Membrane Flow Drives an Adhesion-Independent Amoeboid Cell Migration Mode.

Authors:
Xenia Meshik
Xenia Meshik
Washington University School of Medicine
United States
Vani Kalyanaraman
Vani Kalyanaraman
Washington University School of Medicine
United States
Krystal Melgarejo
Krystal Melgarejo
Washington University School of Medicine
St. Louis | United States

Dev Cell 2018 07 21;46(1):9-22.e4. Epub 2018 Jun 21.

Department of Anesthesiology, Washington University School of Medicine, St. Louis, MO 63110, USA; Department of Genetics, Washington University School of Medicine, St. Louis, MO 63110, USA. Electronic address:

Cells migrate by applying rearward forces against extracellular media. It is unclear how this is achieved in amoeboid migration, which lacks adhesions typical of lamellipodia-driven mesenchymal migration. To address this question, we developed optogenetically controlled models of lamellipodia-driven and amoeboid migration. On a two-dimensional surface, migration speeds in both modes were similar. However, when suspended in liquid, only amoeboid cells exhibited rapid migration accompanied by rearward membrane flow. These cells exhibited increased endocytosis at the back and membrane trafficking from back to front. Genetic or pharmacological perturbation of this polarized trafficking inhibited migration. The ratio of cell migration and membrane flow speeds matched the predicted value from a model where viscous forces tangential to the cell-liquid interface propel the cell forward. Since this mechanism does not require specific molecular interactions with the surrounding medium, it can facilitate amoeboid migration observed in diverse microenvironments during immune function and cancer metastasis.

Abstract Video

How cells in liquid suspension migrate


Source: Cell Press

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Source
http://dx.doi.org/10.1016/j.devcel.2018.05.029DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6048972PMC

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July 2018
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