Ramay Hena R, Vendelin Marko
Laboratory of Systems Biology, Institute of Cybernetics, Tallinn University of Technology, Tallinn, Estonia.
Biophys J. 2009 Jul 22;97(2):443-52. doi: 10.1016/j.bpj.2009.04.062.
Several experiments on permeabilized heart muscle fibers suggest the existence of diffusion restrictions grouping mitochondria and surrounding ATPases. The specific causes of these restrictions are not known, but intracellular structures are speculated to act as diffusion barriers. In this work, we assume that diffusion restrictions are induced by sarcoplasmic reticulum (SR), cytoskeleton proteins localized near SR, and crowding of cytosolic proteins. The aim of this work was to test whether such localization of diffusion restrictions would be consistent with the available experimental data and evaluate the extent of the restrictions. For that, a three-dimensional finite-element model was composed with the geometry based on mitochondrial and SR structural organization. Diffusion restrictions induced by SR and cytoskeleton proteins were varied with other model parameters to fit the set of experimental data obtained on permeabilized rat heart muscle fibers. There are many sets of model parameters that were able to reproduce all experiments considered in this work. However, in all the sets, <5-6% of the surface formed by SR and associated cytoskeleton proteins is permeable to metabolites. Such a low level of permeability indicates that the proteins should play a dominant part in formation of the diffusion restrictions.
多项针对透化心肌纤维的实验表明,存在将线粒体与周围的ATP酶聚集在一起的扩散限制。这些限制的具体原因尚不清楚,但据推测细胞内结构起到了扩散屏障的作用。在这项研究中,我们假设扩散限制是由肌浆网(SR)、位于SR附近的细胞骨架蛋白以及胞质蛋白的拥挤所诱导的。这项研究的目的是检验这种扩散限制的定位是否与现有的实验数据一致,并评估限制的程度。为此,构建了一个三维有限元模型,其几何形状基于线粒体和SR的结构组织。由SR和细胞骨架蛋白诱导的扩散限制随其他模型参数而变化,以拟合在透化大鼠心肌纤维上获得的一组实验数据。有许多组模型参数能够重现这项研究中考虑的所有实验。然而,在所有这些组中,由SR和相关细胞骨架蛋白形成的表面中,只有不到5 - 6%对代谢物具有通透性。如此低的通透性水平表明,这些蛋白质在扩散限制的形成中应起主要作用。