The effects of activin A on the migration of human breast cancer cells and neutrophils and their migratory interaction

Activin A belongs to the superfamily of transforming growth factor beta (TGFβ) and is a critical regulatory cytokine in breast cancer and inflammation. However, the role of activin A in migration of breast cancer cells and immune cells was not well characterized. Here, a microfluidic device was used...

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Veröffentlicht in:Experimental cell research 2017-08, Vol.357 (1), p.107-115
Hauptverfasser: Xie, Dongxue, Liu, Zhonghui, Wu, Jiandong, Feng, Wenfang, Yang, Ke, Deng, Jixian, Tian, Ganghong, Santos, Susy, Cui, Xueling, Lin, Francis
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Sprache:eng
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Zusammenfassung:Activin A belongs to the superfamily of transforming growth factor beta (TGFβ) and is a critical regulatory cytokine in breast cancer and inflammation. However, the role of activin A in migration of breast cancer cells and immune cells was not well characterized. Here, a microfluidic device was used to examine the effect of activin A on the migration of human breast cancer cell line MDA-MB-231 cells and human blood neutrophils as well as their migratory interaction. We found that activin A promoted the basal migration but impaired epidermal growth factor (EGF)-induced migration of breast cancer cells. By contrast, activin A reduced neutrophil chemotaxis and transendothelial migration to N-Formyl-Met-Leu-Phe (fMLP). Finally, activin A promoted neutrophil chemotaxis to the supernatant from breast cancer cell culture. Collectively, our study revealed the different roles of activin A in regulating the migration of breast cancer cells and neutrophils and their migratory interaction. These findings suggested the potential of activin A as a therapeutic target for inflammation and breast cancers. [Display omitted] •Activin A promotes breast cancer cell migration but impairs EGF-induced migration.•Activin A weakens neutrophil chemotaxis and transendothelial migration to fMLP.•Activin A potentiates migratory interaction between neutrophils and breast cancer.
ISSN:0014-4827
1090-2422
DOI:10.1016/j.yexcr.2017.05.003