| First Author | Guimarães-Camboa N | Year | 2015 |
| Journal | Dev Cell | Volume | 33 |
| Issue | 5 | Pages | 507-21 |
| PubMed ID | 26028220 | Mgi Jnum | J:239361 |
| Mgi Id | MGI:5828368 | Doi | 10.1016/j.devcel.2015.04.021 |
| Citation | Guimaraes-Camboa N, et al. (2015) HIF1alpha Represses Cell Stress Pathways to Allow Proliferation of Hypoxic Fetal Cardiomyocytes. Dev Cell 33(5):507-21 |
| abstractText | Transcriptional mediators of cell stress pathways, including HIF1alpha, ATF4, and p53, are key to normal development and play critical roles in disease, including ischemia and cancer. Despite their importance, mechanisms by which pathways mediated by these transcription factors interact with one another are not fully understood. In addressing the controversial role of HIF1alpha in cardiomyocytes (CMs) during heart development, we discovered a mid-gestational requirement for HIF1alpha for proliferation of hypoxic CMs, involving metabolic switching and a complex interplay among HIF1alpha, ATF4, and p53. Loss of HIF1alpha resulted in activation of ATF4 and p53, the latter inhibiting CM proliferation. Bioinformatic and biochemical analyses revealed unexpected mechanisms by which HIF1alpha intersects with ATF4 and p53 pathways. Our results highlight previously undescribed roles of HIF1alpha and interactions among major cell stress pathways that could be targeted to enhance proliferation of CMs in ischemia and may have relevance to other diseases, including cancer. |
