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A Huysseune

Publications and source records attributed to A Huysseune.

15 recordsLinked to original sources

Fish dentitions as paradigms for odontogenic questions.

Bony fish, and in particular teleosts, represent a morphologically extremely diverse group of vertebrates, well suited to study certain problems in odontogenesis. In this article we address some questions that can benefit much from the use of fish dentitions as paradigms, such as endodermal participation in tooth formation and epithelial primacy in initiation events. Next, we highlight some results recently obtained in our laboratory with respect to two models, the zebrafish (Cyprinidae), and selected species of cichlids (Cichlidae). Finally, we pinpoint some questions that lend themselves admirably to be examined using fish models, such as the factors that control renewed initiation of teeth, and the relationship (or absence thereof) between Hox genes and tooth formation.

Animals↗

Tooth shape differences analyzed by biometric and morphometric approaches: a case study on two morphologically very similar lacustrine cichlid species.

Tooth shape is generally considered to be under strong genetic control, and highly species specific. It is therefore widely used for taxonomic studies. The tooth shape-based morphological classification of the Eretmodini (a tribe of closely related cichlids endemic to Lake Tanganyika), has, however, been shown to be in conflict with recent molecular data, which suggests the occurrence of parallel evolution. A detailed biometric and morphometric analysis of tooth shape has been undertaken for two genetic lineages of the taxon Eretmodus cyanostictus. The use of both landmark-based measurements and elliptic Fourier analysis reveals differences between both lineages and supports the molecular phylogeny. These differences further endorse the interpretation of parallel evolution. In addition, we here present a powerful tool for the analysis of tooth shape.

Animals↗

Developmental differences between cranial bones in the zebrafish (Danio rerio): some preliminary light and TEM observations.

To test whether cartilage bones and dermal bones, which belong to two different units of the vertebrate skeleton, have distinct developmental programs possibly reflected in a different molecular control of their ossification process, we currently investigate the development of some selected cranial bones in the zebrafish, Danio rerio. Here we present some light microscopical and ultrastructural findings with respect to the maxillary bone (a dermal bone that is edentulous in the zebrafish) and the basioccipital bone (a cartilage bone, i.e., with a perichondral phase followed by endochondral invasion). The two bones differ in (a) the area where matrix is first deposited--an unstructured extracellular domain in the former versus intermingling of bone matrix elements with cartilage matrix in the latter--and (b) the progression of ossification--continuously from an initium in the former versus through fusion of separate anlagen in the latter. These findings seem to support the hypothesis that the two types of bone have at least some distinctive features in their developmental programs.

Animals↗

A quantitative analysis of pharyngeal tooth shape in the zebrafish (Danio rerio, Teleostei, Cyprinidae).

To test whether successive replacement cycles in the pharyngeal dentition of the zebrafish, a polyphyodont vertebrate model organism, entail overall shape changes in the teeth, a qualitative and quantitative analysis was made of size and shape variables in the five ventral teeth. The following measurements were defined: tooth length, tooth height, neck-crown angle, cusp depth, and crown curvature. Ontogenetic changes in fish, ranging between 6 and 29 mm standard length (SL), were analysed by linear regressions on to SL. The teeth became significantly larger with growth of the fish, through successive replacements and cusp depth also increased over time. Neck--crown angle and crown curvature did not change over time. Position-dependent differences were analysed by Friedman ANOVA and Kendall concordance tests. Measurements differed significantly according to tooth position in the pharyngeal jaws. Tooth 1V was always the smallest, 3V the largest. The neck--crown angle and curvature of the crown increased from 1V to 5V. Cusp depth increased from 1V to 3V, and then decreased again. These results indicate that successive replacement cycles entail a size increase accompanied by shape changes apparently restricted to the crown. These quantitative data lay the basis for further descriptive and experimental studies of tooth shape in this model-species.

Analysis of Variance↗

Tooth succession in the zebrafish (Danio rerio).

To test whether the formation of replacement teeth in arbitrarily chosen zebrafish follows the same pattern as described for larval and young zebrafish of known age, dentitions of more than 90 animals of different ages and standard lengths were observed under the stereomicroscope. Only the teeth of the ventral tooth row (1V-5V) were considered. Statistical results (G-tests) suggested that tooth replacement does not occur randomly. The most common order of replacement can be represented as the formula 5V-2V-3V-1V-4V and counts for approximately 70% of the observed patterns. Initiation of replacement teeth at positions 4V and 5V is separated by a larger time interval than between any other combination. It is hypothesized that in older juveniles and adults, replacement teeth may be formed during three odontogenic waves.

Age Factors↗

Dynamics of tooth formation and replacement in the zebrafish (Danio rerio) (Teleostei, Cyprinidae).

We have used three-dimensional reconstructions from serial sections as well as cleared and stained specimens to infer patterning of the pharyngeal dentition throughout ontogeny in the zebrafish. Each pharyngeal tooth has been monitored from its initiation to its complete disappearance (resorption and shedding). We have identified tooth families and have studied the persistence of the pattern through successive replacements. Teeth arise in two seemingly independent clusters, a ventral and a dorsal cluster, with differing patterning features. The ventral cluster consists of one row of five teeth in which a tooth is first initiated in position four, and subsequent teeth in adjacent positions, posterior and anterior to it. Replacement teeth in odd and even positions are initiated simultaneously during successive odontogenic waves but differ in generation number according to the timing of appearance of the first-generation tooth, i.e., the founder of the tooth family. Up to four teeth of a single tooth family are simultaneously present in early juveniles of which two are usually "co-functional." The number of teeth per tooth family is reduced in older juveniles and adults, reflecting a slowing down of the replacement rate. The consistent way in which the pattern is established and maintained during ontogeny calls for research of the presence of specific molecular controls.

Animals↗

Development and fine structure of pharyngeal replacement teeth in juvenile zebrafish (Danio rerio) (Teleostei, Cyprinidae).

Teeth are commonly used model systems for the study of epithelial-mesenchymal interactions during organogenesis. We describe here the ultrastructural characteristics of developing pharyngeal replacement teeth in juvenile zebrafish, an increasingly important model organism for vertebrate development. Replacement teeth develop in close association with the dental organ of a functional tooth. Morphogenesis is well advanced prior to the start of cytodifferentiation. Fibrillar enameloid matrix is formed first, followed by the deposition of predentine. Initial mineralization of the enameloid proceeds quickly; maturation involves the presence of ruffled-bordered ameloblasts. Dentine mineralization is inotropic and is mediated by matrix vesicles. Woven-fibred attachment bone matrix is deposited before completion of dentine mineralization. Eruption of fully ankylosed teeth is a fast process and may involve degenerative changes in the pharyngeal epithelium. Mononucleated osteoclasts and clastic cells located in the pulp cavity intervene in tooth resorption prior to shedding. Structural differences with larval, first-generation zebrafish teeth include the presence of dentinal tubules and the absence of an electron-dense covering membrane. Part of these differences may relate to size differences of the teeth. Others, like the site of the replacement tooth bud, suggest that initiation may take place in already committed epithelium from the first initiation event in the larval stage.

Amelogenesis↗

Early development of the zebrafish (Danio rerio) pharyngeal dentition (Teleostei, Cyprinidae).

In order to build a reference system to assess ongoing in vitro and in situ hybridisation experiments on epithelial-mesenchymal interactions governing odontogenesis in the zebrafish, we describe here the generation of the pharyngeal dentition, and the histological development of teeth up to fourteen days post-fertilization, using serial semithin sections, handmade and computer-assisted reconstructions and transmission electron microscopy. The tooth pattern in larval zebrafish is generated in a predictable, and bilaterally symmetrical manner from shortly before hatching onwards. Characteristics related to tooth development and structure differ considerably from those seen in juvenile specimens and those described for other bony fishes. Particular features related to the cyprinid condition include the complex epithelial connectivity and the mode of attachment of the teeth.

Aging↗

Evolution of patterns and processes in teeth and tooth-related tissues in non-mammalian vertebrates.

The evolutionary links that exist between odontodes and organs that are phylogenetically related to them (teeth and scales) suggest the use of comparative approaches to study these structures. Part one of this review briefly introduces current ideas on how the pattern of odontodes and odontode-derived tissues has been established during evolution to yield the diversity of odontode-related organs currently observed in nature in the cranial and postcranial skeleton. This introductory survey is used to highlight aspects of the developmental processes underlying the formation of some of these organs and the resemblance their development bears to odontogenesis. Part two provides a concise survey of the diversity of tooth structure in the different classes of extant vertebrates, in particular with reference to enamel/enameloid and dentine structure, and tooth attachment. Against this background, the current state of knowledge is reviewed with regard to developmental mechanisms involved in non-mammalian odontogenesis. Common structure and similarities in development demonstrate that teeth and odontode derivatives should not be considered subjects of separate lines of research. On the contrary, results acquired in one of these fields are relevant to the other and may disclose model species that are relevant to studies on mammalian odontogenesis.

Animals↗

Phenotypic plasticity in the lower pharyngeal jaw dentition of Astatoreochromis alluaudi (Teleostei: Cichlidae).

The potentially molluscivorous cichlid fish Astatoreochromis alluaudi is known to exhibit a pronounced phenotypic plasticity in its pharyngeal jaw apparatus. Two phenotypes (wild-caught snail-eating specimens and specimens raised on soft food) were examined for differences in the number, size, shape, spacing and wear of functional teeth on the lower pharyngeal jaw. During growth, snail-eating specimens maintain tooth numbers but invest in teeth of a larger size (width and depth). In contrast, specimens fed a soft diet invest in more teeth, their size remaining unchanged except for the central, most posterior teeth. All changes in the dentition must be achieved through successive tooth generations. Serial microradiographs in the caudal area of the lower pharyngeal jaw, a region that is most significant in food processing, indicated that functional teeth in hard-food specimens more often show a successor below. This may be due to more time needed for larger replacement teeth to form and possibly to a shorter replacement cycle linked to the greater wear of the functional teeth. It is hypothesized that maintenance of tooth numbers and increase of tooth size in hard-food specimens is achieved by a one-for-one replacement and expansion of the tooth-bearing region and possibly by closer spacing of the teeth. Increase of tooth numbers in the soft-food specimens is probably achieved through the establishment of new tooth loci at the margins of the dentigerous area in addition to a one-for-one replacement.

Africa, Eastern↗

Development of cartilage and bone tissues of the anterior part of the mandible in cichlid fish: a light and TEM study.

The present paper presents ultrastructural details of chondrogenesis of Meckel's cartilage and of ossification of its associated peri- and parachondral bones in a teleost fish, the cichlid Hemichromis bimaculatus. We have distinguished four stages during chondrogenesis, each of which is characterized by specific cellular and matrix features: blastema, primordium, differentiated cartilage and cartilage surrounded by perichondral bone. The blastema is characterized by prechondroblasts and the lack of cartilage matrix; the primordium by chondroblasts and the onset of secretion of matrix of fibrillar and granular nature; differentiated cartilage is characterized by chondrocytes and larger amounts of typical hyaline cartilage matrix. Once perichondral bone is laid down, the chondrocytes show degenerative features but not true hypertrophy. Differentiation of the cartilage cells is attended with cytoplasmic changes indicative of an increasing secretory activity. There is a regional calcification of the cartilage matrix by fusion of calcospherites. Chondrogenesis of the symphyseal area is continuous with that of the rami but starts slightly later. Formation of perichondral bone at the cartilage surface is attended with the deposition of a transitional zone apparently containing a mixture of the two matrices. The role of the perichondral cells is discussed and it is proposed that they may contribute to the formation of the two matrices. The transitional zone may then result either from a diffusion process or from the simultaneous deposition of elements of the two matrices. Growth of the cartilage is argued to be largely the result of matrix secretion, except in the symphyseal area where appositional growth probably occurs until the region is completely covered by perichondral bone. This paper provides a basis for further studies on the developmental interactions between cartilage, bone and teeth during mandibular development in cichlids.

Animals↗

Bone and cartilage resorption in relation to tooth development in the anterior part of the mandible in cichlid fish: a light and TEM study.

This paper presents ultrastructural features of the contact region between particular tooth germs and Meckel's cartilage prior to, during, and after initial resorption of the perichondral bone and of the cartilage in the cichlids Hemichromis bimaculatus and Astatotilapia burtoni. Imminent resorption opposite such teeth is announced by the presence, in this region, of a particular cell type, considered to be a stage in the cytodifferentiation of osteoclasts. Slightly later, an osteoclast with typical ruffled border is seen to open a fenestra in the perichondral bone which surrounds Meckel's cartilage. Although the action of the osteoclast is directed primarily towards the bone, it may also affect, to a much lesser extent, the underlying uncalcified cartilage. Typically, fibroblast-like cells invade the resorption cavity along with the osteoclast; the tooth germ soon follows. Capillaries are seen to invade the cartilage only at a later stage when a large cavity has been established. It is proposed that the fibroblast-like cells may have a dual function: degradation of cartilage and deposition of new bone. Although these processes are normally limited to the area surrounding tooth germs at specific loci, tooth germs in other positions may sometimes be seen invade the cartilage. They do so either passively, because of the existence of such a cavity, or as a result of their own resorption-inducing activity. Whatever the mechanism, attachment bone is being deposited within the erosion cavity and on the surface of the exposed perichondral bone. The stimuli possibly eliciting resorption of Meckel's cartilage are discussed. It is hypothesized that pressure exerted by the growing tooth germ may stimulate the osteoblasts covering the bone surface and, in this way, provoke osteoclastic bone resorption.

Animals↗

Mechanisms of branchial cartilage growth in Astatotilapia elegans (Teleostei: Cichlidae).

The growth of the cartilaginous infrapharyngobranchial II (part of the upper pharyngeal jaws) in the cichlid fish Astatotilapia elegans was investigated in four successive early postembryonic stages. Total cell number, individual cell volumes, total cell, total matrix and total cartilage volume were accurately measured or calculated. The share of cell and matrix volume increase in the overall growth was calculated for each of the transitions. Matrix volume increase accounted for almost 60% of the overall rudiment increase. Non-hypertrophic cells and the matrix produced by them together accounted for about three quarters of the total cartilage volume increase. Zones with particular characteristics (cell orientation, cell shape, degenerative features, etc.) were distinguished in each of the four stages separately. The sequence of increasing mean cell volume between zones was interpreted as reflecting growth directions within the cartilage. Apposition probably largely contributed to the observed cell volume increase. Mean cell volume and mean matrix volume per cell showed a highly significant positive relation. Cell density showed a highly significant negative relation to both mean cell volume and mean matrix volume. Our results indicate that the area of hypertrophy and cartilage resorption may be established quite early in the rudiment before overt manifestation of these processes.

Animals↗

Late skeletal development at the articulation between upper pharyngeal jaws and neurocranial base in the fish, Astatotilapia elegans, with the participation of a chondroid form of bone.

This paper presents light-microscopical details of the late development of skeletal tissues at the joint between upper pharyngeal jaws (UPJs) and neurocranial base (parasphenoid and basioccipital bones) in the acellular-boned teleost Astatotilapia elegans. On each of the supporting elements, a bone tissue (AB) is deposited that is anomalous because of its retention of cells within the matrix. Later, this layer is gradually replaced by the anomalous large-celled chondroid kind of bone (CB). Both AB and CB probably grow by apposition from the overlying fibrous layer. Osteoblastlike cells secrete osteoid, which soon calcifies and traps the cells. As in young cellular membrane bone, cells in the AB have a wide, elongate shape and lie amidst sparse, calcified, bonelike matrix but lack a canalicular system. Later generations of enclosed cells have a more vesicular shape, with at least some cells remaining alive in the calcified matrix. Appositional growth of the chondroid bone at its articular side is matched from a certain stage onward by erosion at its basal side. On the upper pharyngeal jaws this resorption is clearly related to the development of new teeth. Although in older stages and adults the chondroid tissue resembles a secondary cartilage, the term chondroid bone (CB) was preferred because of (1) the continuing formation by osteoblastlike cells; (2) the staining affinities of its matrix with that of bone; and (3) its formation both on cartilage bone (the infrapharyngobranchials III-IV and basioccipital bone) and on membrane bone (the parasphenoid bone).

Age Factors↗

Chondroid bone on the upper pharyngeal jaws and neurocranial base in the adult fish Astatotilapia elegans.

Serial cross sections of several adult specimens of the cichlid Astatotilapia elegans were used to investigate the fate and structure of the chondroid bone on the articulation between upper pharyngeal jaws and neurocranial base. The tissue persists in the adult on the three elements on which it previously developed, i.e., infrapharyngobranchial III-IV, parasphenoid, and basioccipital bones. It consists of haphazardly arranged, large vesicular cells without a canalicular system, embedded in a matrix histologically indistinguishable from bone matrix. Except for a narrow zone at the distal side, it is mineralized throughout. As in younger stages, the fibrous covering of the chondroid bone forms the articular tissue proper on each of the three elements. Acellular bone, found at the basal margin of the chondroid bone, it is argued, does not result from endochondral replacement of the latter but rather from dermal ossification projecting from the marrow cavity. Although lacunae may be filled in this way with bone, true obliteration of cells does not occur, so that there is no metaplasia from chondroid bone to bone. The part played by the chondroid bone in the outgrowth of the joint apophyses is discussed.

Animals↗