Defective epithelial-mesenchymal interactions dictate the organogenesis oftracheoesophageal fistula

Citation
Ca. Crisera et al., Defective epithelial-mesenchymal interactions dictate the organogenesis oftracheoesophageal fistula, PEDIAT SURG, 16(4), 2000, pp. 256-261
Citations number
31
Categorie Soggetti
Pediatrics
Journal title
PEDIATRIC SURGERY INTERNATIONAL
ISSN journal
01790358 → ACNP
Volume
16
Issue
4
Year of publication
2000
Pages
256 - 261
Database
ISI
SICI code
0179-0358(200005)16:4<256:DEIDTO>2.0.ZU;2-W
Abstract
We have previously suggested that the fistula tract in esophageal atresia w ith tracheoesophageal fistula (EA/TEF) arises from a trifurcation of the em bryonic lung bud. Thus, it appears to be a respiratory-derived structure, a nd expresses the lung-specific transcription factor TTF-1 in its epithelium . The fistula tract does not give rise to lungs like the other branches fro m the bud. It grows caudally until it fistulizes with the stomach. We hypot hesized that epithelial-mesenchymal interactions (EMI) dictate the differen tial pattern of growth of the respiratory-derived fistula tract in EA/TEF. EA/TEF was induced in rat embryos via prenatal exposure to adriamycin. Micr odissection was performed on E13.5 embryos to isolate developing lung bud, fistula tract, or esophagus from adriamycin-treated or control animals, res pectively. The mesenchyme and epithelium from each of these foregut structu res were separated. The individual epithelia were recombined with each of t he various mesenchymes and grown in culture. They were assayed for relative degrees of branching. Isolated lung-bud epithelia (LBE) or fistula epithel ium were also cultured in Matrigel with exogenous fibroblast growth factors (FGF) and subsequently assayed for branching. The fistula-tract mesenchyme relatively inhibited branching of lung epithelium. The epithelium of the f istula tract could be induced to branch by non-fistula (lung or esophageal) mesenchyme. The fistula-tract and adriamycin-treated LEE both branched in response to FGF1. In contrast, neither responded to FGF7 or FGF10. EMI are defective in the developing EA/TEF. The inability to respond to FGF7 and FG F10 suggests an epithelial defect involving the receptor FGF2R-IIIb, to whi ch these mesenchymal factors obligately bind. Thus, the mesenchyme around t he developing fistula tract may lack an FGF branching morphogen(s), such as FGF1. Hence, this mesenchyme is unable to induce branching of respiratory epithelia and allows the middle branch of the embryonic tracheal trifurcati on to grow caudally as an unbranched tube until it fistulizes into the stom ach.