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Patients with the connective tissue disorder Loeys-Dietz syndrome (LDS) are at high risk for aortic aneurysm. LDS results in the presence of missense mutations within either of the genes encoding receptors for TGF-β. LDS-associated mutations are predicted to reduce TGF-β signaling; however, aortic tissue samples from LDS patients indicate that TGF-β signaling may be enhanced.
In this issue of the Journal of Clinical Investigation, Harry Dietz and colleagues at Johns Hopkins School of Medicine developed a mouse model of LDS, in which transgenic animals expressing Tgfbr1 or Tgfbr2 with LDS-associated mutations recapitulated human phenotypes. Using this model, the authors determined that even though the mutated TGF-β receptors were functionally defective, there was evidence of increased TGF-β signaling as indicated by elevated Smad2 phosphorylation. Furthermore, development of aortic aneurysms in these mice was ameliorated by treatment with an Angiotensin II type 1 (AT1) receptor antagonist.
In a companion commentary, Alan Daughtery and colleagues at the University of Kentucky discuss the therapeutic implications of this study on the use of AT1 receptor agonists to treat LDS-associated aneurism.
ACCOMPANYING COMMENTARY TITLE: Aortic aneurysms in Loeys-Dietz syndrome - a tale of two pathways?
Article adapted by Medical News Today from original press release. Click 'references' tab above for source.
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Journal of Clinical Investigation. "Dysfunctional TGF-beta signaling contributes to Loeys-Dietz syndrome-associated aortic aneurysm." Medical News Today. MediLexicon, Intl., 31 Dec. 2013. Web.
24 Apr. 2014. <http://www.medicalnewstoday.com/releases/270570>
Journal of Clinical Investigation. (2013, December 31). "Dysfunctional TGF-beta signaling contributes to Loeys-Dietz syndrome-associated aortic aneurysm." Medical News Today. Retrieved from
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