Age-related changes in the tooth-bone interface area of acrodont dentition in the chameleon
Language English Country England, Great Britain Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
27173578
PubMed Central
PMC4974546
DOI
10.1111/joa.12490
Knihovny.cz E-resources
- Keywords
- acrodont dentition, laser-induced breakdown spectroscopy, micro-computed tomography, reptiles,
- MeSH
- Jaw anatomy & histology MeSH
- Dentition * MeSH
- Lizards MeSH
- Tooth Calcification physiology MeSH
- X-Ray Microtomography MeSH
- Aging MeSH
- Tooth anatomy & histology physiology MeSH
- Animals MeSH
- Check Tag
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
Chameleon teeth develop as individual structures at a distance from the developing jaw bone during the pre-hatching period and also partially during the post-hatching period. However, in the adult, all teeth are fused together and tightly attached to the jaw bone by mineralized attachment tissue to form one functional unit. Tooth to bone as well as tooth to tooth attachments are so firm that if injury to the oral cavity occurs, several neighbouring teeth and pieces of jaw can be broken off. We analysed age-related changes in chameleon acrodont dentition, where ankylosis represents a physiological condition, whereas in mammals, ankylosis only occurs in a pathological context. The changes in hard-tissue morphology and mineral composition leading to this fusion were analysed. For this purpose, the lower jaws of chameleons were investigated using X-ray micro-computed tomography, laser-induced breakdown spectroscopy and microprobe analysis. For a long time, the dental pulp cavity remained connected with neighbouring teeth and also to the underlying bone marrow cavity. Then, a progressive filling of the dental pulp cavity by a mineralized matrix occurred, and a complex network of non-mineralized channels remained. The size of these unmineralized channels progressively decreased until they completely disappeared, and the dental pulp cavity was filled by a mineralized matrix over time. Moreover, the distribution of calcium, phosphorus and magnesium showed distinct patterns in the different regions of the tooth-bone interface, with a significant progression of mineralization in dentin as well as in the supporting bone. In conclusion, tooth-bone fusion in chameleons results from an enhanced production of mineralized tissue during post-hatching development. Uncovering the developmental processes underlying these outcomes and performing comparative studies is necessary to better understand physiological ankylosis; for that purpose, the chameleon can serve as a useful model species.
CEITEC Central European Institute of Technology Brno University of Technology Brno Czech Republic
Department of Chemistry Faculty of Science Masaryk University Brno Czech Republic
Department of Experimental Biology Masaryk University Brno Czech Republic
Department of Oral and Maxillofacial Surgery University Hospital Ostrava Ostrava Czech Republic
Faculté de Chirurgie Dentaire Université de Strasbourg Strasbourg France
See more in PubMed
Abdel‐Salam ZA, Galmed AH, Tognoni E, et al. (2007) Estimation of calcified tissues hardness via calcium and magnesium ionic to atomic line intensity ratio in laser induced breakdown spectra. Spectrochim Acta, Part B 62, 1343–1347.
Akiba N, Sasano Y, Suzuki O, et al. (2006) Characterization of dentin formed in transplanted rat molars by electron probe microanalysis. Calcif Tissue Int 78, 143–151. PubMed
Alfaqeeh SA, Gaete M, Tucker AS (2013) Interactions of the tooth and bone during development. J Dent Res 92, 1129–1135. PubMed
Althoff J, Quint P, Krefting ER, et al. (1982) Morphological studies on the epiphyseal growth plate combined with biochemical and X‐ray microprobe analyses. Histochemistry 74, 541–552. PubMed
Anderson CV, Deban SM (2010) Ballistic tongue projection in chameleons maintains high performance at low temperature. Proc Natl Acad Sci U S A 107, 5495–5499. PubMed PMC
Andersson L, Malmgren B (1999) The problem of dentoalveolar ankylosis and subsequent replacement resorption in the growing patient. Aust Endod J 25, 57–61. PubMed
Aoba T, Moreno EC, Shimoda S (1992a) Competitive adsorption of magnesium and calcium ions onto synthetic and biological apatites. Calcif Tissue Int 51, 143–150. PubMed
Aoba T, Shimoda S, Moreno EC (1992b) Labile or surface pools of magnesium, sodium, and potassium in developing porcine enamel mineral. J Dent Res 71, 1826–1831. PubMed
Arnold WH, Gaengler P (2007) Quantitative analysis of the calcium and phosphorus content of developing and permanent human teeth. Ann Anat 189, 183–190. PubMed
Bell DA (1989) Functional anatomy of chameleon tongue. Zool Jb Anat 119, 313–336.
Bigi A, Foresti E, Gregorini R, et al. (1992) The role of magnesium on the structure of biological apatites. Calcif Tissue Int 50, 439–444. PubMed
Buchtova M, Zahradnicek O, Balkova S, et al. (2013) Odontogenesis in the Veiled Chameleon (Chamaeleo calyptratus). Arch Oral Biol 58, 118–133. PubMed
Burrage BR (1973) Comparative ecology and behaviour of Chamaeleo pumilis pumilis (Gemelin) and C. namaguensis A. Smith (Sauria: Chamaeleonidae). Ann S Aft Mus 61, 1–158.
Dauphin Y, Williams CT (2007) The chemical compositions of dentine and enamel from recent reptile and mammal teeth – variability in the diagenetic changes of fossil teeth. Cryst Eng Comm 9, 1252–1261.
Dauphin Y, Williams CT (2008) Chemical composition of enamel and dentine in modern reptile teeth. Mineral Mag 72, 247–250.
Edmund AG (1969) Dentition In: Biology of the Reptile (ed. Gans C.), pp. 117–200. London: Academic Press.
Enax J, Fabritius HO, Rack A, et al. (2013) Characterization of crocodile teeth: correlation of composition, microstructure, and hardness. J Struct Biol 184, 155–163. PubMed
Gaengler P (1991) Evolution of tooth attachment in lower vertebrates to tetrapods In: Mechanisms and Phylogeny of Mineralization in Biological Systems (eds Suga S, Nakahara H.), pp. 173–185. Berlin: Springer.
Gaengler P, Metzler E (1992) The periodontal differentiation in the phylogeny of teeth – an overview. J Periodontal Res 27, 214–225. PubMed
Galiova M, Kaiser J, Novotny K, et al. (2010) Investigation of the osteitis deformans phases in snake vertebrae by double‐pulse laser‐induced breakdown spectroscopy. Anal Bioanal Chem 398, 1095–1107. PubMed
Gnanamuthu CP (1930) The anatomy and mechanism of the tongue of Chamaeleon calcaratus . Proc Zool Soc Lond 1930, 467–486.
Herrel A, Redding CL, Meyers JJ, et al. (2014) The scaling of tongue projection in the veiled chameleon, Chamaeleo calyptratus . Zoology (Jena) 117, 227–236. PubMed
Kieser JA, Tkatchenko T, Dean MC, et al. (2009) Microstructure of dental hard tissues and bone in the Tuatara dentary, Sphenodon punctatus (Diapsida: Lepidosauria: Rhynchocephalia). Front Oral Biol 13, 80–85. PubMed
Le Drogoff B, Margot J, Chaker M, et al. (2001) Temporal characterization of femtosecond laser pulses induced plasma for spectrochemical analysis of aluminum alloys. Spectrochim Acta Part B, 56, 987–1002.
Lucas PW(1979) Basic principles of tooth design In: Teeth, Form, Function, Evolution. (ed. Kurten B.), pp. 154 New York: Columbia University Press.
McIntosh JE, Anderton X, Flores‐De‐Jacoby L, et al. (2002) Caiman periodontium as an intermediate between basal vertebrate ankylosis‐type attachment and mammalian ‘true’ periodontium. Microsc Res Tech 59, 449–459. PubMed
Mivart SG (1870) On the myology of Chamaelon parsonii . Proc Zool Soc Lond 1870, 850–890.
Ohazama A, Courtney JM, Sharpe PT (2004) Opg, Rank, and Rankl in tooth development: co‐ordination of odontogenesis and osteogenesis. J Dent Res 83, 241–244. PubMed
Osborn JW (1984) From reptile to mammals: evolutionary considerations of dentition with emphasis on tooth attachment. Symp Zool Soc Lond 52, 549–574.
Rieppel O (1981) The skull and jaw adductor musculature in chameleons. Rev Suisse Zool 88, 433–445.
Saffar JL, Lasfargues JJ, Cherruau M (1997) Alveolar bone and the alveolar process: the socket that is never stable. Periodontol 2000 13, 76–90. PubMed
Smith AJ, Lesot H (2001) Induction and regulation of crown dentinogenesis: embryonic events as a template for dental tissue repair? Crit Rev Oral Biol Med 12, 425–437. PubMed
So K‐KJ, Wainwright PC, Bennett AF (1992) Kinematics of prey processing in Chamaeleo jacksonii: conservation of function with morphological specialization. J Zool 226, 47–64.
Sodek J, McKee MD (2000) Molecular and cellular biology of alveolar bone. Periodontol 2000 98(24), 99–126. PubMed
Steinfort J, Driessens FC, Heijligers HJ, et al. (1991) The distribution of magnesium in developing rat incisor dentin. J Dent Res 70, 187–191. PubMed
Stuart‐Fox DM, Whiting MJ (2005) Male dwarf chameleons assess risk of courting large, aggressive females. Biol Lett 1, 231–234. PubMed PMC
Ten Cate AR (1994) Development of The Tooth and its Supporting Tissue. In: Oral histology: development, structure and function St. Louis: Mosby‐Year Book.
Tjaderhane L, Hietala EL, Larmas M (1995) Mineral element analysis of carious and sound rat dentin by electron probe microanalyzer combined with back‐scattered electron image. J Dent Res 74, 1770–1774. PubMed
Wiesmann HP, Tkotz T, Joos U, et al. (1997) Magnesium in newly formed dentin mineral of rat incisor. J Bone Miner Res 12, 380–383. PubMed
Young RA (1974) Implications of atomic substitutions and other structural details in apatites. J Dent Res 53, 193–203. PubMed
Zaher H, Rieppel O (1999) Tooth implantation and replacement in squamates, with special reference to mosasaurs lizards and snakes. Am Mus Novit 3271, 1–19.
Zoond A (1933) The mechanism of projection of the chameleon's tongue. J Exp Biol 10, 174–185.
X-ray microtomography-based atlas of mouse cranial development