| First Author | Sawhney S | Year | 2015 |
| Journal | PLoS One | Volume | 10 |
| Issue | 2 | Pages | e0116270 |
| PubMed ID | 25643152 | Mgi Jnum | J:229054 |
| Mgi Id | MGI:5750278 | Doi | 10.1371/journal.pone.0116270 |
| Citation | Sawhney S, et al. (2015) Alpha-enolase is upregulated on the cell surface and responds to plasminogen activation in mice expressing a 133p53alpha mimic. PLoS One 10(2):e0116270 |
| abstractText | The p53 protein is a master regulator of the stress response. It acts as a tumor suppressor by inducing transcriptional activation of p53 target genes, with roles in apoptosis, cell cycle arrest and metabolism. The discovery of at least 12 isoforms of p53, some of which have tumor-promoting properties, has opened new avenues of research. Our previous work studied tumor phenotypes in four mouse models with different p53 backgrounds: wild-type p53, p53 null, mutant p53 lacking the proline domain (mDeltapro), and a mimic for the human Delta133p53alpha p53 isoform (Delta122p53). To identify the major proteins affected by p53 function early in the response to DNA damage, the current study investigated the entire proteome of bone marrow, thymus, and lung in the four p53 models. Protein extracts from untreated controls and those treated with amsacrine were analyzed using two-dimensional fluorescence difference gel electrophoresis. In the bone marrow, reactive proteins were universally decreased by wild-type p53, including alpha-enolase. Further analysis of alpha-enolase in the p53 models revealed that it was instead increased in Delta122p53 hematopoietic and tumor cell cytosol and on the cell surface. Alpha-enolase on the surface of Delta122p53 cells acted as a plasminogen receptor, with tumor necrosis factor alpha induced upon plasminogen stimulation. Taken together, these data identified new proteins associated with p53 function. One of these proteins, alpha-enolase, is regulated differently by wild-type p53 and Delta122p53 cells, with reduced abundance as part of a wild-type p53 response and increased abundance with Delta122p53 function. Increased cell surface alpha-enolase on Delta122p53 cells provides a possible explanation for the model's pro-inflammatory features and suggests that p53 isoforms may direct an inflammatory response by increasing the amount of alpha-enolase on the cell surface. |
