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渗透梯度刺激下脊椎动物肝细胞的容积反应:一种理论方法。

Volumetric response of vertebrate hepatocytes challenged by osmotic gradients: a theoretical approach.

作者信息

Espelt M V, Alleva K, Amodeo G, Krumschnabel G, Rossi R C, Schwarzbaum P J

机构信息

Instituto de Química y Fisicoquímica Biológicas (Facultad de Farmacia y Bioquímica), Universidad de Buenos Aires, C1113AAD Buenos Aires, Argentina.

出版信息

Comp Biochem Physiol B Biochem Mol Biol. 2008 May;150(1):103-11. doi: 10.1016/j.cbpb.2008.02.001. Epub 2008 Feb 9.

Abstract

In this study we use a theoretical approach to study the volumetric response of goldfish hepatocytes challenged by osmotic gradients and compared it with that of hepatocytes from another teleost (the trout) and a mammal (the rat). Particular focus was given to the multiple non-linear interactions of transport systems enabling hypotonically challenged cells to trigger a compensatory response known as volume regulatory decrease or RVD. For this purpose we employed a mathematical model which describes the rates of change of the intracellular concentrations of main diffusible ions, of the cell volume, and of the membrane potential. The model was fitted to experimental data on the kinetics of volume change of hepatocytes challenged by anisotonic media. In trout and rat hepatocytes, experimental results had shown that hypotonic cell swelling was followed by RVD, whereas goldfish cells swelled with no concomitant RVD (M.V. Espelt et al., 2003, J. Exp. Biol. 206, 513-522). A comparison between data predicted by the model and that obtained experimentally suggests that in trout and rat hepatocytes hypotonicity activates a sensor element and this, in turn, activates an otherwise silent efflux of KCl - whose kinetics could be successfully predicted - thereby leading to volume down-regulation. In contrast, with regard to the absence of RVD in goldfish hepatocytes the model proposed suggests that either a sensor element triggering RVD is absent or that the effector mechanism (the loss of KCl) remains inactive under the conditions employed. In line with this, we recently found that extracellular nucleotides may be required to induce RVD in these cells, indicating that our model could indeed lead to useful predictions.

摘要

在本研究中,我们采用理论方法来研究金鱼肝细胞在渗透压梯度刺激下的容积反应,并将其与另一种硬骨鱼(鳟鱼)和一种哺乳动物(大鼠)的肝细胞的容积反应进行比较。特别关注了转运系统的多种非线性相互作用,这些相互作用使受到低渗刺激的细胞能够触发一种称为容积调节性降低(RVD)的补偿反应。为此,我们采用了一个数学模型,该模型描述了主要可扩散离子的细胞内浓度、细胞容积和膜电位的变化速率。该模型与等渗介质刺激下肝细胞容积变化动力学的实验数据进行了拟合。在鳟鱼和大鼠肝细胞中,实验结果表明,低渗性细胞肿胀后会出现RVD,而金鱼细胞肿胀时却没有伴随RVD(M.V. Espelt等人,2003年,《实验生物学杂志》206卷,513 - 522页)。模型预测数据与实验获得的数据之间的比较表明,在鳟鱼和大鼠肝细胞中,低渗性激活了一个传感元件,进而激活了原本沉默的KCl外流——其动力学能够被成功预测——从而导致容积下调。相比之下,关于金鱼肝细胞中不存在RVD的情况,所提出的模型表明,要么不存在触发RVD的传感元件,要么效应机制(KCl的丢失)在所采用的条件下仍处于非激活状态。与此一致的是,我们最近发现,细胞外核苷酸可能是诱导这些细胞中RVD所必需的,这表明我们的模型确实可以得出有用的预测。

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