Cell migration orchestrates migrasome formation by shaping retraction fibers
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Updated: Oct 3, 2025

Measuring Cell-Edge Protrusion Dynamics during Spreading using Live-Cell Microscopy
Published on: November 1, 2021
Changyuan Fan1,2, Xuemeng Shi3,4, Kaikai Zhao5,6
1Unit of Cell Biology and Imaging Study of Pathogen Host Interaction, The Center for Microbes, Development and Health, CAS Key Laboratory of Molecular Virology and Immunology, Institut Pasteur of Shanghai, Chinese Academy of Sciences, Shanghai, China.
Abstract:
Migrasomes are recently discovered vesicle-like structures on retraction fibers of migrating cells that have been linked with transfer of cellular contents, shedding of unwanted materials, and information integration. However, whether and how the cell migration paradigm regulates migrasome formation is not clear. Here, we report that there are significantly fewer migrasomes in turning cells compared with straight persistently migrating cells. The major insight underlying this observation is that as the cells elongate, their rear ends become narrower, subsequently resulting in fewer retraction fibers during impersistent migration. In addition to migration persistence, we reveal that migration speed positively corelates with migrasome formation, owing to the derived length of retraction fibers. Substantiating our hypothesis, genetically removing vimentin compromises cell migration speed and persistence and leads to fewer migrasomes. Together, our data explicate the critical roles of two cell migration patterns, persistence and speed, in the control of migrasome formation by regulating retraction fibers.
Insights
Migrasome formation decreases in turning cells due to fewer retraction fibers. Cell migration speed and persistence, regulated by vimentin, are key factors controlling migrasome production.
Area of Science:
- Cell Biology
- Biophysics
- Cytoskeleton Dynamics
Background:
- Migrasomes are novel vesicle-like structures observed on cellular retraction fibers.
- Their formation and regulation, particularly concerning cell migration dynamics, remain poorly understood.
Purpose of the Study:
- To investigate the relationship between cell migration patterns (persistence and speed) and migrasome formation.
- To elucidate the underlying mechanisms by which cell migration regulates migrasome production.
Main Methods:
- Comparative analysis of migrasome numbers in straight versus turning migrating cells.
- Assessment of cell morphology, retraction fiber dynamics, and migration speed.
- Genetic manipulation involving vimentin to study its role in cell migration and migrasome formation.
Main Results:
- Turning cells exhibit significantly fewer migrasomes compared to persistently migrating cells.
- Reduced migrasome formation in turning cells is attributed to narrower rear ends and fewer retraction fibers.
- Cell migration speed positively correlates with migrasome formation, linked to retraction fiber length.
- Vimentin deficiency impairs cell migration speed and persistence, leading to decreased migrasome numbers.
Conclusions:
- Cell migration persistence and speed are critical regulators of migrasome formation.
- These migration parameters control migrasome production by influencing the dynamics and number of retraction fibers.
- The cytoskeleton, specifically vimentin, plays a crucial role in mediating the observed effects.
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