Evidence map›Paper›PMID 41437214›Full record

ArticleBMC molecular and cell biology2025

Actomyosin dynamics in detached cells: linking clutch model to cell migration and cytokinesis.

Shigehiko Yumura, Yumi Kikuta, Go Itoh

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Article in BMC molecular and cell biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Shigehiko YumuraGraduate School of Sciences and Technology for Innovation, Yamaguchi University, Yamaguchi, 753-8512, Japan. yumura@yamaguchi-u.ac.jp.
Yumi KikutaGraduate School of Sciences and Technology for Innovation, Yamaguchi University, Yamaguchi, 753-8512, Japan.
Go ItohDepartment of Molecular Medicine and Biochemistry, Akita University Graduate School of Medicine, Akita, 010-8543, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCortical retrograde flow of actomyosin plays a critical role in cell migration and cytokinesis. While such flows have been extensively studied in adherent cells, their underlying mechanisms in non-adherent conditions remain poorly understood. In this study, we investigated actomyosin dynamics in Dictyostelium cells detached from the substratum, with a focus on cytoskeletal turnover and the applicability of the clutch hypothesis.

resultsDetached cells exhibited robust retrograde flows of actin and myosin II filaments within the cell cortex, moving at identical velocities. In contrast, membrane components and particles attached to the cell surface showed no movement, suggesting that the flows are driven by cortical actomyosin rather than membrane trafficking. Inhibition of actin polymerization completely abolished the flows, while myosin II inhibition had only a minor effect, indicating that actin polymerization is the primary driver. Flow velocities gradually decreased from the anterior to the posterior, consistent with a model in which actin filaments are pushed rearward rather than pulled from the back. Flow velocity was inversely proportional to cell migration speed, and nascent adhesion foci also moved retrogradely, supporting the clutch hypothesis, although Dictyostelium cells have neither canonical integrins nor well-defined extracellular matrix. Photobleaching experiments revealed that actin and myosin II filaments undergo turnover and recycling near the posterior. During cytokinesis under non-adherent conditions, cortical flows from the poles to the equator were significantly enhanced, and membrane components remained static. The clutch hypothesis may explain also the cortical flow and contractile ring formation during cytokinesis.

conclusionsOur findings demonstrate that detachment from the substratum induces dynamic, turnover-dependent actomyosin flows. These flows are primarily driven by actin polymerization and are consistent with the clutch hypothesis, which helps explain both cell migration and contractile ring formation during cytokinesis. This study expands the applicability of the clutch model and highlights the dynamic nature of the cytoskeleton in non-adherent cells.

Indexed as

ActomyosinCell MovementCytokinesisDictyosteliumActin CytoskeletonActinsCell AdhesionModels, BiologicalMyosin Type IIActinsActomyosinMyosin Type IIActinCell migrationCortical flowCytokinesisMyosinRetrograde flow

Identifiers

PMID41437214
PMCPMC12849310

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.