Deletion of Chromosome 9p21 Noncoding Cardiovascular Risk Interval in Mice Alters Smad2 Signaling and Promotes Vascular Aneurysm

作者：Loinard Celine; Basatemur Gemma; Masters Leanne; Baker Lauren; Harrison James; Figg Nichola; Vilar Jose; Sage Andrew P; Mallat Ziad^*

来源：Circulation-Cardiovascular Genetics, 2014, 7(6): 799-805.

DOI：10.1161/CIRCGENETICS.114.000696

• aneurysm
• genetics
• models, animal
• myocytes, smooth muscle

Background-Vascular aneurysm is an abnormal local dilatation of an artery that can lead to vessel rupture and sudden death. The only treatment involves surgical or endovascular repair or exclusion. There is currently no approved medical therapy for this condition. Recent data established a strong association between genetic variants in the 9p21 chromosomal region in humans and the presence of cardiovascular diseases, including aneurysms. However, the mechanisms linking this 9p21 DNA variant to cardiovascular risk are still unknown. %26lt;br%26gt;Methods and Results-Here, we show that deletion of the orthologous 70-kb noncoding interval on mouse chromosome 4 (chr4(Delta 70kb/Delta 70kb) mice) is associated with reduced aortic expression of cyclin-dependent kinase inhibitor genes p19Arf and p15Inkb. Vascular smooth muscle cells from chr4(Delta 70kb/Delta 70kb) mice show reduced transforming growth factor-beta-dependent canonical Smad2 signaling but increased cyclin-dependent kinase-dependent Smad2 phosphorylation at linker sites, a phenotype previously associated with tumor growth and consistent with the mechanistic link between reduced canonical transforming growth factor-beta signaling and susceptibility to vascular diseases. We also show that targeted deletion of the 9p21 risk interval promotes susceptibility to aneurysm development and rupture when mice are subjected to a validated model of aneurysm formation. The vascular disease of chr4(Delta 70kb/Delta 70kb) mice is prevented by treatment with a cyclin-dependent kinase inhibitor. %26lt;br%26gt;Conclusions-The results establish a direct mechanistic link between 9p21 noncoding risk interval and susceptibility to aneurysm and may have important implications for the understanding and treatment of vascular diseases.

• 出版日期2014-12