Primary enamel knot cell death in Apaf-1 and caspase-9 deficient mice
Language English Country Great Britain, England Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
Grant support
Wellcome Trust - United Kingdom
PubMed
17055447
DOI
10.1016/j.archoralbio.2006.07.006
PII: S0003-9969(06)00212-3
Knihovny.cz E-resources
- MeSH
- Apoptosis physiology MeSH
- Cell Division physiology MeSH
- Epithelial Cells cytology MeSH
- Apoptotic Protease-Activating Factor 1 deficiency MeSH
- Caspase 9 deficiency MeSH
- Mesoderm physiology MeSH
- Molar embryology physiology MeSH
- Mice, Knockout MeSH
- Mice MeSH
- Proliferating Cell Nuclear Antigen analysis MeSH
- Dental Enamel embryology physiology MeSH
- Tooth Germ anatomy & histology embryology MeSH
- Animals MeSH
- Check Tag
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Apaf1 protein, mouse MeSH Browser
- Apoptotic Protease-Activating Factor 1 MeSH
- Caspase 9 MeSH
- Proliferating Cell Nuclear Antigen MeSH
During molar development, apoptosis occurs in a well-characterised pattern suggesting several roles for cell death in odontogenesis. However, molecular mechanisms of dental apoptosis are only poorly understood. In this study, Apaf-1 and caspase-9 knockouts were used to uncover the engagement of these members of the apoptotic machinery during early tooth development, concentrating primarily on their function in the apoptotic elimination of primary enamel knot cells. Molar tooth germ morphology, proliferation and apoptosis were investigated on frontal histological sections of murine heads at embryonic days (ED) 15.5, the stage when the primary enamel knot is eliminated apoptotically. In molar tooth germs of both knockouts, no apoptosis was observed according to morphological (haematoxylin-eosin) as well as biochemical criteria (TUNEL). Morphology of the mutant tooth germs, however, was not changed. Additionally, knockout mice showed no changes in proliferation compared to wild type mice. According to our findings on knockout embryos, Apaf-1 and caspase-9 are involved in apoptosis during tooth development; however, they seem dispensable and not necessary for proper tooth shaping. Compensatory or other mechanisms of cell death may act to eliminate the primary enamel knot cells in the absence of Apaf-1 and caspase-9.
References provided by Crossref.org
Exploring caspase functions in mouse models
Making the head: Caspases in life and death
Role of Cell Death in Cellular Processes During Odontogenesis
Apoptotic signaling in mouse odontogenesis