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Quantitative fluorescence microscopy provides high resolution imaging of passive diffusion and P-gp mediated efflux at the in vivo blood–brain barrier

机译:定量荧光显微镜可提供体内血脑屏障被动扩散和P-gp介导外排的高分辨率成像

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摘要

Quantitative fluorescent microscopy is an emerging technology that has provided significant insight into cellular dye accumulation, organelle function, and tissue physiology. However, historically dyes have only been used to qualitatively or semi-quantitatively (fold change) determine changes in blood–brain barrier (BBB) integrity. Herein, we present a novel method to calculate the blood to brain transfer rates of the dyes rhodamine 123 and Texas red across the in situ BBB. We observed that rhodamine 123 is subject to p-glycoprotein mediated efflux at the rat BBB and can be increased nearly 20-fold with p-glycoprotein inhibition. However, Texas Red appears to not be subject to MRP2 mediated efflux at the rat BBB, agreeing with literature reports suggesting MRP2 may lack functionality at the normal rat BBB. Lastly, we present data demonstrating that once dyes have crossed the BBB, diffusion of the dye molecule is not as instantaneous as has been previously suggested. We propose that future work can now be completed to (1) match BBB transfer coefficients to interstitial diffusion constants and (2) use dyes with specific affinities to cellular organelles or that have specific properties (e.g., subject to efflux transporters) to more fully understand BBB physiology.
机译:定量荧光显微镜技术是一种新兴技术,已为细胞染料积累,细胞器功能和组织生理学提供了重要见识。但是,从历史上看,染料仅用于定性或半定量(倍数变化)来确定血脑屏障(BBB)完整性的变化。本文中,我们提出了一种新颖的方法来计算染料若丹明123和德克萨斯红在原位BBB上的血液向大脑的转移速率。我们观察到若丹明123在大鼠BBB处受到p-糖蛋白介导的流出,并且可以通过p-糖蛋白抑制作用增加近20倍。但是,德克萨斯红似乎不在大鼠BBB处受到MRP2介导的流出,与文献报道表明MRP2在正常大鼠BBB处可能缺乏功能相一致。最后,我们提供的数据表明,一旦染料穿过BBB,染料分子的扩散就不会像以前所建议的那样瞬时。我们建议现在可以完成以下工作:(1)使BBB转移系数与间隙扩散常数相匹配;(2)使用对细胞器具有特定亲和力或具有特定特性(例如,受外排转运蛋白影响)的染料,以更充分地理解BBB生理学。

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