Pribyl Michal, Muratov Cyrill B, Shvartsman Stanislav Y
Department of Chemical Engineering and Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, New Jersey 08544, USA.
Biophys J. 2003 Jun;84(6):3624-35. doi: 10.1016/S0006-3495(03)75093-0.
Pattern formation in epithelial layers heavily relies on cell communication by secreted ligands. Whereas the experimentally observed signaling patterns can be visualized at single-cell resolution, a biophysical framework for their interpretation is currently lacking. To this end, we develop a family of discrete models of cell communication in epithelial layers. The models are based on the introduction of cell-to-cell coupling coefficients that characterize the spatial range of intercellular signaling by diffusing ligands. We derive the coupling coefficients as functions of geometric, cellular, and molecular parameters of the ligand transport problem. Using these coupling coefficients, we analyze a nonlinear model of positive feedback between ligand release and binding. In particular, we study criteria of existence of the patterns consisting of clusters of a few signaling cells, as well as the onset of signal propagation. We use our model to interpret recent experimental studies of the EGFR/Rhomboid/Spitz module in Drosophila development.
上皮层中的模式形成严重依赖于分泌配体介导的细胞通讯。虽然实验观察到的信号模式可以在单细胞分辨率下可视化,但目前缺乏用于解释这些模式的生物物理框架。为此,我们开发了一系列上皮层细胞通讯的离散模型。这些模型基于引入细胞间耦合系数,该系数表征了通过扩散配体进行细胞间信号传导的空间范围。我们将耦合系数推导为配体运输问题的几何、细胞和分子参数的函数。利用这些耦合系数,我们分析了配体释放与结合之间正反馈的非线性模型。特别地,我们研究了由少数信号细胞簇组成的模式的存在标准以及信号传播的起始。我们用我们的模型来解释果蝇发育中EGFR/类rhomboid蛋白酶/Spitz模块的近期实验研究。