Abstract

Chemotaxis is a ubiquitous biological phenomenon in which cells detect a spatial gradient of chemoattractant, and then move towards the source. Here we present a position-dependent advection-diffusion model that quantitatively describes the statistical features of the chemotactic motion of the social amoeba Dictyostelium discoideum in a linear gradient of cAMP (cyclic adenosine monophosphate). We fit the model to experimental trajectories that are recorded in a microfluidic setup with stationary cAMP gradients and extract the diffusion and drift coefficients in the gradient direction. Our analysis shows that for the majority of gradients, both coefficients decrease over time and become negative as the cells crawl up the gradient. The extracted model parameters also show that besides the expected drift in the direction of the chemoattractant gradient, we observe a nonlinear dependency of the corresponding variance on time, which can be explained by the model. Furthermore, the results of the model show that the non-linear term in the mean squared displacement of the cell trajectories can dominate the linear term on large time scales.

Highlights

  • Dictyostelium discoideum (D.d.) is a well-established model organism for cellular motility

  • We have analyzed large data sets of D.d. chemotaxis in linear gradients of cAMP recorded by Theves et al in a microfluidic setup.[7,8,13]

  • Data sets with different steepnesses of the cAMP gradient were included in our analysis, covering a large range of gradients, in which chemotactic behavior was observed

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Summary

Introduction

Dictyostelium discoideum (D.d.) is a well-established model organism for cellular motility. Chemotactic competent D.d. cells are highly motile and exhibit fast amoeboid movements with a velocity of 10–20 mm minÀ1 on glass substrates.[1,2,3] The chemotactic cell motion is highly organized over a length scale significantly larger than the size of a single cell (B10 mm). Cells sense gradients of cAMP and direct their chemotactic movements towards regions of higher concentration of cAMP.[4] When chemotactic attraction prevails over diffusion, the chemotaxis can trigger a self-accelerating process until aggregation takes place. 105–106 cells stream towards the aggregation centers and eventually transform into millimeter long slugs and form fruiting bodies bearing spores for long-term survival and long-range dispersal.[5]

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