| Literature DB >> 22819677 |
Denise Al Alam1, Frederic G Sala, Sheryl Baptista, Rosanna Galzote, Soula Danopoulos, Caterina Tiozzo, Philip Gage, Tracy Grikscheit, David Warburton, Mark R Frey, Saverio Bellusci.
Abstract
Fibroblast growth factor (FGF) signaling to the epithelium and mesenchyme mediated by FGF10 and FGF9, respectively, controls cecal formation during embryonic development. In particular, mesenchymal FGF10 signals to the epithelium via FGFR2b to induce epithelial cecal progenitor cell proliferation. Yet the precise upstream mechanisms controlling mesenchymal FGF10 signaling are unknown. Complete deletion of Fgf9 as well as of Pitx2, a gene encoding a homeobox transcription factor, both lead to cecal agenesis. Herein, we used mouse genetic approaches to determine the precise contribution of the epithelium and/or mesenchyme tissue compartments in this process. Using tissue compartment specific Fgf9 versus Pitx2 loss of function approaches in the gut epithelium and/or mesenchyme, we determined that FGF9 signals to the mesenchyme via Pitx2 to induce mesenchymal Fgf10 expression, which in turn leads to epithelial cecal bud formation.Entities:
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Year: 2012 PMID: 22819677 PMCID: PMC3725282 DOI: 10.1016/j.ydbio.2012.07.008
Source DB: PubMed Journal: Dev Biol ISSN: 0012-1606 Impact factor: 3.582