TWEAK promotes migration and invasion in MEFs through a mechanism dependent on ERKs activation and Fibulin 3 down‐regulation
| Autor: | Almudena Porras, Celia Sequera, Ana Vázquez-Carballo, María Arechederra, Sonia Fernández-Veledo |
|---|---|
| Rok vydání: | 2017 |
| Předmět: |
0301 basic medicine
Time Factors Physiology p38 mitogen-activated protein kinases Clinical Biochemistry Down-Regulation Extracellular matrix Mice 03 medical and health sciences Mitogen-Activated Protein Kinase 11 Downregulation and upregulation Cell Movement Animals Extracellular Signal-Regulated MAP Kinases Protein kinase B Cells Cultured Cytokine TWEAK Extracellular Matrix Proteins Chemistry Cell Biology Fibroblasts Fibulin Cell biology Enzyme Activation 030104 developmental biology Cancer cell Signal transduction Proto-Oncogene Proteins c-akt Signal Transduction |
| Zdroj: | Journal of Cellular Physiology. 233:968-978 |
| ISSN: | 1097-4652 0021-9541 |
| Popis: | TWEAK regulates multiple physio-pathological processes in fibroblasts such as fibrosis. It also induces migration and invasion in tumors and it can activate p38 MAPK in various cell types. Moreover, p38α MAPK promotes migration and invasion in several cancer cells types and in mouse embryonic fibroblasts (MEFs). However, it remains unknown if TWEAK could promote migration in fibroblasts and whether p38α MAPK might play a role. Our results reveal that TWEAK activates ERKs, Akt, and p38α/β MAPKs and reduces secreted Fibulin 3 in MEFs. TWEAK also increases migration and invasion in wt and p38α deficient MEFs, which indicates that p38α MAPK is not required to mediate these effects. In contrast, ERKs inhibition significantly decreases TWEAK-induced migration and Fibulin 3 knock-down mimics TWEAK effect. These results indicate that both ERKs activation and Fibulin 3 down-regulation would contribute to mediate TWEAK pro-migratory effect. In fact, the additional regulation of ERKs and/or p38β as a consequence of Fibulin 3 decrease might be also involved in the pro-migratory effect of TWEAK in MEFs. In conclusion, our studies uncover novel mechanisms by which TWEAK would favor tissue repair by promoting fibroblasts migration. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
|
Plný text