Echavarria-Heras Héctor, Leal-Ramirez Cecilia, Castillo Oscar
Modeling and Theoretical Analysis Research Group, Centro de Investigación Científica y de Educación Superior de Ensenada, Carretera Ensenada-Tijuana No, 3818, Zona Playitas, C, P, 22869 Ensenada, Baja California, México.
Theor Biol Med Model. 2014 May 22;11:23. doi: 10.1186/1742-4682-11-23.
Although the process of endocytosis of the low density lipoprotein (LDL) macromolecule and its receptor have been the subject of intense experimental research and modeling, there are still conflicting hypotheses and even conflicting data regarding the way receptors are transported to coated pits, the manner by which receptors are inserted before they aggregate in coated pits, and the display of receptors on the cell surface. At first it was considered that LDL receptors in human fibroblasts are inserted at random locations and then transported by diffusion toward coated pits. But experiments have not ruled out the possibility that the true rate of accumulation of LDL receptors in coated pits might be faster than predicted on the basis of pure diffusion and uniform reinsertion over the entire cell surface. It has been claimed that recycled LDL receptors are inserted preferentially in regions where coated pits form, with display occurring predominantly as groups of loosely associated units. Another mechanism that has been proposed by experimental cell biologists which might affect the accumulation of receptors in coated pits is a retrograde membrane flow. This is essentially linked to a polarized receptor insertion mode and also to the capping phenomenon, characterized by the formation of large patches of proteins that passively flow away from the regions of membrane exocytosis. In this contribution we calculate the mean travel time of LDL receptors to coated pits as determined by the ratio of flow strength to diffusion-coefficient, as well as by polarized-receptor insertion. We also project the resulting display of unbound receptors on the cell membrane. We found forms of polarized insertion that could potentially reduce the mean capture time of LDL receptors by coated pits which is controlled by diffusion and uniform insertion. Our results show that, in spite of its efficiency as a possible device for enhancement of the rate of receptor trapping, polarized insertion nevertheless fails to induce the formation of steady-state clusters of receptor on the cell membrane. Moreover, for appropriate values of the flow strength-diffusion ratio, the predicted steady-state distribution of receptors on the surface was found to be consistent with the phenomenon of capping.
尽管低密度脂蛋白(LDL)大分子及其受体的内吞过程一直是深入实验研究和建模的主题,但关于受体如何转运至被膜小窝、在聚集于被膜小窝之前如何插入以及在细胞表面的展示方式,仍存在相互矛盾的假说甚至相互矛盾的数据。起初,人们认为人成纤维细胞中的LDL受体随机插入,然后通过扩散向被膜小窝转运。但实验并未排除LDL受体在被膜小窝中真正的积累速率可能比基于纯扩散和在整个细胞表面均匀重新插入所预测的速率更快的可能性。有人声称,循环利用的LDL受体优先插入形成被膜小窝的区域,主要以松散关联的单元群形式展示。实验细胞生物学家提出的另一种可能影响受体在被膜小窝中积累的机制是逆向膜流。这本质上与极化受体插入模式以及封帽现象相关,封帽现象的特征是形成大量蛋白质斑块,这些斑块从膜胞吐区域被动地流走。在本论文中,我们计算了LDL受体到达被膜小窝的平均传播时间,该时间由流动强度与扩散系数的比值以及极化受体插入所决定。我们还预测了细胞膜上未结合受体的最终展示情况。我们发现了几种极化插入形式,它们有可能缩短LDL受体被被膜小窝捕获的平均时间,而该时间受扩散和均匀插入控制。我们的结果表明,尽管极化插入作为一种可能提高受体捕获速率的机制具有效率,但它仍然无法诱导细胞膜上形成受体的稳态簇。此外,对于流动强度 - 扩散比的适当值,发现表面受体的预测稳态分布与封帽现象一致。