Keratin 19 maintains E-cadherin localization at the cell surface and stabilizes cell-cell adhesion of MCF7 cells.
Sarah AlsharifPooja SharmaKarina L BurschRachel MillikenVan LamArwa FallatahThuc PhanMeagan CollinsPriya DohlmanSarah TiufekchievGeorges NehmetallahChristopher B RaubByung Min ChungPublished in: Cell adhesion & migration (2022)
A cytoskeletal protein keratin 19 (K19) is highly expressed in breast cancer but its effects on breast cancer cell mechanics are unclear. In MCF7 cells where K19 expression is ablated,we found that K19 is required to maintain rounded epithelial-like shape and tight cell-cell adhesion. A loss of K19 also lowered cell surface E-cadherin levels. Inhibiting internalization restored cell-cell adhesion of KRT19 knockout cells, suggesting that E-cadherin internalization contributed to defective adhesion. Ultimately, while K19 inhibited cell migration and invasion, it was required for cells to form colonies in suspension. Our results suggest that K19 stabilizes E-cadherin complexes at the cell membrane to maintain cell-cell adhesion which inhibits cell invasiveness but provides growth and survival advantages for circulating tumor cells.
Keyphrases
- cell adhesion
- single cell
- induced apoptosis
- cell therapy
- cell surface
- cell cycle arrest
- circulating tumor cells
- stem cells
- signaling pathway
- oxidative stress
- blood brain barrier
- escherichia coli
- mesenchymal stem cells
- cell proliferation
- endoplasmic reticulum stress
- cystic fibrosis
- young adults
- breast cancer cells
- pi k akt
- amino acid
- cell migration