Broad Institute of Massachusetts Institute of Technology and Harvard, Cambridge, MA, USA; Tananbaum Center for Theoretical and Analytical Human Biology, Yale University School of Medicine, New Haven, CT, USA.
School of Computer Science and Engineering, The Hebrew University of Jerusalem, Jerusalem, Israel.
Cell Rep. 2023 May 30;42(5):112412. doi: 10.1016/j.celrep.2023.112412. Epub 2023 Apr 21.
Most cell types in multicellular organisms can perform multiple functions. However, not all functions can be optimally performed simultaneously by the same cells. Functions incompatible at the level of individual cells can be performed at the cell population level, where cells divide labor and specialize in different functions. Division of labor can arise due to instruction by tissue environment or through self-organization. Here, we develop a computational framework to investigate the contribution of these mechanisms to division of labor within a cell-type population. By optimizing collective cellular task performance under trade-offs, we find that distinguishable expression patterns can emerge from cell-cell interactions versus instructive signals. We propose a method to construct ligand-receptor networks between specialist cells and use it to infer division-of-labor mechanisms from single-cell RNA sequencing (RNA-seq) and spatial transcriptomics data of stromal, epithelial, and immune cells. Our framework can be used to characterize the complexity of cell interactions within tissues.
多细胞生物中的大多数细胞类型都可以执行多种功能。然而,并非所有功能都能由同一细胞同时最佳地执行。在细胞群体水平上,可以执行在单个细胞水平上不兼容的功能,细胞在不同功能上分工合作,专门化。分工可以由组织环境的指令或通过自组织产生。在这里,我们开发了一个计算框架来研究这些机制对细胞群体内分工的贡献。通过在权衡条件下优化集体细胞任务性能,我们发现可区分的表达模式可以从细胞-细胞相互作用与指令信号中出现。我们提出了一种在专家细胞之间构建配体-受体网络的方法,并使用它从基质、上皮和免疫细胞的单细胞 RNA 测序(RNA-seq)和空间转录组学数据中推断分工机制。我们的框架可用于描述组织内细胞相互作用的复杂性。