Liebovitch L S, Weinbaum S
Biophys J. 1981 Aug;35(2):315-38. doi: 10.1016/S0006-3495(81)84792-3.
To try to understand how an epithelial tissue can transport water between bathing solutions of equal tonicity and how intracellular solute and protein concentration are related to the structural specialization of the cell membrane at its apical, basal, and lateral margins, we have formulated and solved, using approximate analytical techniques, a new model which combines the detailed transport of local osmotic flow in extracellular channel with the multicompartment approach of thermodynamic models requiring the overall conservation of water and solute for the entire cell layer. Thus, unlike most previous models, which dealt exclusively with either the average properties of the cell layer or the local transport in the extracellular channel, we are able to solve simultaneously for the interaction of the cell with its environments across its apical, basal, and lateral cell membranes as well as the detailed transport in the extracellular channel. The model is then applied to corneal endothelium to obtain new insight into the water flow movement in this tissue under in vitro and in vivo conditions. Then in vitro solution shows that the cell at 297 mosmol/liter is slightly hypotonic to the 300-mosmol/liter external bathing solutions which drive water equally out both the aqueous (apical) and stromal (basal) cell faces. This water is replaced from the extracellular channel. There is a net flow of water because more water enters the channel through its open stromal end than through the higher resistance tight junction. In vivo, the solution predicts that the stromal swelling pressure forces water through the tight junctions towards the stroma so that there is no net flow. The interesting new features of our solution are the water recirculation pattern and the role of the osmotically active proteins in making the cell hypertonic relative to the channel.
为了试图理解上皮组织如何在等渗的浸浴溶液之间转运水,以及细胞内溶质和蛋白质浓度如何与细胞膜顶端、基底和侧面边缘的结构特化相关,我们使用近似分析技术构建并求解了一个新模型,该模型将细胞外通道中局部渗透流的详细转运与热力学模型的多隔室方法相结合,要求整个细胞层的水和溶质总体守恒。因此,与大多数先前仅处理细胞层平均特性或细胞外通道局部转运的模型不同,我们能够同时求解细胞通过其顶端、基底和侧面细胞膜与其环境的相互作用以及细胞外通道中的详细转运。然后将该模型应用于角膜内皮,以获得对该组织在体外和体内条件下水流动运动的新见解。体外溶液显示,297毫摩尔/升的细胞相对于300毫摩尔/升的外部浸浴溶液略呈低渗,后者将水均匀地从细胞的水相(顶端)和基质相(基底)表面排出。这些水由细胞外通道补充。存在水的净流动,因为通过其开放的基质端进入通道的水比通过更高阻力的紧密连接进入的水更多。在体内,该溶液预测基质肿胀压力迫使水通过紧密连接流向基质,从而不存在净流动。我们解决方案有趣的新特点是水的再循环模式以及渗透活性蛋白在使细胞相对于通道呈高渗方面的作用。