| First Author | French SW | Year | 2012 |
| Journal | Exp Mol Pathol | Volume | 93 |
| Issue | 3 | Pages | 309-14 |
| PubMed ID | 22981937 | Mgi Jnum | J:316094 |
| Mgi Id | MGI:6832540 | Doi | 10.1016/j.yexmp.2012.09.002 |
| Citation | French SW, et al. (2012) FAT10 knock out mice livers fail to develop Mallory-Denk bodies in the DDC mouse model. Exp Mol Pathol 93(3):309-14 |
| abstractText | Mallory-Denk bodies (MDBs) are aggresomes composed of undigested ubiqutinated short lived proteins which have accumulated because of a decrease in the rate of their degradation by the 26s proteasome. The decrease in the activity of the proteasome is due to a shift in the activity of the 26s proteasome to the immunoproteasome triggered by an increase in expression of the catalytic subunits of the immunoproteasome which replaces the catalytic subunits of the 26s proteasome. This switch in the type of proteasome in liver cells is triggered by the binding of IFNgamma to the IFNgamma sequence response element (ISRE) located on the FAT10 promoter. To determine if either FAT10 or IFNgamma are essential for the formation of MDBs we fed both IFNgamma and FAT10 knock out (KO) mice DDC added to the control diet for 10weeks in order to induce MDBs. Mice fed the control diet and Wild type mice fed the DDC or control diet were compared. MDBs were located by immunofluorescent double stains using antibodies to ubiquitin to stain MDBs and FAT10 to localize the increased expression of FAT10 in MDB forming hepatocytes. We found that MDB formation occurred in the IFNgamma KO mice but not in the FAT10 KO mice. Western blots showed an increase in the ubiquitin smears and decreases beta 5 (chymotrypsin-like 26S proteasome subunit) in the Wild type mice fed DDC but not in the FAT10 KO mice fed DDC. To conclude, we have demonstrated that FAT10 is essential to the induction of MDB formation in the DDC fed mice. |
