Posts Tagged ‘Dictyostelium’

Structured foraging of soil predators unveils functional responses to bacterial defenses

Fernando W. Rossine, Gabriel Vercelli, Corina Tarnita, and Thomas Gregor. Proceedings of the National Academy of Science (in press).


Eco-evolutionary significance of “loners”

Fernando W. Rossine, Ricardo Martinez-Garcia, Allyson E. Sgro, Thomas Gregor, Corina E. Tarnita. Eco-evolutionary significance of “loners”. PLoS Biol 18(3): e3000642 (2020). (more…)

Modeling oscillations and spiral waves in Dictyostelium populations

Javad Noorbakhsh, David J. Schwab, Allyson E. Sgro, Thomas Gregor, and Pankaj Mehta. Physical Review E 91: 062711 (2015).  (more…)

From Intracellular Signaling to Population Oscillations: Bridging Size and Time Scales in Collective Behavior

Allyson E. Sgro, David J. Schwab, Javad Noorbakhsh, Troy Mestler, Pankaj Mehta, and Thomas Gregor. Molecular Systems Biology 11: 799 (2015).  (more…)

1. Collective behaviors in living cell populations

One example of such new physics may lie in the emergence of collective behaviors in early developing cell populations and cell tissues. Cells are at the same time an ??active living agent?? while they are exposed to external chemical signaling and mechanical force fields. Combining these two properties, individuality and field dependence, is a fundamental issue across all the physical sciences that has not been resolved, neither theoretically nor experimentally. My laboratory approaches this question two fold: we study the emergence of multicellularity in starved cell populations of the social amoeba Dictyostelium, and we try to extract the mechanical tissue properties during the earliest stages of developing fly embryos.

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For the amoebae project, we have developed a novel optical sensor (based on Foerster-Resonance-Energy- Transfer technology), which allows for direct fluorescence measurements of intra-cellular signaling in develop- ing cell populations. We are currently designing cellular environments based on microfluidic technology to obtain a greater handle on the extracellular space (i.e. extracellular signaling molecule concentration measurements, generation of temporal and spatial concentration waves), allowing us to probe living cells at the single- and multi-cellular levels with great control. Further we are developing a phenomenological theoretical model in collaboration with Pankaj Mehta (Boston University/Physics) to bridge the gap between single cell properties and collective multicellular phenomena. In order to connect this top-down approach back to molecular detail of the cellular signaling cascade, we are measuring the single-cell signaling properties of various signaling mutants that display phenotypes at the macroscopic level. To this end, we are collaborating with Ted Cox in the Molecular Biology department in order to take advantage of his large mutagenesis database, which we combine with our optical sensors.

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The tissue mechanics project necessitates highly spatially and temporally resolved dynamic data of de- veloping fly embryos. My laboratory has set up microscopy to capture movies of living tissue in which individual nuclei are labeled optically. In collaboration with Andrea Liu (UPenn/Physics) and Lisa Manning (Syracuse/Physics) we are developing analysis tools to extract mechanical tissue properties from these movies. Preliminary re- sults generated by a novel cell tracking software suggest that mitotic divisions in Drosophila occur in a series of waves initiated in an excitable medium, i.e. one where waves are actively regenerated in the material. Our Dictyostelium work has also suggested that multicellular signaling proceeds by excitable, self-generated waves. The plan is to model both the mechanical and biochemical cell-cell (or nuclei-nuclei) interactions in these systems, to understand the mechanisms for wave propagation and tease apart the role of these excitable waves in multicellular organization.


The Onset of Collective Behavior in Social Amoebae

T. Gregor, K. Fujimoto, N. Masaki and S. Sawai, Science 328, 1021-1025 (2010).

Princeton’s father of the cellular slime mold

Here is a very nice feature on John Bonner, Princeton emeritus professor and Dictyostelium hero. With a standing activity of over 70 years of research, he is probably the longest living research contributor to the fascinating world of the social amoebae.

He discovered in 1947 that Dictyostelium cells are attracted by and chemotax towards a chemical called  cyclic adenosine monophosphate or cAMP. And it is only now, more than 60 years later that we can actually visualize and measure the concentration of this chemical in living Dictyostelium cells using an optical technology called FRET.

This is a sampler of Bonner’s outstanding movie collection that he started during his undergraduate days:

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If you want to read more on him please go here.

Abstracts from contributions to recent international Dictyostelium meeting in Tsukuba/Japan

Currently, I am in the process of finishing up my work on amoeba signaling and aggregation in Tokyo. This work is in collaboration with and in the laboratory of Satoshi Sawai at the University of Tokyo. We also collaborate with Koichi Fujimoto, a theorist at the same institution. While no papers have been published yet, as a preview pasted below are three abstracts of contributions to a recent international Dictyostelium meeting held in Tsukuba/Japan. (more…)

Classic papers on signaling and aggregation of amoebae

Over the next few months/years I’d like to use this website to build up a repository of information on the various topics that we study in the lab. Today as a beginning I am introducing 4 classic papers that pioneered a system-level description and quantitative understanding of this spectacular phenomenon:

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In this movie roughly 200 starved amoebae of the species Dictyostelium discoideum are shown over 8 hours during which they find each other and culminate in a cellular slime mould. This process is seen as a survival strategy because individual amoebae would die under starvation whereas as in the multi-cellular organism 80% of the cells can survive as spores. (more…)