Neutrophil extracellular traps activates focal adhesion kinase by upregulating MMP9 expression to promote proliferation and migration of mouse colorectal cancer cells.
- Author:
Yi HE
1
;
Songlin HOU
2
;
Changyuan MEMG
2
Author Information
1. The Second Department of Gastrointestinal Surgery, the Affiliated Hospital of North Sichuan Medical College, Nanchong 637000, China. *Corresponding author, E-mail: howardfine@163.com.
2. The Second Department of Gastrointestinal Surgery, the Affiliated Hospital of North Sichuan Medical College, Nanchong 637000, China.
- Publication Type:Journal Article
- MeSH:
Animals;
Mice;
Focal Adhesion Protein-Tyrosine Kinases/metabolism*;
Matrix Metalloproteinase 2/metabolism*;
Matrix Metalloproteinase 9/metabolism*;
Extracellular Traps/metabolism*;
Cell Movement;
Cell Proliferation;
RNA, Small Interfering/genetics*;
Colorectal Neoplasms/genetics*;
Cell Line, Tumor
- From:
Chinese Journal of Cellular and Molecular Immunology
2023;39(5):416-422
- CountryChina
- Language:Chinese
-
Abstract:
Objective To investigate how the neutrophil extracellular traps (NETs) affect the proliferation and migration of mouse MC38 colorectal cancer cells and its mechanism. Methods Spleen neutrophils were extracted in mouse, followed by collection of NETs after ionomycin stimulation in vitro. The proliferation of MC38 cell was detected by CCK-8 assay, and migration ability were detected by TranswellTM and cell scratch assay, after co-incubation with MC38 cells. The mRNA expression of cellular matrix metalloproteinase 2 (MMP2) and MMP9 were detected by real-time fluorescence quantitative PCR, and the expression of MMP2, MMP9 and focal adhesion kinase (FAK), phosphorylated FAK protein were detected by Western blot. After silencing MMP9 using small interfering RNA (siRNA), the effect of NETs on the proliferation and migration ability of MC38 cells and the altered expression of related molecules were examined by previous approach. Results NETs promoted the proliferation and migration of MC38 cells and up-regulated the MMP9 expression and FAK phosphorylation. Silencing MMP9 inhibited the promotion of MC38 proliferation and migration by NETs and suppressed FAK phosphorylation. Conclusion NETs up-regulates MMP9 expression in MC38 cells, activates FAK signaling pathway and promotes tumor cell proliferation and migration.
