Circuit Design Features of a Stable Two-Cell System

Cell communication within tissues is mediated by multiple paracrine signals including growth factors, which control cell survival and proliferation. Cells and the growth factors they produce and receive constitute a circuit with specific properties that ensure homeostasis. Here, we used computationa...

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Veröffentlicht in:Cell 2018-02, Vol.172 (4), p.744-757.e17
Hauptverfasser: Zhou, Xu, Franklin, Ruth A., Adler, Miri, Jacox, Jeremy B., Bailis, Will, Shyer, Justin A., Flavell, Richard A., Mayo, Avi, Alon, Uri, Medzhitov, Ruslan
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Sprache:eng
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Zusammenfassung:Cell communication within tissues is mediated by multiple paracrine signals including growth factors, which control cell survival and proliferation. Cells and the growth factors they produce and receive constitute a circuit with specific properties that ensure homeostasis. Here, we used computational and experimental approaches to characterize the features of cell circuits based on growth factor exchange between macrophages and fibroblasts, two cell types found in most mammalian tissues. We found that the macrophage-fibroblast cell circuit is stable and robust to perturbations. Analytical screening of all possible two-cell circuit topologies revealed the circuit features sufficient for stability, including environmental constraint and negative-feedback regulation. Moreover, we found that cell-cell contact is essential for the stability of the macrophage-fibroblast circuit. These findings illustrate principles of cell circuit design and provide a quantitative perspective on cell interactions. [Display omitted] •Macrophages and fibroblasts form a stable cell circuit resilient to perturbations•Analytical screening reveals design principles for population stability•The MP and FB circuit maintains stability through a “spring-and-ceiling” model•Cell contact provides competitive advantage because of local exchange of growth factors How is the cellular composition of a tissue stably maintained?
ISSN:0092-8674
1097-4172
DOI:10.1016/j.cell.2018.01.015