| Literature DB >> 23636094 |
Yoshito Yamashiro1, Christina L Papke1, Yuichi Ikeda2,3, Jianbin Huang1, Yanling Lin1, Miteshkumar Patel1, Tadashi Inagami4, Victoria P Le5, Jessica E Wagenseil5, Hiromi Yanagisawa1.
Abstract
Aortic aneurysms are life-threatening and often associated with defects in connective tissues and mutations in smooth muscle cell (SMC) contractile proteins. Despite recent advances in understanding altered signaling in aneurysms of Marfan syndrome, the underlying mechanisms and options for pharmacological treatment for other forms of aneurysms are still under investigation. We previously showed in mice that deficiency in the fibulin-4 gene in vascular SMCs (Fbln4(SMKO)) leads to loss of the SMC contractile phenotype, hyperproliferation, and ascending aortic aneurysms. We report that abnormal up-regulation of angiotensin-converting enzyme (ACE) in SMCs and subsequent activation of angiotensin II (AngII) signaling are involved in the onset of aortic aneurysms in Fbln4(SMKO) mice. In this model, aneurysm formation was completely prevented by inhibition of the AngII pathway with losartan or captopril within a narrow therapeutic window during the first month of life, even though the altered mechanical properties of blood vessel walls were not reversed by the pharmacological treatment. The therapeutic effects of losartan in Fbln4(SMKO) mice do not require the AngII receptor type 2 (Agtr2) but likely require both type 1a (Agtr1a) and 1b (Agtr1b) receptors. The results indicate that fibulin-4 is a vascular matrix component required for regulation of local angiotensin signaling and development and maintenance of the SMC phenotype.Entities:
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Year: 2013 PMID: 23636094 PMCID: PMC3867808 DOI: 10.1126/scitranslmed.3005025
Source DB: PubMed Journal: Sci Transl Med ISSN: 1946-6234 Impact factor: 17.956