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Three-dimensional balance of cortical tension and axial contractility enables fast amoeboid migration.


ABSTRACT: Fast amoeboid migration requires cells to apply mechanical forces on their surroundings via transient adhesions. However, the role these forces play in controlling cell migration speed remains largely unknown. We used three-dimensional force microscopy to measure the three-dimensional forces exerted by chemotaxing Dictyostelium cells, and examined wild-type cells as well as mutants with defects in contractility, internal F-actin crosslinking, and cortical integrity. We showed that cells pull on their substrate adhesions using two distinct, yet interconnected mechanisms: axial actomyosin contractility and cortical tension. We found that the migration speed increases when axial contractility overcomes cortical tension to produce the cell shape changes needed for locomotion. We demonstrated that the three-dimensional pulling forces generated by both mechanisms are internally balanced by an increase in cytoplasmic pressure that allows cells to push on their substrate without adhering to it, and which may be relevant for amoeboid migration in complex three-dimensional environments.

SUBMITTER: Alvarez-Gonzalez B 

PROVIDER: S-EPMC4336364 | biostudies-literature | 2015 Feb

REPOSITORIES: biostudies-literature

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Three-dimensional balance of cortical tension and axial contractility enables fast amoeboid migration.

Álvarez-González Begoña B   Meili Ruedi R   Bastounis Effie E   Firtel Richard A RA   Lasheras Juan C JC   Del Álamo Juan C JC  

Biophysical journal 20150201 4


Fast amoeboid migration requires cells to apply mechanical forces on their surroundings via transient adhesions. However, the role these forces play in controlling cell migration speed remains largely unknown. We used three-dimensional force microscopy to measure the three-dimensional forces exerted by chemotaxing Dictyostelium cells, and examined wild-type cells as well as mutants with defects in contractility, internal F-actin crosslinking, and cortical integrity. We showed that cells pull on  ...[more]

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