| First Author | Xiong J | Year | 2018 |
| Journal | Mol Cell | Volume | 69 |
| Issue | 4 | Pages | 689-698.e7 |
| PubMed ID | 29429925 | Mgi Jnum | J:260808 |
| Mgi Id | MGI:6150120 | Doi | 10.1016/j.molcel.2018.01.010 |
| Citation | Xiong J, et al. (2018) A Metabolic Basis for Endothelial-to-Mesenchymal Transition. Mol Cell 69(4):689-698.e7 |
| abstractText | Endothelial-to-mesenchymal transition (EndoMT) is a cellular process often initiated by the transforming growth factor beta (TGF-beta) family of ligands. Although required for normal heart valve development, deregulated EndoMT is linked to a wide range of pathological conditions. Here, we demonstrate that endothelial fatty acid oxidation (FAO) is a critical in vitro and in vivo regulator of EndoMT. We further show that this FAO-dependent metabolic regulation of EndoMT occurs through alterations in intracellular acetyl-CoA levels. Disruption of FAO via conditional deletion of endothelial carnitine palmitoyltransferase II (Cpt2(E-KO)) augments the magnitude of embryonic EndoMT, resulting in thickening of cardiac valves. Consistent with the known pathological effects of EndoMT, adult Cpt2(E-KO) mice demonstrate increased permeability in multiple vascular beds. Taken together, these results demonstrate that endothelial FAO is required to maintain endothelial cell fate and that therapeutic manipulation of endothelial metabolism could provide the basis for treating a growing number of EndoMT-linked pathological conditions. |
