| Literature DB >> 22772368 |
Mark E Lindsay1, Dorien Schepers, Nikhita Ajit Bolar, Jefferson J Doyle, Elena Gallo, Justyna Fert-Bober, Marlies J E Kempers, Elliot K Fishman, Yichun Chen, Loretha Myers, Djahita Bjeda, Gretchen Oswald, Abdallah F Elias, Howard P Levy, Britt-Marie Anderlid, Margaret H Yang, Ernie M H F Bongers, Janneke Timmermans, Alan C Braverman, Natalie Canham, Geert R Mortier, Han G Brunner, Peter H Byers, Jennifer Van Eyk, Lut Van Laer, Harry C Dietz, Bart L Loeys.
Abstract
Loeys-Dietz syndrome (LDS) associates with a tissue signature for high transforming growth factor (TGF)-β signaling but is often caused by heterozygous mutations in genes encoding positive effectors of TGF-β signaling, including either subunit of the TGF-β receptor or SMAD3, thereby engendering controversy regarding the mechanism of disease. Here, we report heterozygous mutations or deletions in the gene encoding the TGF-β2 ligand for a phenotype within the LDS spectrum and show upregulation of TGF-β signaling in aortic tissue from affected individuals. Furthermore, haploinsufficient Tgfb2(+/-) mice have aortic root aneurysm and biochemical evidence of increased canonical and noncanonical TGF-β signaling. Mice that harbor both a mutant Marfan syndrome (MFS) allele (Fbn1(C1039G/+)) and Tgfb2 haploinsufficiency show increased TGF-β signaling and phenotypic worsening in association with normalization of TGF-β2 expression and high expression of TGF-β1. Taken together, these data support the hypothesis that compensatory autocrine and/or paracrine events contribute to the pathogenesis of TGF-β-mediated vasculopathies.Entities:
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Year: 2012 PMID: 22772368 PMCID: PMC3616632 DOI: 10.1038/ng.2349
Source DB: PubMed Journal: Nat Genet ISSN: 1061-4036 Impact factor: 38.330