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Echigoya, S.

Publications and source records attributed to Echigoya, S..

2 recordsLinked to original sources

Mechanical analysis of spatiotemporal traction stress dynamics in a bleb-driven migrating cell, Amoeba proteus

Many adherent eukaryotic cells exhibit amoeboid locomotion, where traction stress exerted on the substrate is essential for movement. In this study, we investigated the spatiotemporal development of these forces in Amoeba proteus to clarify the mechanical dynamics underlying bleb-driven migration. By performing a multipole analysis of the stress distribution, we characterized the spatiotemporal patterns exhibited by motile cells. Furthermore, we tracked the behavior of individual localized peak structures within these profiles, which are thought to correspond to focal contact sites. These analyses revealed that the front-back asymmetry in the traction distribution correlates with the direction of migration. We also found that A. proteus exhibits a periodic pattern in which inward-directed stresses are alternately strengthened and weakened at the cell poles. Crucially, we identified a distinctive feature not observed in other cell types: the generation of large lateral traction forces at the cell center. Together, these results highlight both the universality and diversity of the biophysical mechanisms driving amoeboid locomotion.

biophysics↗

Geometrical preference of anchoring sites in the unicellular organism Stentor coeruleus

Organisms often inhabit environments comprising complex structures across various scales. Animals rely on visual information from surrounding geometrical structures for navigation. Even at the microscale, various microsediments form complex structures in microbial habitats. The movement of microorganisms is passively affected by collisions and hydrodynamic interactions with surrounding structures. However, the influence of microenvironmental geometry on behavioral changes of unicellular organisms that lack visual perception remains unclear. Here, we developed geometrically structured chambers to investigate anchoring site preferences in the swimming ciliate Stentor coeruleus. Our experiments revealed that S. coeruleus preferentially anchored in narrow regions characterized by specific geometrical features, including corner angle, depth, and curvature at the corner end. Before anchoring, free-swimming S. coeruleus changed its behavior to move along the boundary wall of the chambers, accompanied by Ca2+-induced asymmetrical body deformation. To further investigate how S. coeruleus moves along the wall continuously, we conducted a hydrodynamic simulation and revealed that the asymmetric morphology causes asymmetric propulsive forces, explaining wall-following behavior through physical interactions with a wall. Thus, morphological change near a wall causes wall-following behavior, facilitating the identification of these narrow anchoring sites. Our findings indicate that environmental geometry drives behavioral transitions in S. coeruleus through simple biophysical processes, enabling spatial selection without visual cues. Overall, these results suggest that microgeometry plays a key role in shaping ecological niches for unicellular microorganisms. Significance StatementAnimals use various natural structures as landmarks for navigation. In microorganism habitats, microsediments also form geometrically complex environments. Is there a relationship between the geometrical features of structures and the behavior in unicellular organisms lacking visual cues? Here we report that the free-swimming unicellular organism Stentor coeruleus selects the anchoring sites based on the surrounding shapes. Further observations and numerical simulations reveal that an asymmetric morphological change causes a temporary switch from ballistic to wall-following exploration, driven by surrounding structures. These results indicate that one simple behavioral response underlies the preference of anchoring sites with specific geometrical features in non-neural unicellular organisms. The findings shed light on the role of microenvironmental geometry in forming ecological niches for microorganisms.

biophysics↗