TY - JOUR
T1 - Signaling by SHH rescues facial defects following blockade in the brain
AU - Chong, H. Jonathan
AU - Young, Nathan M.
AU - Hu, Diane
AU - Jeong, Juhee
AU - McMahon, Andrew P.
AU - Hallgrimsson, Benedikt
AU - Marcucio, Ralph S.
PY - 2012/2
Y1 - 2012/2
N2 - Background: The Frontonasal Ectodermal Zone (FEZ) is a signaling center in the face that expresses Sonic hedgehog (Shh) and regulates patterned growth of the upper jaw. Blocking SHH in the forebrain blocks Shh expression in the FEZ and creates malformations resembling holoprosencephaly (HPE), while inhibition of BMP signaling in the mesenchyme blocks FEZ formation and causes similar dysmorphology. Thus, the brain could regulate FEZ formation by SHH or BMP signaling, and if so, activating one of these pathways in the face might alleviate the effects of repression of SHH in the brain. Results: We blocked SHH signaling in the brain while adding SHH or BMP between the neural and facial ectoderm of the frontonasal process. When applied early, SHH restored Shh expression in the FEZ and significantly improved shape outcomes, which contrasts with our previous experiments that showed later SHH treatments have no effect. BMP-soaked beads introduced early and late caused apoptosis that exacerbated malformations. Finally, removal of Smoothened from neural crest cells did not inhibit Shh expression in the FEZ. Conclusions: Collectively, this work suggests that a direct, time-sensitive SHH signal from the brain is required for the later induction of Shh in the FEZ. We propose a testable model of FEZ activation and discuss signaling mediators that may regulate these interactions.
AB - Background: The Frontonasal Ectodermal Zone (FEZ) is a signaling center in the face that expresses Sonic hedgehog (Shh) and regulates patterned growth of the upper jaw. Blocking SHH in the forebrain blocks Shh expression in the FEZ and creates malformations resembling holoprosencephaly (HPE), while inhibition of BMP signaling in the mesenchyme blocks FEZ formation and causes similar dysmorphology. Thus, the brain could regulate FEZ formation by SHH or BMP signaling, and if so, activating one of these pathways in the face might alleviate the effects of repression of SHH in the brain. Results: We blocked SHH signaling in the brain while adding SHH or BMP between the neural and facial ectoderm of the frontonasal process. When applied early, SHH restored Shh expression in the FEZ and significantly improved shape outcomes, which contrasts with our previous experiments that showed later SHH treatments have no effect. BMP-soaked beads introduced early and late caused apoptosis that exacerbated malformations. Finally, removal of Smoothened from neural crest cells did not inhibit Shh expression in the FEZ. Conclusions: Collectively, this work suggests that a direct, time-sensitive SHH signal from the brain is required for the later induction of Shh in the FEZ. We propose a testable model of FEZ activation and discuss signaling mediators that may regulate these interactions.
KW - Bone morphogenetic proteins (Bmp)
KW - Craniofacial development
KW - FFrontonasal process (FNP)
KW - Frontonasal ectodermal zone (FEZ)
KW - Holoprosencephaly (HPE)
KW - Sonic hedgehog (Shh)
UR - http://www.scopus.com/inward/record.url?scp=84856203355&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84856203355&partnerID=8YFLogxK
U2 - 10.1002/dvdy.23726
DO - 10.1002/dvdy.23726
M3 - Article
C2 - 22275045
AN - SCOPUS:84856203355
SN - 1058-8388
VL - 241
SP - 247
EP - 256
JO - Developmental Dynamics
JF - Developmental Dynamics
IS - 2
ER -