| First Author | Li X | Year | 2017 |
| Journal | Int J Mol Sci | Volume | 18 |
| Issue | 7 | PubMed ID | 28703745 |
| Mgi Jnum | J:277017 | Mgi Id | MGI:6296331 |
| Doi | 10.3390/ijms18071518 | Citation | Li X, et al. (2017) The Construction and Characterization of Mitochondrial Ferritin Overexpressing Mice. Int J Mol Sci 18(7):1518 |
| abstractText | Mitochondrial ferritin (FtMt) is a H-ferritin-like protein which localizes to mitochondria. Previous studies have shown that this protein can protect mitochondria from iron-induced oxidative damage, while FtMt overexpression in cultured cells decreases cytosolic iron availability and protects against oxidative damage. To investigate the in vivo role of FtMt, we established FtMt overexpressing mice by pro-nucleus microinjection and examined the characteristics of the animals. We first confirmed that the protein levels of FtMt in the transgenic mice were increased compared to wild-type mice. Interestingly, we found no significant differences in the body weights or organ to body weight ratios between wild type and transgenic mice. To determine the effects of FtMt overexpression on baseline murine iron metabolism and hematological indices, we measured serum, heart, liver, spleen, kidney, testis, and brain iron concentrations, liver hepcidin expression and red blood cell parameters. There were no significant differences between wild type and transgenic mice. In conclusion, our results suggest that FtMt overexpressing mice have no significant defects and the overexpression of FtMt does not affect the regulation of iron metabolism significantly in transgenic mice. |
