| First Author | Lindhurst MJ | Year | 2020 |
| Journal | Hum Mol Genet | Volume | 29 |
| Issue | 20 | Pages | 3350-3360 |
| PubMed ID | 33030203 | Mgi Jnum | J:298839 |
| Mgi Id | MGI:6488350 | Doi | 10.1093/hmg/ddaa216 |
| Citation | Lindhurst MJ, et al. (2020) Ubiquitous expression of Akt1 p.(E17K) results in vascular defects and embryonic lethality in mice. Hum Mol Genet 29(20):3350-3360 |
| abstractText | Proteus syndrome is a progressive overgrowth disorder with vascular malformations caused by mosaic expression of the AKT1 c.49G > A, p.(E17K) activating variant which was predicted to cause lethality if expressed ubiquitously. To test that hypothesis, we used the ACTB-Cre gene to activate a conditional Akt1 p.(E17K) allele in the mouse. No offspring that was heterozygous for both Cre and the conditional allele (betaA-Akt1WT/flx) was viable. Fewer than expected numbers of betaA-Akt1WT/flx embryos were seen beginning at E11.5, but a few survived until E17.5. The phenotype ranged from mild to severe, but generally betaA-Akt1WT/flx embryos had fewer visible blood vessels and more hemorrhages than their wild-type littermates, which was suggestive of a vascular abnormality. Examination of E13.5 limb skin showed a primitive capillary network with increased branching complexity and abnormal patterning compared with wild-type skin. By E15.5, wild-type skin had undergone angiogenesis and formed a hierarchical network of remodeled vessels, whereas in betaA-Akt1WT/flx embryos, the capillary network failed to remodel. Mural cell coverage of the blood vessels was also reduced in betaA-Akt1WT/flx skin compared with that of wild type. Restricting expression of Akt1E17K to endothelial, cardiac or smooth muscle cells resulted in viable offspring and remodeled vasculature and did not recapitulate the betaA-Akt1WT/flx phenotype. We conclude that ubiquitous expression of Akt1E17K suppresses remodeling and inhibits the formation of a normal skin vasculature. We postulate that this failure prevents proper circulation necessary to support the growing embryo and that it is the result of interactions of multiple cell types with increased AKT signaling. |
