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ABSTRACT: Background
Sporadic aortic aneurysm and dissection (AAD), caused by progressive aortic smooth muscle cell (SMC) loss and extracellular matrix degradation, is a highly lethal condition. Identifying mechanisms that drive aortic degeneration is a crucial step in developing an effective pharmacologic treatment to prevent disease progression. Recent evidence has indicated that cytosolic DNA and abnormal activation of the cytosolic DNA sensing adaptor STING (stimulator of interferon genes) play a critical role in vascular inflammation and destruction. Here, we examined the involvement of this mechanism in aortic degeneration and sporadic AAD formation.Methods
The presence of cytosolic DNA in aortic cells and activation of the STING pathway were examined in aortic tissues from pat
SUBMITTER: Luo W
PROVIDER: S-EPMC6939474 | biostudies-literature | 2020 Jan
REPOSITORIES: biostudies-literature