Department of Cellular and Molecular Pharmacology, Howard Hughes Medical Institute, and Center for Systems and Synthetic Biology, University of California, San Francisco, CA 94158, USA.
Department of Mechanical Engineering, Stanford University, Stanford, CA 94305, USA.
Science. 2018 Jul 13;361(6398):156-162. doi: 10.1126/science.aat0271. Epub 2018 May 31.
A common theme in the self-organization of multicellular tissues is the use of cell-cell signaling networks to induce morphological changes. We used the modular synNotch juxtacrine signaling platform to engineer artificial genetic programs in which specific cell-cell contacts induced changes in cadherin cell adhesion. Despite their simplicity, these minimal intercellular programs were sufficient to yield assemblies with hallmarks of natural developmental systems: robust self-organization into multidomain structures, well-choreographed sequential assembly, cell type divergence, symmetry breaking, and the capacity for regeneration upon injury. The ability of these networks to drive complex structure formation illustrates the power of interlinking cell signaling with cell sorting: Signal-induced spatial reorganization alters the local signals received by each cell, resulting in iterative cycles of cell fate branching. These results provide insights into the evolution of multicellularity and demonstrate the potential to engineer customized self-organizing tissues or materials.
细胞间信号网络诱导形态变化是多细胞组织自组织的一个常见主题。我们使用模块化的 synNotch 旁分泌信号平台来设计人工遗传程序,其中特定的细胞-细胞接触诱导钙黏蛋白细胞黏附的变化。尽管这些程序非常简单,但这些最小的细胞间程序足以产生具有自然发育系统特征的组装体:强大的自组织成多域结构、精心编排的顺序组装、细胞类型分化、对称性破坏以及在受伤后再生的能力。这些网络驱动复杂结构形成的能力说明了将细胞信号与细胞分选相连接的强大功能:信号诱导的空间重组改变了每个细胞接收到的局部信号,从而导致细胞命运分支的迭代循环。这些结果为多细胞生物的进化提供了新的见解,并展示了设计定制自组织组织或材料的潜力。