Les amphibiens sont des vertébrés liés aux alternances entre la vie aquatique et la vie terrestre et aux alternances saisonnières. Le développement embryonnaire commence par une phase aquatique et se termine par une métamorphose qui donnera une forme juvénile terrestre pouvant rester dans le milieu aquatique chez certaines espèces retournées secondairement à la vie aquatique. Les cycles de reproduction sont régulés, entre autres, par les hormones hypophysaires: LH et FSH (gonadotropes) et PRL (prolactine). La régulation hydrominérale des vertébrés est également assurée par des hormones neurohypophysaires telles que l'arginine vasopressine (AVP), l'ocytocine (OT), l'arginine vasotocine (AVT), la mésotocine (MST) et l'isotocine (IST). Le but du travail effectué dans le cadre de cette thèse a été d'apporter quelques éléments de compréhension des liens pouvant exister entre la reproduction et la régulation hydrominérale. Les cycles de reproduction de Typhlonectes compressicauda sont soumis à des alternances saisonnières caractérisées par une saison des pluies et une saison sèche.Dans le présent travail nous avons mis en évidence les principales hormones impliquées dans la régulation de la balance hydrique (AVT, MST). Parallèlement, une étude précise de la structure des reins avec la mise en évidence des récepteurs de différentes hormones concernées a été menée. La mise en évidence par biochimie (western blot et dosage) des différentes hormones et de leurs récepteurs (immunohistochimie) a également été effectuée chez Xenopus laevis, espèce aquatique représentant un modèle d'étude conventionnel, de manière à apprécier l'implication de ces hormones lorsque l'animal termine sa métamorphose / The amphibians are vertebrates the cycle of life being related to both the alternations between aquatic and terrestrial phases and seasonal alternations. Embryonic development begins with an aquatic phase and completed with a metamorphosis, at the end of which terrestrial juveniles animals can persist in the aquatic environment in secondary aquatic species. The breeding cycles are regulated by the pituitary hormones: LH, FSH (gonadotropins) and PRL (prolactin). The hydromineral regulation of vertebrates is also ensured by neurohypophysial neurohormones such as arginine vasopressin (AVP), oxytocin (OT), vasotocin (AVT), mesotocin (MST), and isotocin (IST).The work in the context of this thesis was to bring some elements for understanding the relationships that may exist between the reproduction and hydromineral regulations.The reproductive cycles in Typhlonectes compressicauda are submitted to seasonal alternations characterized by a rainy season and a dry season. In the present work we highlighted the main hormones involved in the regulation of hydric balance in amphibians (AVT, MST). In parallel, a precise study of the structure of the kidneys with the identification of receptors of various hormones concerned, was performed. The identification of both various hormones and their receptors by biochemistry (Western blot, assay) and immunohistochemistry was also performed on Xenopus laevis, an aquatic species representing also a conventional model for the study, in way to appreciate the implication of these hormones when the animal completes its metamorphosis

Au cours de la métamorphose, les amphibiens subissent une réorganisation complète de leur anatomie et de leur physiologie. Chez Xenopus laevis le système locomoteur est un des plus affecté au cours de cette phase développementale, l’animal passant d’une nage ondulatoire à une nage appendiculaire. Cette transformation du mode locomoteur implique une réorganisation du réseau locomoteur central. Dans une première étude, nous avons mis en évidence que les muscles axiaux s’activent de manière bilatéralement alternée chez le têtard alors que les muscles équivalents chez l’adulte s’activent de manière synchrone au cours de la nage. Nous avons montré que ce nouveau patron d’activation musculaire, accompagné d’une synchronisation avec les muscles appendiculaires extenseurs, reposent principalement sur la mise en place de nouvelles projections propriospinales lombo-thoraciques. Ces résultats suggèrent l’existence d’un contrôle postural proactif au cours de la locomotion, reposant directement sur le CPG des membres postérieurs. Dans une deuxième étude, nous nous sommes intéressés à l’influence d’un déséquilibre des afférences vestibulaires sur le développement du réseau locomoteur spinal au cours de la métamorphose. Pour cela nous avons réalisé une suppression unilatérale des organes vestibulaires avant ou après la métamorphose. Dans les deux cas, cette lésion aigue génère d’importants troubles locomoteurs et posturaux. Nous avons montré que la lésion chronique au cours de la métamorphose entraîne une modification ipsi-lésionnelle du développement du réseau locomoteur lombo-thoracique, de manière concomitante à une compensation comportementale. De façon intéressante, cette plasticité développementale ainsi que la compensation des troubles locomoteurs sont absentes chez les animaux lésés au stade adulte. Ces résultats suggèrent que les informations sensorielles sont un facteur déterminant pour le développement du réseau locomoteur spinal. Enfin, dans une troisième étude, nous avons analysé le développement du réseau locomoteur supra-spinal et en particulier les propriétés de déclenchement et de contrôle de la région locomotrice mésencéphalique (MLR). Nous avons mis en évidence l’existence fonctionnelle des deux noyaux de cette structure, le noyau pédonculopontin (PPN) et le noyau latérodorsal du tegmentum (LDT) tout au long de la métamorphose du xénope, ainsi qu’une fréquence d’activation optimale de 10-20 Hz pour le PPN. / Throughout the course of metamorphosis, amphibians undergo a complete anatomical and physiological reorganization. In Xenopus laevis, the locomotor system is one of the most affected during this developmental phase where the animal passes from undulatory swimming to limb-based propulsion. This transformation implies a parallel reorganization of the central locomotor network. In an initial study we showed that axial muscles which are activated in bilateral alternation in tadpoles mature to dorsal muscles that are synchronously active during adult locomotion. We found that this new pattern, accompanied by coordination of dorsal and hindlimb muscle activities, is principally sustained by the development of new propriospinal lumbo-thoracic projections, suggesting proactive postural control coming from the hindlimb CPG during ongoing locomotion. In a second study, we examined the influence of disequilibrium in vestibular inputs on the metamorphic development of the spinal locomotor network. To induce this sensory asymmetry we performed unilateral removal of vestibular end organs either before or after metamorphosis. Acutely, in both cases, the lesion induced dramatic postural and locomotor changes. Chronically, the lesion altered the metamorphic development of the lumbo-thoracic network on the lesioned side, concomitantly with compensation for locomotor defects. Interestingly, animals lesioned after metamorphosis neither compensated nor expressed this developmental spinal plasticity. Altogether, these results suggest that descending sensory inputs are crucial cues for the development of the spinal locomotor network. Finally, we studied the metamorphic development of the supra-spinal network, focusing our attention on the locomotor triggering and control properties of the mesencephalic locomotor region (MLR). We showed that both subparts of this structure, the laterodorsal tegmentum (LDT) and the pedunculopontine (PPN) nuclei, are present and functional during the entire period of metamorphosis and that the PPN has an optimal activation frequency of 10-20 Hz.

Triclosan (TCS) and triclocarban (TCC) are antimicrobials found in U.S. surface waters. This dissertation assessed the effects of TCS and TCC on early development and investigated their potential to bioaccumulate using Xenopus laevis as a model. The effects of TCS on metamorphosis were also investigated. For 0-week tadpoles, LC50 values for TCS and TCC were 0.87 mg/L and 4.22 mg/L, respectively, and both compounds caused a significant stunting of growth. For 4-week tadpoles, the LC50 values for TCS and TCC were 0.22 mg/L and 0.066 mg/L; and for 8-week tadpoles, the LC50 values were 0.46 mg/L and 0.13 mg/L. Both compounds accumulated in Xenopus. For TCS, wet weight bioaccumulation factors (BAFs) for 0-, 4- and 8-week old tadpoles were 23.6x, 1350x and 143x, respectively. Lipid weight BAFs were 83.5x, 19792x and 8548x. For TCC, wet weight BAFs for 0-, 4- and 8-week old tadpoles were 23.4x, 1156x and 1310x. Lipid weight BAFs were 101x, 8639x and 20942x. For the time-to-metamorphosis study, TCS showed an increase in weight and snout-vent length in all treatments. Exposed tadpoles metamorphosed approximately 10 days sooner than control tadpoles. For the hind limb study, although there was no difference in weight, snout-vent length, or hind limb length, the highest treatment was more developed compared to the control. There were no differences in tail resorption rates between the treatments and controls. At relevant concentrations, neither TCS nor TCC were lethal to Xenopus prior to metamorphosis. Exposure to relatively high doses of both compounds resulted in stunted growth, which would most likely not be evident at lower concentrations. TCS and TCC accumulated in Xenopus, indicating that the compound has the potential to bioaccumulate through trophic levels. Although TCS may increase the rate of metamorphosis in terms of developmental stage, it did not disrupt thyroid function and metamorphosis in regards to limb development and tail resorption.

Regulation of size and growth is a fundamental problem in biology and often closely related to functionality and fitness. A prominent example is the mitotic spindle, whose size needs to be perfectly tuned to ensure proper chromosome segregation during cell division. It is known that spindle size generally scales with cell volume, most likely as a result of limiting components. However, this relation breaks down in very large cells where spindles have a maximum size. How the size and microtubule mass are set and why spindles show an upper size limit in large cells is still not understood. Spindles mainly consist of highly dynamic short microtubules that turn over very quickly in comparison to the lifetime of the entire structure. Thus, microtubules need to be constantly created throughout the spindle, a process called nucleation. Understanding the role of microtubule nucleation in setting the size of spindles is limited by the fact that little is known about the rate, distribution, and regulation of microtubule nucleation in these structures. This is partly due to the lack of methods to measure microtubule nucleation in spindles. During this work, I developed an assay based on laser ablation to probe microtubule nucleation in monopolar spindles assembled in Xenopus laevis egg extract. Using this new method in combination with quantitative microscopy, I found that microtubule nucleation in these structures is spatially regulated. Furthermore, I observed that nucleation is stimulated by pre-existing microtubules leading to new microtubule growth in their physical proximity. Combining my experimental results on nucleation with theory and further biochemical perturbations, I show that this autocatalytic nucleation mechanism is limited by the availability of active nucleators. In spindles, the amount of active nucleators decreases with distance from the chromosomes. Thus, this mechanism provides an upper limit to spindle size even when resources are not limiting.

Mitochondria from Xenopus laevis and Ambystoma mexica- num embryos between fertilization and the beginning of feeding were studied: the former with respect to metabolic behaviour, enzyme pattern and carrier activity, and the latter with respect to morphological parameters. The metabolic behaviour of mitochondria was studied by assessing the rates of oxygen uptake in presence of various substrates. The rates of oxidation of most substrates change during development. The only substrate to be readily metabolized is glutamate (in presence of malate), whose rate of oxidation presents a peak during gastrulation and declines during larval development. The high rate of oxidation of glutamate and a high aspartate aminotransferase activity indicate that the glutamate- aspartate cycle may be predominant in early embryonic mitochondria. The activity of enzymes from the matrix, the inner membrane and the outer membrane were studied. During early development activities of enzymes in the various compartments change independently of each other. Furthermore, enzymes within one compartment may vary independently. Measurements of carrier activity reveal that the carrier for dicarboxylic acids displays a high activity before gastrulation and decreases thereafter, while the tricarboxylic acid, pyruvate and glutamate/OH carriers show the opposite pattern of change, their activities being low or undetectable during early development. This implies that a mitochondrial differentiation takes place ' during development, beginning at gastrulation when the first differentiated cells appear. In order to correlate mitochondrial and cellular differentiation, morphological parameters of mitochondria from undifferentiated and differentiated cells - Ruffini cells and epidermal cells - were analyzed. Mitochondria from the differentiated cells are significantly different from those in undifferentiated cells. Thus the processes of cell differentiation are accompanied by morphological and biochemical differentiation of the mitochondria. / <p>Diss. (sammanfattning) Umeå : Umeå universitet, 1981, härtill 5 uppsatser</p> / digitalisering@umu

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The heat shock or stress response is a transient response to stressful stimuli that protects vital cellular proteins from damage and irreversible aggregation. Heat shock proteins (Hsps) are molecular chaperones that bind to unfolded protein and inhibit their aggregation, thereby maintaining their solubility until they can be refolded to their native conformation. Hsp47 is an endoplasmic reticulum (ER)-resident protein that serves as a molecular chaperone during collagen production. Collagen is the major class of insoluble fibrous protein found in the extracellular matrix and in connective tissues. It is the single most abundant protein of the animal kingdom; at least 14 different forms exist, each with distinct structures and binding properties. The various types of collagen all possess protein regions with the distinct triple helical conformation. This complex physical structure requires very organized assembly and HSP47 has been established as an integral component of this process for collagen types I-V. Most of the previous studies examining the expression and function of hsp47 have been conducted with mammalian cultured cells. The present study represented the first investigation of the expression of hsp47 in the poikilothermic vertebrate, <i>Xenopus laevis</i>. Full-length <i>Xenopus</i> hsp47 nucleotide and amino acid sequences were obtained from Genbank and compared with hsp47 from chicken, mouse, rat, human and zebrafish. <i>Xenopus</i> HSP47 protein had an identity of approximately 77% with chicken, 73% with mouse, 72% with rat and human, and 70% with zebrafish. Most of the sequence identity between HSP47 from all investigated organisms occurred centrally in the amino acid sequence and in several carboxyl terminal regions. Three key features were conserved between HSP47 proteins from most species investigated: a hydrophobic leader sequence, two potential glycosylation sites and the ER-retention signal, RDEL. A partial cDNA clone encoding <i>Xenopus</i> hsp47 was obtained from the American Type Culture Collection (ATCC) and used to generate hsp47 antisense riboprobe for the purpose of investigating hsp47 mRNA accumulation in <i>Xenopus</i> A6 kidney epithelial cells and embryos. Northern blot analysis detected hsp47 mRNA constitutively in A6 cells. The expression pattern for hsp47 mRNA was compared with two other <i>Xenopus</i> heat shock proteins that have been previously characterized in our laboratory: hsp70, a cystolic/nuclear hsp and BiP, an ER-resident hsp. The results of hsp47 mRNA accumulation in A6 cells suggested that the expression pattern for <i>Xenopus</i> hsp47 was unique but, with respect to some stressors, resembled that of a cytosolic hsp rather than an ER-resident hsp. HSP47 protein levels were also examined in A6 cells. Heat shock, sodium arsenite and b-aminopropionitrile fumerate treatments enhanced hsp47 accumulation. In some experiments, western blot analysis revealed the presence of two closely sized protein bands. It is possible that minor differences in HSP47 protein size may be due to post-translational modification, namely phosphorylation or glycosylation. The present study also examined the accumulation and spatial pattern of hsp47 mRNA accumulation during <i>Xenopus laevis</i> early development. Hsp47 was constitutively expressed throughout <i>Xenopus</i> early development. Constitutive levels of hsp47 mRNA in unfertilized eggs, fertilized eggs and cleavage stage embryos indicated that these transcripts were maternally inherited. Constitutive hsp47 mRNA accumulation was enhanced in neurula and tailbud embryos compared to earlier stages. This finding may be explained by the shift towards organogenesis during these stages. Whole mount <i>in situ</i> hybridization revealed hsp47 message along the dorsal region of the embryo, in the notochord and somites, as well as in the head region including the eye vesicle. Hsp47 mRNA induction in <i>Xenopus</i> embryos was also examined in response to heat shock. Hsp47 mRNA accumulated in response to heat shock immediately following the midblastula transition (MBT). In tailbud stages, hsp47 mRNA accumulated in the notochord, somites and head region. Northern blot analysis and whole mount <i>in situ</i> hybridization results revealed an expression pattern that coincided well with the development of collagen-rich tissues thereby substantiating the proposed role of HSP47 as a procollagen molecular chaperone.

No description available.

No description available.

No description available.