Jacqueline Géraudie

Old questions, new tools, and some answers to the mystery of fin regeneration†

Pluridisciplinary approaches led to the notion that fin regeneration is an intricate phenomenon involving epithelial–mesenchymal and reciprocal exchanges throughout the process as well as interactions between ray and interray tissue. The establishment of a blastema after fin amputation is the first event leading to the reconstruction of the missing part of the fin. Here, we review our knowledge on the origin of the blastema, its formation and growth, and of the mechanisms that control differentiation and patterning of the regenerate. Our current understanding results from studies of fin regeneration performed in various teleost fish over the past century. We also report the recent breakthroughs that have been made in the past decade with the arrival of a new model, the zebrafish, Danio rerio, which now offers the possibility to combine cytologic, molecular, and genetic analyses and open new perspectives in this field. Developmental Dynamics 226:190–201, 2003.

Gene Expression during Amphibian Limb Regeneration

Limb regeneration in adult urodeles is an important phenomenon that poses fundamental questions both in biology and in medicine. In this review, we focus on recent advances in the characterization of the regeneration blastema at cellular and molecular levels and on the current understanding of the molecular basis of limb regeneration and its relationship to development. In particular, we discuss (i) the spatiotemporal distribution of genes and gene products in the mesenchyme and wound epidermis of the regenerating limb, (ii) how growth is controlled in the regeneration blastema, and (iii) molecules that are likely to be involved in patterning the regenerating limb such as homeobox genes and retinoids.

Fine structure of regenerating scales and their associated cells in the cichlid Hemichromis bimaculatus (Gill)

SummaryScale regeneration has been studied in Hemichromis bimaculatus. The removed scale, which serves as a control, is covered by its surrounding scleroblasts as can be seen with scanning electron microscopy. Subsequently, during regeneration, a population of scleroblasts arises in the empty dermal pocket as shown with transmission electron microscopy. At first, an elongated papilla of regeneration forms, probably from the differentiation of dermal fibroblasts. A scale anlage composed of the osseous layer appears in the middle of the papilla, which becomes a regenerating bag. All the surrounding large scleroblasts are involved in scale formation, although later three populations of scleroblasts specialize according to their location around the scale. Superficial scleroblasts flatten when the final thickness of the osseous layer of the scale is attained; the deep scleroblasts are responsible for the formation of the basal plate whereas marginal scleroblasts increase the diameter of the osseous layer of the scale.During scale regeneration, scleroblasts are more numerous and larger than during scale ontogenesis. In particular, deep scleroblasts form a columnar epithelium when the basal plate is laid down, a feature which is not found during scale ontogenesis. Moreover, the regenerated basal plate exhibits an orthogonal “plywood” arrangement that is never seen in the embryonic scale where the “plywood” is of the intermediate type.

Open finger tip healing and replacement after distal amputation in Rhesus monkey with comparison to limb regeneration in lower vertebrates

SummaryThe left thumbs and great toes of three 81/2 month old Rhesus monkeys (Macaca mulatta) were amputated in guillotine fashion one millimeter distal to the base of the nail and allowed to heal by the conservative open wound method. Healing occurred in seven to ten days in these small digits. Each of the thumbs and toes grew back with some blunting and shortening of the digit tips, but were functional. The new structures were cosmetically pleasing as in the human instances. The nails grew essentially to normal size and shape supported by the remaining portions of the distal phalanges. Histological studies showed no evidence of blastema formation such as is observed in the regenerating limb of the Urodele (newt) taken as the comparative representative. The possibility of improving the regrowth is discussed against the background of our knowledge of the importance of nerve during limb regeneration in lower vertebrates.

Elastoidin actinotrichia in coelacanth fins: A comparison with teleosts

In this work, we present the first ultrastructural evidences of actinotrichia in the Coelacanth Latimeria. We describe its actinotrichia with the electron microscope (SEM and TEM) and compare their structure to Teleost actinotrichia. Both elements present similar fine structure, i.e. a periodic cross-striation of 60-65 nm; the plesiomorphic character of actinotrichia is discussed in Osteichthyes.

Comparison of even‐skipped related gene expression pattern in vertebrates shows an association between expression domain loss and modification of selective constraints on sequences

SUMMARY The even‐skipped related genes (evx) encode homeodomain‐containing transcription factors that play key roles in body patterning and neurogenesis in a wide array of Eumetazoa species. It is thought that the genome of the last common ancestor of Chordata contained a unique evx gene linked to a unique ancestral Hox complex. During subsequent evolution, two rounds of whole genome duplication followed by individual gene losses gave rise to three paralogs: evx1, evx2, and eve1. Then, eve1 was maintained in Actinopterygii lineage but not in Tetrapoda. To explain this discrepancy, we examined the expression patterns of the evx1 homologue, Xhox3, in Xenopus laevis and that of evx1 and eve1 in Danio rerio. We show here that Xhox3 is expressed in a manner that closely reflects the inferred expression pattern of the evx1 gene in the last common ancestor of Vertebrata (i.e., in gastrula, the central nervous system, the posterior gut, and the tip of the growing tail). Zebrafish evx1 and Xenopus Xhox3 are expressed in homologous cell lineages of the central nervous system and of the posterior gut, but evx1 was undetectable in the gastrula and the tail bud. Strikingly, eve1 is the only evx gene of zebrafish to be expressed in these two latter regions. Thus, the ancestral expression pattern of evx1 in vertebrates appears to have been distributed between evx1 and eve1 in zebrafish. We propose that evx1 and eve1 underwent a complementary loss of expression domain in zebrafish that allowed the maintenance of the two paralogs in accordance with the duplication‐degeneration‐complementation model. It is important to note that, in zebrafish, Evx1 and Eve1 have lost most of the protein domain upstream of the homeodomain. In addition, Eve1 has accumulated substitutions in positions that are highly conserved in all other Evx proteins. Thus, the reduction of the expression domain of both evx1 and eve1 in zebrafish appears to be associated with the modification of constraints on the protein sequences, allowing the shortening of both genes and an accelerated substitution rate in eve1.

Posterior hoxa genes expression during zebrafish bony fin ray development and regeneration suggests their involvement in scleroblast differentiation

Expression of two zebrafish developmental posterior hoxa genes, hoxa11b and hoxa13b, was studied by in situ hybridization during pectoral and caudal fin development and regeneration. Expression was restricted to cells of the bony rays region. During fin development, molecular cytological analysis revealed that a subpopulation of mesenchymal cells expressed these two hoxa genes during their early differentiation in the subapical region of the developing ray. These cells were identified as differentiating dermal bone making cells (scleroblasts). During fin regeneration, hoxa11b and hoxa13b genes are both induced in undifferentiated cells of the distalmost blastema region (DMB) and the proliferating zone (PZ) and later in differentiating bone-forming cells. In addition, the transient regionalization of the hoxa13b expression pattern in differentiated bone-forming cells along the proximodistal axis of the regenerating ray suggests that hoxa13b could participate in ray patterning. This study is the first to establish a correlation between hoxa gene expression and dermal bone cell differentiation.

Structure and comparative morphology of camptotrichia of lungfish fins

The present work is devoted to the organization and ultrastructure of the fin rays or camptotrichia of two living Dipnoi (lungfishes) Protopterus and Neoceratodus. In both species, these rods have a dual structure: only the superficial region facing the stratified epidermis is mineralized while the deep one is made of a dense unmineralized network of collagen fibrils forming a permanent pre-osseous tissue. Only the camptotrichia of Neoceratodus is made of cellular bone. This study confirms the structural peculiarities of these camptotrichia when compared to the dermal skeleton of the Actinopterygii constituted by the bony lepidotrichia and the actinotrichia. These results are discussed and compared to fossil dipnoan fin rays.

THE ORIGINS OF SPINAL GANGLIA IN THE AMPHIBIAN TAIL

Sensory ganglia of the amphibian tail differ from those of the trunk with regard to developmental pattern and ability to regenerate. We set out to examine tail ganglion formation during normal development and regeneration. Ganglion ontogenesis and regeneration in the tail follow a similar sequence beginning with ventral root outgrowth, formation of anlagen whose cells divide and go on to form ganglion neurons and glia and the later appearance of dorsal roots. Because there is no classical neural crest the source of the anlagen cells is not entirely clear. Our findings suggest that cells forming the regenerating ganglion migrate from the ventrolateral part of the regenerating spinal cord, whereas those of the embryonic and larval tail probably come from the tail bud.

The effect of electrical stimulation of brachiospinal nerves on protein synthesis in the forelimb regenerate of the newt

Abstract Electrical stimulation of brachiospinal nerves elevates protein synthesis in the blastema of the regenerating newt forelimb by 20% at 6 h post-stimulation. Restimulation 48 h after the initial stimulation produces exactly the same increase. Stimulation of axotomized brachiospinal nerves does not result in an elevation of blastemal protein synthesis but rather, after 48 h, a decrease similar to that found in non-stimulated, denervated blastemas.