| Literature DB >> 19581825 |
Caterina Tiozzo1, Stijn De Langhe, Gianni Carraro, Denise Al Alam, Andre Nagy, Clarence Wigfall, Mohammad K Hajihosseini, David Warburton, Parviz Minoo, Saverio Bellusci.
Abstract
Patients with Apert syndrome (AS) display a wide range of congenital malformations including tracheal stenosis, which is a disease characterized by a uniform cartilaginous sleeve in place of a normally ribbed cartilagenous trachea. We have studied the cellular and molecular basis of this phenotype in a mouse model of AS (Fgfr2c(+/Delta) mice), which shows ectopic expression of Fgfr2b in mesenchymal tissues. Here we report that tracheal stenosis is associated with increased proliferation of mesenchymal cells, where the expression of Fgf10 and its upstream regulators Tbx4 and Tbx5 are abnormally elevated. We show that Fgf10 has a critical inductive role in tracheal stenosis, as genetic knockdown of Fgf10 in Fgfr2c(+/Delta) mice rescues this phenotype. These novel findings demonstrate a regulatory role for Fgf10 in tracheal development and shed more light on the underlying cause of tracheal defects in AS.Entities:
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Year: 2009 PMID: 19581825 PMCID: PMC3725279 DOI: 10.1203/PDR.0b013e3181b45580
Source DB: PubMed Journal: Pediatr Res ISSN: 0031-3998 Impact factor: 3.756