The Ordered Extension of Pseudopodia by Amoeboid Cells in the Absence of External Cues

Eukaryotic cells extend pseudopodia for movement. In the absence of external cues, cells move in random directions, but with a strong element of persistence that keeps them moving in the same direction Persistence allows cells to disperse over larger areas and is instrumental to enter new environments where spatial cues can lead the cell. Here we explore cell movement by analyzing the direction, size and timing of ∼2000 pseudopodia that are extended by Dictyostelium cells. The results show that pseudpopod are extended perpendicular to the surface curvature at the place where they emerge. The location of new pseudopods is not random but highly ordered. Two types of pseudopodia may be formed: frequent splitting of an existing pseudopod, or the occasional extension of a de novo pseudopod at regions devoid of recent pseudopod activity. Split-pseudopodia are extended at ∼60 degrees relative to the previous pseudopod, mostly as alternating Right/Left/Right steps leading to relatively straight zigzag runs. De novo pseudopodia are extended in nearly random directions thereby interrupting the zigzag runs. Persistence of cell movement is based on the ratio of split versus de novo pseudopodia. We identify PLA2 and cGMP signaling pathways that modulate this ratio of splitting and de novo pseudopodia, and thereby regulate the dispersal of cells. The observed ordered extension of pseudopodia in the absence of external cues provides a fundamental insight into the coordinated movement of cells, and might form the basis for movement that is directed by internal or external cues.

[1]  P. Devreotes,et al.  Distinct roles of PI(3,4,5)P3 during chemoattractant signaling in Dictyostelium: a quantitative in vivo analysis by inhibition of PI3-kinase. , 2006, Molecular biology of the cell.

[2]  C. Patlak Random walk with persistence and external bias , 1953 .

[3]  Thomas D Pollard,et al.  Regulation of actin filament assembly by Arp2/3 complex and formins. , 2007, Annual review of biophysics and biomolecular structure.

[4]  R L Hall,et al.  Amoeboid movement as a correlated walk , 1977, Journal of mathematical biology.

[5]  M. Carlier,et al.  Regulation of actin assembly associated with protrusion and adhesion in cell migration. , 2008, Physiological reviews.

[6]  M J Potel,et al.  Preaggregative cell motion in Dictyostelium. , 1979, Journal of cell science.

[7]  Hiroaki Takagi,et al.  Functional Analysis of Spontaneous Cell Movement under Different Physiological Conditions , 2008, PloS one.

[8]  Till Bretschneider,et al.  Analysis of cell movement by simultaneous quantification of local membrane displacement and fluorescent intensities using Quimp2. , 2009, Cell motility and the cytoskeleton.

[9]  Miki Y. Matsuo,et al.  Ordered Patterns of Cell Shape and Orientational Correlation during Spontaneous Cell Migration , 2008, PloS one.

[10]  D. Soll,et al.  A novel cGMP signalling pathway mediating myosin phosphorylation and chemotaxis in Dictyostelium , 2002, EMBO Journal.

[11]  P. Devreotes,et al.  Chemotaxis: signalling the way forward , 2004, Nature Reviews Molecular Cell Biology.

[12]  John G. Collard,et al.  The Par-Tiam1 Complex Controls Persistent Migration by Stabilizing Microtubule-Dependent Front-Rear Polarity , 2007, Current Biology.

[13]  P. Iglesias,et al.  PIP3-Independent Activation of TorC2 and PKB at the Cell's Leading Edge Mediates Chemotaxis , 2008, Current Biology.

[14]  J. Xu,et al.  Neutrophil microtubules suppress polarity and enhance directional migration. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[15]  D. Taylor,et al.  Local and spatially coordinated movements in Dictyostelium discoideum amoebae during chemotaxis , 1982, Cell.

[16]  M H Gail,et al.  The locomotion of mouse fibroblasts in tissue culture. , 1970, Biophysical journal.

[17]  Liang Li,et al.  Persistent Cell Motion in the Absence of External Signals: A Search Strategy for Eukaryotic Cells , 2008, PloS one.

[18]  Edward A. Codling,et al.  Random walk models in biology , 2008, Journal of The Royal Society Interface.

[19]  P. V. van Haastert,et al.  Four key signaling pathways mediating chemotaxis in Dictyostelium discoideum , 2008, The Journal of cell biology.

[20]  P. V. van Haastert,et al.  Quimp3, an automated pseudopod-tracking algorithm , 2010, Cell adhesion & migration.

[21]  D. Dormann,et al.  Simultaneous quantification of cell motility and protein-membrane-association using active contours. , 2002, Cell motility and the cytoskeleton.

[22]  Pablo A Iglesias,et al.  tsunami, the Dictyostelium homolog of the Fused kinase, is required for polarization and chemotaxis. , 2008, Genes & development.

[23]  R. Insall,et al.  PIR121 Regulates Pseudopod Dynamics and SCAR Activity in Dictyostelium , 2003, Current Biology.

[24]  R. Kay,et al.  Changing directions in the study of chemotaxis , 2008, Nature Reviews Molecular Cell Biology.

[25]  T. Pollard The cytoskeleton, cellular motility and the reductionist agenda , 2003, Nature.

[26]  R. Firtel,et al.  Signaling pathways controlling cell polarity and chemotaxis. , 2001, Trends in biochemical sciences.

[27]  P. V. van Haastert,et al.  Guanylyl cyclase protein and cGMP product independently control front and back of chemotaxing Dictyostelium cells. , 2006, Molecular biology of the cell.

[28]  P. V. van Haastert,et al.  Essential role of PI3-kinase and phospholipase A2 in Dictyostelium discoideum chemotaxis , 2007, The Journal of cell biology.

[29]  P. Iglesias,et al.  PLA2 and PI3K/PTEN pathways act in parallel to mediate chemotaxis. , 2007, Developmental cell.

[30]  Christopher Janetopoulos,et al.  Directional sensing during chemotaxis , 2008, FEBS letters.

[31]  Natalie Andrew,et al.  Chemotaxis in shallow gradients is mediated independently of PtdIns 3-kinase by biased choices between random protrusions , 2007, Nature Cell Biology.

[32]  P. Devreotes,et al.  Two phases of actin polymerization display different dependencies on PI(3,4,5)P3 accumulation and have unique roles during chemotaxis. , 2003, Molecular biology of the cell.