Fold-change detection and scale invariance of cell–cell signaling in social amoeba

Cell–cell signaling is subject to variability in the extracellular volume, cell number, and dilution that potentially increase uncertainty in the absolute concentrations of the extracellular signaling molecules. To direct cell aggregation, the social amoebae Dictyostelium discoideum collectively giv...

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Published inProceedings of the National Academy of Sciences - PNAS Vol. 114; no. 21; pp. E4149 - E4157
Main Authors Kamino, Keita, Kondo, Yohei, Nakajima, Akihiko, Honda-Kitahara, Mai, Kaneko, Kunihiko, Sawai, Satoshi
Format Journal Article
LanguageEnglish
Published United States National Academy of Sciences 23.05.2017
SeriesPNAS Plus
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Summary:Cell–cell signaling is subject to variability in the extracellular volume, cell number, and dilution that potentially increase uncertainty in the absolute concentrations of the extracellular signaling molecules. To direct cell aggregation, the social amoebae Dictyostelium discoideum collectively give rise to oscillations and waves of cyclic adenosine 3′,5′-monophosphate (cAMP) under a wide range of cell density. To date, the systems-level mechanism underlying the robustness is unclear. By using quantitative live-cell imaging, here we show that the magnitude of the cAMP relay response of individual cells is determined by fold change in the extracellular cAMP concentrations. The range of cell density and exogenous cAMP concentrations that support oscillations at the population level agrees well with conditions that support a large fold-change–dependent response at the single-cell level. Mathematical analysis suggests that invariance of the oscillations to density transformation is a natural outcome of combining secrete-and-sense systems with a fold-change detection mechanism.
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Edited by Peter N. Devreotes, The Johns Hopkins University School of Medicine, Baltimore, MD, and approved April 9, 2017 (received for review February 9, 2017)
Author contributions: K. Kamino, Y.K., K. Kaneko, and S.S. designed research; K. Kamino, Y.K., A.N., and S.S. performed research; M.H.-K. and S.S. contributed new reagents; K. Kamino and A.N. acquired and analyzed live cell image data; K. Kamino and Y.K. performed theoretical and computational analysis; and K. Kamino, Y.K., and S.S. wrote the paper.
ISSN:0027-8424
1091-6490
1091-6490
DOI:10.1073/pnas.1702181114