Extracellular Hydraulic Resistance Enhances Cell Migration. Issue 29 (28th August 2022)

• Record Type: Journal Article
• Authors: Maity, Debonil; Bera, Kaustav; Li, Yizeng; Ge, Zhuoxu; Ni, Qin; Konstantopoulos, Konstantinos; Sun, Sean X.
• Is Part Of: Advanced science. Volume 9:Issue 29(2022)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2022-08-28
• Subjects: cancer -- cell migration -- osmotic engine model -- tumor microenvironment -- viscosity; Science -- Periodicals; 505
• DOI: 10.1002/advs.202200927
• Languages: English
• ISSNs: 2198-3844

Abstract

Abstract: Cells migrating in vivo encounter microenvironments with varying physical properties. One such physical variable is the fluid viscosity surrounding the cell. Increased viscosity is expected to increase the hydraulic resistance experienced by the cell and decrease cell speed. The authors demonstrate that contrary to this expected result, cells migrate faster in high viscosity media on 2‐dimensional substrates. Both actin dynamics and water dynamics driven by ion channel activity are examined. Results show that cells increase in area in high viscosity and actomyosin dynamics remain similar. Inhibiting ion channel fluxes in high viscosity media results in a large reduction in cell speed, suggesting that water flux contributes to the observed speed increase. Moreover, inhibiting actin‐dependent vesicular trafficking that transports ion channels to the cell boundary changes ion channel spatial positioning and reduces cell speed in high viscosity media. Cells also display altered Ca 2+ activity in high viscosity media, and when cytoplasmic Ca 2+ is sequestered, cell speed reduction and altered ion channel positioning are observed. Taken together, it is found that the cytoplasmic actin‐phase and water‐phase are coupled to drive cell migration in high viscosity media, in agreement with physical modeling that also predicts the observed cell speedup in high viscosity environments. Abstract : The speed of a moving object in a fluid should decrease with increasing fluid viscosity. It is found that this is not true for moving mammalian cells, which speed up in high viscosity media. It is discovered that cells can sense the media viscosity. Ion channels and active water flux contribute to this observed cell speedup.