کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
2176898 | 1094596 | 2013 | 12 صفحه PDF | دانلود رایگان |
SummaryIn mammals, precise placement of organs is essential for survival. We show here that inactivation of Roundabout (Robo) receptors 1 and 2 in mice leads to mispositioning of the stomach in the thoracic instead of the abdominal cavity, which likely contributes to poor lung inflation and lethality at birth, reminiscent of congenital diaphragmatic hernia (CDH) cases in humans. Unexpectedly, in Robo mutant mice, the primary defect preceding organ misplacement and diaphragm malformation is a delayed separation of foregut from the dorsal body wall. Foregut separation is a rarely considered morphogenetic event, and our data indicate that it occurs via repulsion of Robo-expressing foregut cells away from the Slit ligand source. In humans, genomic lesions containing Robo genes have been documented in CDH. Our findings suggest that separation of the foregut from the body wall is genetically controlled and that defects in this event may contribute to CDH.
► Robo1;2 mutants show defects reminiscent of congenital diaphragmatic hernia (CDH)
► The primary defect in Robo mutants is delayed foregut separation from the body wall
► Loss of Robo impedes repulsion of foregut cells away from Slit source
► The foregut-separation defect precedes and may contribute to CDH-like pathologies
Journal: - Volume 24, Issue 1, 14 January 2013, Pages 52–63