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Annexins II and V inhibit cell migration
1Department of Cellular and Molecular Physiology, University of Cincinnati College of Medicine, Ohio 45236-0576, USA.
Experimental Cell Research
|January 22, 1998
Summary
Extracellular annexins II and V inhibit the migration of highly metastatic Lewis lung carcinoma cells. Antibodies against annexin II enhanced cell migration, suggesting annexins regulate cell movement.
Area of Science:
- Cell Biology
- Biochemistry
- Oncology
Background:
- Cell motility is essential for wound healing, development, and tumor metastasis.
- Extracellular annexins are calcium- and phospholipid-binding proteins with potential roles in cellular processes.
- Lewis lung carcinoma cells are highly metastatic, making them a relevant model for studying cancer cell migration.
Purpose of the Study:
- To investigate the role of extracellular annexins in the migration of Lewis lung carcinoma cells.
- To determine if specific annexins (II and V) affect cancer cell motility.
- To explore the mechanism by which annexins might influence cell migration.
Main Methods:
- Utilized wound closure assays to assess cell migration in vitro.
- Employed transwell migration assays with 8-micron pores to quantify cell movement.
- Administered anti-annexin II antibodies and control antibodies (anti-calmodulin) to evaluate their effects on cell migration.
Main Results:
- Annexins II and V significantly inhibited the migration of Lewis lung carcinoma cells by over 40%.
- Treatment with anti-annexin II antibodies led to enhanced cell migration in the wound closure assay.
- Control anti-calmodulin antibodies did not affect cell migration, indicating specificity of annexin effects.
Conclusions:
- Extracellular annexins II and V play an inhibitory role in the migration of highly metastatic Lewis lung carcinoma cells.
- Annexin II's inhibitory effect on cell migration may be reversed by specific antibodies, suggesting a regulatory function.
- The mechanism likely involves annexin-membrane interactions and interference with phospholipid dynamics crucial for membrane protrusion during migration.