Programming self-organizing multicellular structures with synthetic cell-cell signaling

被引:321
|
作者
Toda, Satoshi [1 ,2 ]
Blauch, Lucas R. [3 ]
Tang, Sindy K. Y. [3 ]
Morsut, Leonardo [1 ,2 ,4 ]
Lim, Wendell A. [1 ,2 ]
机构
[1] Univ Calif San Francisco, Howard Hughes Med Inst, Dept Cellular & Mol Pharmacol, San Francisco, CA 94158 USA
[2] Univ Calif San Francisco, Ctr Syst & Synthet Biol, San Francisco, CA 94158 USA
[3] Stanford Univ, Dept Mech Engn, Stanford, CA 94305 USA
[4] Univ Southern Calif, Eli & Edythe Broad CIRM Ctr Regenerat Med & Stem, Los Angeles, CA 90033 USA
基金
日本学术振兴会;
关键词
POSITIONAL INFORMATION; DEVELOPMENTAL BIOLOGY; PATTERN-FORMATION; SPECIFICATION; CADHERINS; DETERMINANTS; UNDERSTAND; BEHAVIORS; ADHESION; COMPLEX;
D O I
10.1126/science.aat0271
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
收藏
页码:156 / +
页数:7
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