Cell migration orchestrates migrasome formation by shaping retraction fibers

Author:

Fan Changyuan12,Shi Xuemeng34ORCID,Zhao Kaikai56,Wang Linbo7,Shi Kun34ORCID,Liu Yan-Jun8ORCID,Li Hui7,Ji Baohua56ORCID,Jiu Yaming1234ORCID

Affiliation:

1. Unit 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

2. University of Chinese Academy of Sciences, Beijing, China

3. The Joint Program in Infection and Immunity, Guangzhou Women and Children’s Medical Center, Guangzhou Medical University, Guangzhou, China

4. The Joint Program in Infection and Immunity, Institut Pasteur of Shanghai, Chinese Academy of Sciences, Shanghai, China

5. Wenzhou Institute, University of Chinese Academy of Sciences, Wenzhou, China

6. Biomechanics and Mechanomedicine Laboratory, Department of Engineering Mechanics, Zhejiang University, Hangzhou, China

7. Suzhou Institute of Biomedical Engineering and Technology, Chinese Academy of Sciences, Suzhou, Jiangsu, China

8. Shanghai Institute of Cardiovascular Diseases, Shanghai Key Laboratory of Medical Epigenetics, International Co-laboratory of Medical Epigenetics and Metabolism (Ministry of Science and Technology), Institutes of Biomedical Sciences, Department of Systems Biology for Medicine, Zhongshan Hospital, Fudan University, 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.

Funder

National Natural Science Foundation of China

CAS-VPST Silk Road Science

Ministry of Science and Technology of China

Shanghai Municipal Science and Technology

Institut Pasteur of Shanghai

Publisher

Rockefeller University Press

Subject

Cell Biology

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