TY - JOUR
T1 - Roundabout Receptors Are Critical for Foregut Separation from the Body Wall
AU - Domyan, Eric Thomas
AU - Branchfield, Kelsey
AU - Gibson, Daniel A.
AU - Naiche, L. A.
AU - Lewandoski, Mark
AU - Tessier-Lavigne, Marc
AU - Ma, Le
AU - Sun, Xin
PY - 2013/1/14
Y1 - 2013/1/14
N2 - In 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.
AB - In 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.
UR - http://www.scopus.com/inward/record.url?scp=84872385931&partnerID=8YFLogxK
U2 - 10.1016/j.devcel.2012.11.018
DO - 10.1016/j.devcel.2012.11.018
M3 - Article
C2 - 23328398
AN - SCOPUS:84872385931
SN - 1534-5807
VL - 24
SP - 52
EP - 63
JO - Developmental cell
JF - Developmental cell
IS - 1
ER -