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Kinetic modelling of the nitric oxide gradient generated in vitro by adherent cells expressing inducible nitric oxide synthase.

机译:通过表达诱导型一氧化氮合酶的贴壁细胞体外产生的一氧化氮梯度的动力学模型。

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摘要

Inducible nitric oxide (NO) synthase produces a long-lasting NO flux which can exert cytotoxic effects on target cells. A prerequisite for the understanding of the molecular basis of NO action is quantitative data on the availability of this small neutral radical molecule at both the spatial and temporal levels. The limits of NO availability depend on the respective rates of NO production, diffusion and autoxidation by molecular oxygen. Kinetic modeling of these processes has been performed for a widely used experimental system consisting of a monolayer of adherent cells cultured in vitro for hours in unstirred culture medium. It appears that: (i) the maximal NO concentration in the culture is in the immediate vicinity of the monolayer, where target cells will sediment; (ii) the steady-state NO concentration in this area is lower than 4 to 5 microM; and (iii) measurements of nitriteitrate or citrulline accumulation in the bulk cell medium culture during a given time period significantly underestimate (by a factor of up to 3 to 4) the true rate of NO synthesis at the level of the producer cell. This rate can be, nevertheless, easily estimated from the rate of production of the stable NO synthase products.
机译:诱导型一氧化氮(NO)合酶产生持久的NO通量,可对靶细胞产生细胞毒性作用。理解NO作用的分子基础的前提是有关这种小中性自由基分子在空间和时间水平上的可用性的定量数据。 NO可用性的极限取决于分子氧产生,扩散和自氧化的NO各自的速率。这些过程的动力学模型已针对广泛使用的实验系统进行了动力学建模,该系统由单层贴壁细胞组成,这些细胞在未搅拌的培养基中体外培养了数小时。似乎:(i)培养物中最大的NO浓度在单层的紧邻区域,靶细胞将在那里沉积; (ii)该区域的稳态NO浓度低于4至5 microM; (iii)在给定时间内测量散装细胞培养基中亚硝酸盐/硝酸盐或瓜氨酸的积累,大大低估了生产细胞水平上NO合成的真实速率(最高达3-4倍)。然而,可以从稳定的NO合酶产物的生产速率容易地估计该速率。

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