Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Programmed cell death and cell transformation in craniofacial development

C F Shuler1

  • 1University of Southern California, School of Dentistry, Center for Craniofacial Molecular Biology, Los Angeles 90033, USA.

Critical Reviews in Oral Biology and Medicine : an Official Publication of the American Association of Oral Biologists
|January 1, 1995
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Smad2 overexpression reduces the proliferation of the junctional epithelium.

Journal of dental research·2014
Same author

Evaluation of student and faculty perceptions of the PBL curriculum at two dental schools from a student perspective: a cross-sectional survey.

European journal of dental education : official journal of the Association for Dental Education in Europe·2007
Same author

Effects of diet consistency on the expression of insulin-like growth factors (IGFs), IGF receptors and IGF binding proteins during the development of rat masseter muscle soon after weaning.

Archives of oral biology·2004
Same author

Keeping the curriculum current with research and problem-based learning.

The Journal of the American College of Dentists·2002
Same author

Inherited risks for susceptibility to dental caries.

Journal of dental education·2001
Same author

Antagonistic effects of Smad2 versus Smad7 are sensitive to their expression level during tooth development.

The Journal of biological chemistry·2001
Same journal

Oral health, atherosclerosis, and cardiovascular disease.

Critical reviews in oral biology and medicine : an official publication of the American Association of Oral Biologists·2004
Same journal

The use of enamel matrix derivative in the treatment of periodontal defects: a literature review and meta-analysis.

Critical reviews in oral biology and medicine : an official publication of the American Association of Oral Biologists·2004
Same journal

Pathogenesis of apical periodontitis and the causes of endodontic failures.

Critical reviews in oral biology and medicine : an official publication of the American Association of Oral Biologists·2004
Same journal

The role of TGF-beta in epithelial malignancy and its relevance to the pathogenesis of oral cancer (part II).

Critical reviews in oral biology and medicine : an official publication of the American Association of Oral Biologists·2004
Same journal

TGF-beta signal transduction in oro-facial health and non-malignant disease (part I).

Critical reviews in oral biology and medicine : an official publication of the American Association of Oral Biologists·2004
Same journal

It is time to move on.....

Critical reviews in oral biology and medicine : an official publication of the American Association of Oral Biologists·2004
See all related articles

Craniofacial development involves branchial arch fusion, where ectodermal epithelia initially adhere but must be removed. Programmed cell death, epithelial-mesenchymal transformation, or migration are key mechanisms for this removal during palate fusion.

Area of Science:

  • Developmental biology
  • Craniofacial development
  • Epithelial biology

Background:

  • Branchial arch fusion is critical for forming craniofacial structures like the mandible, lips, and palate.
  • Ectodermal epithelia play a role in initial tissue adherence during fusion.
  • The medial edge epithelium of palatal shelves must be removed for successful palate fusion.

Purpose of the Study:

  • To review the mechanisms responsible for epithelial cell removal from fusion zones during craniofacial development.
  • To discuss programmed cell death, epithelial-mesenchymal transformation, and epithelial migration as potential removal mechanisms.
  • To examine these mechanisms in the context of palatal fusion and other model systems.

Main Methods:

  • Literature review of developmental biology studies.

Related Experiment Videos

  • Analysis of morphologic and molecular events in branchial arch fusion.
  • Comparison of findings across different model systems for epithelial cell removal.
  • Main Results:

    • Epithelial cells initially mediate adherence between fusing branchial arch processes.
    • These cells are absent from the final fusion zone, necessitating their removal.
    • Programmed cell death, epithelial-mesenchymal transformation, and migration are hypothesized fates for these cells.

    Conclusions:

    • The disappearance of medial edge epithelium is essential for secondary palate fusion.
    • Multiple cellular mechanisms likely contribute to epithelial removal during craniofacial development.
    • Understanding these processes is key to comprehending craniofacial morphogenesis.