的转录调节驱动细胞内镁的循环,这似乎有助于外排的节律。我们的研究结果表明,当治疗性地将外排转运体的底物靶向中枢神经系统时,考虑昼夜节律调节可能很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f5e/7841146/83e7864dbb15/41467_2020_20795_Fig1_HTML.jpg

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