Literature DB >> 22275045

Signaling by SHH rescues facial defects following blockade in the brain.

H Jonathan Chong1, Nathan M Young, Diane Hu, Juhee Jeong, Andrew P McMahon, Benedikt Hallgrimsson, Ralph S Marcucio.   

Abstract

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.

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Year:  2012        PMID: 22275045      PMCID: PMC3547623          DOI: 10.1002/dvdy.23726

Source DB:  PubMed          Journal:  Dev Dyn        ISSN: 1058-8388            Impact factor:   3.780


  36 in total

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5.  Hedgehog signaling in the neural crest cells regulates the patterning and growth of facial primordia.

Authors:  Juhee Jeong; Junhao Mao; Toyoaki Tenzen; Andreas H Kottmann; Andrew P McMahon
Journal:  Genes Dev       Date:  2004-04-15       Impact factor: 11.361

6.  Temporal perturbations in sonic hedgehog signaling elicit the spectrum of holoprosencephaly phenotypes.

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  28 in total

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2.  Neural crest cells utilize primary cilia to regulate ventral forebrain morphogenesis via Hedgehog-dependent regulation of oriented cell division.

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Journal:  Dev Biol       Date:  2017-09-21       Impact factor: 3.582

3.  Genetics of murine craniofacial morphology: diallel analysis of the eight founders of the Collaborative Cross.

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4.  Quantification of shape and cell polarity reveals a novel mechanism underlying malformations resulting from related FGF mutations during facial morphogenesis.

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6.  Correlations Between the Morphology of Sonic Hedgehog Expression Domains and Embryonic Craniofacial Shape.

Authors:  Qiuping Xu; Heather Jamniczky; Diane Hu; Rebecca M Green; Ralph S Marcucio; Benedikt Hallgrimsson; Washington Mio
Journal:  Evol Biol       Date:  2015-09       Impact factor: 3.119

7.  Maternal diet supplementation with methyl donors and increased parity affect the incidence of craniofacial defects in the offspring of twisted gastrulation mutant mice.

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Journal:  J Nutr       Date:  2013-01-23       Impact factor: 4.798

8.  Apaf1 apoptotic function critically limits Sonic hedgehog signaling during craniofacial development.

Authors:  A B Long; W J Kaiser; E S Mocarski; T Caspary
Journal:  Cell Death Differ       Date:  2013-07-26       Impact factor: 15.828

9.  miR-199 family contributes to regulation of sonic hedgehog expression during craniofacial development.

Authors:  Heather A Richbourg; Diane P Hu; Yanhua Xu; Andrea J Barczak; Ralph S Marcucio
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