Literature DB >> 9603428

Fate map of the developing chick face: analysis of expansion of facial primordia and establishment of the primary palate.

I M McGonnell1, J D Clarke, C Tickle.   

Abstract

Developing facial primordia change shape substantially in stages leading up to primary palate formation. We investigated expansion of cell populations within each of the four facial primordia of chick embryos between HH-stages 20 and 28, by using DiI labelling. Populations of cells centred around the nasal pits in the upper face, the midline of the paired mandibular primordia in the lower face, and at sites of fusion contribute most to overall expansion. Abundant Msx-1 transcripts are found in regions of high expansion, and Fgf-8 transcripts are seen in ectoderm associated with some of these regions. Many cell populations display preferential expansion along one axis. Maxillary and mandibular primordia cell populations expand along the proximodistal axis, whereas at the distal tip of the frontonasal mass, cell populations expand mediolaterally. Thus outgrowth occurs at the tips of mandibular and maxillary primordia, but at the base of the frontonasal mass. At regions where adjacent primordia abut each other, we found bidirectional movement of cells between primordia, unidirectional movement or could detect no movement at all. Regions of highest expansion in each primordium have the highest percentage of S phase labelled cells. Cell death occurs in some regions of low expansion but it seems likely that cell rearrangements and intercalations also contribute to shaping. These rearrangements could be associated with stretching of the primordia by neighbouring tissues. Treatment of chick embryos with retinoic acid causes clefts of the primary palate (Tamarin et al. [1984] J. Embryol. Exp. Morphol. 84:105-123). We found a decrease in expansion of cell populations that normally contribute to primary palate formation but surprisingly little ectopic cell death. Expansion of other cell populations in the treated upper face was more even rather than directed. This further supports the idea that tension exerted by neighbouring tissues plays a major role in global shaping of the upper face.

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Year:  1998        PMID: 9603428     DOI: 10.1002/(SICI)1097-0177(199805)212:1<102::AID-AJA10>3.0.CO;2-9

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


  13 in total

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Review 3.  Recent insights into the morphological diversity in the amniote primary and secondary palates.

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Journal:  Dev Dyn       Date:  2015-09-10       Impact factor: 3.780

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5.  Prx1 and Prx2 cooperatively regulate the morphogenesis of the medial region of the mandibular process.

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Journal:  Dev Dyn       Date:  2009-10       Impact factor: 3.780

6.  Twisted gastrulation limits apoptosis in the distal region of the mandibular arch in mice.

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Journal:  Dev Biol       Date:  2009-01-20       Impact factor: 3.582

7.  Avian facial morphogenesis is regulated by c-Jun N-terminal kinase/planar cell polarity (JNK/PCP) wingless-related (WNT) signaling.

Authors:  Poongodi Geetha-Loganathan; Suresh Nimmagadda; Katherine Fu; Joy M Richman
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8.  Evolution of a developmental mechanism: Species-specific regulation of the cell cycle and the timing of events during craniofacial osteogenesis.

Authors:  Jane Hall; Andrew H Jheon; Erin L Ealba; B Frank Eames; Kristin D Butcher; Siu-Shan Mak; Raj Ladher; Tamara Alliston; Richard A Schneider
Journal:  Dev Biol       Date:  2013-11-18       Impact factor: 3.582

Review 9.  Beyond cell proliferation in avian facial morphogenesis.

Authors:  Marta Linde-Medina; Benedikt Hallgrímsson; Ralph Marcucio
Journal:  Dev Dyn       Date:  2016-01-04       Impact factor: 3.780

Review 10.  Palatal and oral manifestations of Muenke syndrome (FGFR3-related craniosynostosis).

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Journal:  J Craniofac Surg       Date:  2012-05       Impact factor: 1.046

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