Tzeghai G, Ganatos P, Pfeffer R, Weinbaum S, Nir A
J Theor Biol. 1986 Jul 21;121(2):141-62. doi: 10.1016/s0022-5193(86)80089-3.
A mathematical model is presented herein to determine the effect of convection on macromolecular transport across an artery wall due to transmural or osmotic pressure differences. The model is based on an extension of the leaky junction-cell turnover model of Weinbaum et al. (1985) to take into account a combined transport mechanism of convection and diffusion and also to provide the leaky junctions in the model with a finite resistance, thus allowing the results to be extended to intercellular clefts with a retarding extracellular matrix or to macromolecules whose dimensions are nearly the same as the junctional width. The results from this improved model show that the effect of pressure on transarterial macromolecular transport is important especially for cell turnover rates greater than 1% and that significant changes in the equilibrium balance of the cholesterol carrying LDL molecules in the arterial wall can occur due to a very small fraction of leaky junctions. At very high turnover rates (large fraction of leaky junctions) the effect of convection on macromolecular transport becomes dramatic and explains the very large increases in uptake observed experimentally after artificially inducing extensive endothelial damage.
本文提出了一个数学模型,以确定由于跨壁或渗透压差异导致的对流对大分子跨动脉壁转运的影响。该模型基于Weinbaum等人(1985年)的渗漏连接-细胞更新模型的扩展,以考虑对流和扩散的联合转运机制,并为模型中的渗漏连接提供有限阻力,从而使结果能够扩展到具有延迟细胞外基质的细胞间裂隙或尺寸与连接宽度几乎相同的大分子。这个改进模型的结果表明,压力对经动脉大分子转运的影响尤为重要,特别是对于细胞更新率大于1%的情况,并且由于非常小比例的渗漏连接,动脉壁中携带胆固醇的低密度脂蛋白分子的平衡会发生显著变化。在非常高的更新率(大量的渗漏连接)下,对流对大分子转运的影响变得显著,并解释了在人工诱导广泛内皮损伤后实验观察到的摄取量大幅增加的现象。