Establishment of the deuterium oxide dilution method as a new possibility for determining the transendothelial water permeability.

IF 2.9 4区 医学 Q2 PHYSIOLOGY
Hannes Müller, Janina Hahn, Angelina Gierke, Robert Stark, Cornelia Brunner, Thomas K Hoffmann, Jens Greve, Oliver Wittekindt, Robin Lochbaum
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Abstract

Increase in transendothelial water permeability is an essential etiological factor in a variety of diseases like edema and shock. Despite the high clinical relevance, there has been no precise method to detect transendothelial water flow until now. The deuterium oxide (D2O) dilution method, already established for measuring transepithelial water transport, was used to precisely determine the transendothelial water permeability. It detected appropriate transendothelial water flow induced by different hydrostatic forces. This was shown in four different endothelial cell types. The general experimental setup was verified by gravimetry and absorbance spectroscopy. Determination of transendothelial electrical resistance (TEER) and immunocytochemical staining for proteins of the cell-cell contacts were performed to ensure that no damage to the endothelium occurred because of the measurements. Furthermore, endothelial barrier function was modulated. Measurement of transendothelial water flux was verified by measuring the TEER, the apparent permeability coefficient and the electrical capacity. The barrier-promoting substances cyclic adenosine monophosphate and iloprost reduced TEER and electrical capacity and increased permeability. This was accompanied by a reduced transendothelial water flux. In contrast, the barrier-damaging substances thrombin, histamine and bradykinin reduced TEER and electrical capacity, but increased permeability. Here, an increased water flow was shown. This newly established in vitro method for direct measurement of transendothelial water permeability was verified as a highly precise technique in various assays. The use of patient-specific endothelial cells enables individualized precision medicine in the context of basic edema research, for example regarding the development of barrier-protective pharmaceuticals.

将氧化氘稀释法作为测定跨内皮透水性的一种新方法。
跨内皮水渗透性增加是水肿和休克等多种疾病的重要病因。尽管具有高度的临床意义,但迄今为止还没有一种精确的方法来检测跨内皮水流。氧化氘(D2O)稀释法已经用于测量经上皮细胞的水运输,我们采用这种方法来精确测定经内皮细胞的水渗透性。它能检测到不同静水压引起的适当的跨内皮水流。这在四种不同类型的内皮细胞中得到了证明。重力测量法和吸光度光谱法对一般实验装置进行了验证。还测定了跨内皮电阻(TEER),并对细胞-细胞接触处的蛋白质进行了免疫细胞化学染色,以确保测量不会对内皮造成损伤。此外,还对内皮屏障功能进行了调节。通过测量 TEER、表观渗透系数和电容量,验证了跨内皮水通量的测量结果。促进屏障的物质环磷酸腺苷和伊洛前列素降低了 TEER 和电容量,增加了渗透性。与此同时,跨内皮水通量也减少了。相反,破坏屏障的物质凝血酶、组胺和缓激肽会降低 TEER 和电容量,但会增加渗透性。这里显示的是水流量的增加。这种新建立的体外直接测量跨内皮透水性的方法在各种试验中被证实是一种高度精确的技术。使用患者特异性内皮细胞可以在水肿基础研究中实现个体化精准医疗,例如开发屏障保护药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
8.80
自引率
2.20%
发文量
121
审稿时长
4-8 weeks
期刊介绍: Pflügers Archiv European Journal of Physiology publishes those results of original research that are seen as advancing the physiological sciences, especially those providing mechanistic insights into physiological functions at the molecular and cellular level, and clearly conveying a physiological message. Submissions are encouraged that deal with the evaluation of molecular and cellular mechanisms of disease, ideally resulting in translational research. Purely descriptive papers covering applied physiology or clinical papers will be excluded. Papers on methodological topics will be considered if they contribute to the development of novel tools for further investigation of (patho)physiological mechanisms.
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