| First Author | Wang L | Year | 2014 |
| Journal | J Biol Chem | Volume | 289 |
| Issue | 43 | Pages | 29827-35 |
| PubMed ID | 25202016 | Mgi Jnum | J:217760 |
| Mgi Id | MGI:5615541 | Doi | 10.1074/jbc.M114.597161 |
| Citation | Wang L, et al. (2014) Osmotic stress-induced phosphorylation of H2AX by polo-like kinase 3 affects cell cycle progression in human corneal epithelial cells. J Biol Chem 289(43):29827-35 |
| abstractText | Increased concentrations of extracellular solutes affect cell function and fate by stimulating cellular responses, such as evoking MAPK cascades, altering cell cycle progression, and causing apoptosis. Our study results here demonstrate that hyperosmotic stress induced H2AX phosphorylation (gammaH2AX) by an unrevealed kinase cascade involving polo-like kinase 3 (Plk3) in human corneal epithelial (HCE) cells. We found that hyperosmotic stress induced DNA-double strand breaks and increased gammaH2AX in HCE cells. Phosphorylation of H2AX at serine 139 was catalyzed by hyperosmotic stress-induced activation of Plk3. Plk3 directly interacted with H2AX and was colocalized with gammaH2AX in the nuclei of hyperosmotic stress-induced cells. Suppression of Plk3 activity by overexpression of a kinase-silencing mutant or by knocking down Plk3 mRNA effectively reduced gammaH2AX in hyperosmotic stress-induced cells. This was consistent with results that show gammaH2AX was markedly suppressed in the Plk3(-/-) knock-out mouse corneal epithelial layer in response to hyperosmotic stimulation. The effect of hyperosmotic stress-activated Plk3 and increased gammaH2AX in cell cycle progression showed an accumulation of G2/M phase, altered population in G1 and S phases, and increased apoptosis. Our results for the first time reveal that hyperosmotic stress-activated Plk3 elicited gammaH2AX. This Plk3-mediated activation of gammaH2AX subsequently regulates the cell cycle progression and cell fate. |
