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Étude de la régulation des canaux potassiques ROMK1 par un antidiabétique, la rosiglitazone implication des PPARgammaAit Benichou, Siham January 2011 (has links)
Les thiazolidinediones (TZDs) sont des médicaments antidiabétiques (agonistes des récepteurs nucléaires de type PPAR[gamma]) utilisés au cours des dix dernières années pour le traitement du diabète de type II. Malheureusement leur utilisation peut provoquer, chez certains patients, une rétention accrue de fluides et une formation d?oedèmes rénaux. Des études récentes suggèrent l'implication d'un canal sodique épithélial (ENaC), exprimé au niveau du tubule collecteur rénal, dans ces effets secondaires. En effet, la stimulation des PPAR[gamma] par les TZDs activent les canaux sodiques épithéliaux probablement via l'expression et l'activation de SGK1 (Serum and Glucocorticoid-regulated Kinase 1). Sachant que les transports des ions sodiques et potassiques sont étroitement liés au niveau rénal, notre objectif est de déterminer si les TZDs seraient impliqués dans la régulation des canaux potassiques (ROMK1). Nous montrons qu'en traitant les ovocytes de xénopes exprimant ROMK et PPAR[gamma], avec un TZDs comme la rosiglitazone (RGZ), le courant potassique mesuré par voltage-clamp (TEVC) est augmenté de deux fois. Cette augmentation est bloquée par l'utilisation d'un antagoniste de PPAR[gamma], le GW9662. Nous démontrons aussi l'implication de SGK1 dans la régulation de l'activité des canaux ROMK1 d'une part en mutant son site de phosphorylation sur ROMK1 (sérine 44) et d'autre part en utilisant son inhibiteur, GSK. Finalement les expériences d'immunofluorescences ont montré un recrutement de ROMK1 à la membrane des ovocytes traités à la RGZ. L'ensemble des données présentées dans ce travail suggère que la RGZ augmente le courant potassique en augmentant l'expression de SGK1.
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Estudio comparativo de corrientes totales de cloruro provenientes de membrana apical del sinciciotrofoblasto placentario humano normal y preeclámptico trasplantado a ovocitos de Xenopus laevis.Cruz Chomón, Carlos, Muñoz Zúñiga, Cristián January 2004 (has links)
El transporte existente entre la madre y feto es vital para el desarrollo de éste. La preeclampsia (PE) es una enfermedad que afecta múltiples funciones, entre ellas la de transporte. Hasta la fecha se han realizado pocos estudios sobre las alteraciones del transporte en la placenta con PE. El objetivo del presente estudio es comparar las corrientes totales en el ovocito de Xenopus laevis transplantado con membrana apical (MVM) proveniente de Sincicitrofoblasto (STP) normal y preeclámptico, donde el responsable de estas corrientes es el maxi-canal de cloruro, para así contribuir a establecer un modelo de transporte transplacentario en el embarazo normal y sus alteraciones en la preeclampsia. Se obtuvieron corrientes superiores en ovocitos inyectados con MVM preeclámptica, seguidas por las corrientes evocadas en ovocitos inyectados con MVM normal y las más bajas corrientes fueron obtenidas por los controles, evidenciando incorporación funcional de los canales exógenos y sugiriendo una alteración en los canales provenientes de la placenta preeclámptica.
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Implication de la O-GlcNAc dans la régulation de la transition G2/M ovocytaire et l'embryogenèse précoce chez Xenopus Laevis / Implication of O-GlcNAc in the regulation of the oocyte G2/M transition and the early embryogenesis in Xenopus laevisDehennaut, Vanessa 30 October 2008 (has links)
La O-GlcNAc est une glycosylation dynamique, résidente du cytosol et du noyau, participant à la régulation de processus biologiques tels que le cycle cellulaire et l'embryogenèse. Nos travaux ont porté dans un premier temps sur le contrôle par la O-GlcNAc de la reprise méiotique de l'ovocyte deXenopus laevis, processus analogue à la transition G2/M du cycle cellulaire. Cette transition G2/M est caractérisée par l'activation simultanée du M-phase Promoting Factor, facteur universel d'entrée en phase M et de la voie MAPK-Erk2, et par une augmentation du niveau de O-GlcNAc. Nous avons démontré que cette augmentation de O-GlcNAc était primordiale pour la reprise méiotique ovocytaire puisque l'inhibition de l'OGT, l'enzyme transférant le résidu de GlcNAc, empêche la transition G2/M de l'ovocyte alors que sa surexpression accélère ce phénomène. Nous avons identifié 24 protéines dont le niveau de O-GlcNAc augmente au cours de la reprise méiotique dont des protéines du cytosquelette, la kinase erk2, la phosphatase PP2A, des enzymes de la glycolyse et des protéines ribosomales. Nous avons également entrepris l'étude des variations de O-GlcNAc, d'OGT et d'UDP-GlcNAc au cours de l'ovogenèse et de l'embryogenèse précoce chez Xenopus laevis et avons montré que la dynamique de la O-GlcNAc était complexe tout au long de ces deux processus. Notamment, nous avons observé une diminution drastique et transitoire de la O-GlcNAc au début de la gastrulation suggérant une implication de la glycosylation dans les phénomènes de migration cellulaire caractéristiques de cette étape du développement mettant en place les trois feuillets embryonnaires à l'origine de tous les tissus de l'adulte. / O-GlcNAc is a dynamic and reversible post-translational modification found within the cytosol and the nucleus that take part in the regulation of many cellular processes among which cell cycle and embryogenesis. First, our works have focused on the study of O-GlcNAc implication in the control of Xenopus laevis oocyte meiotic resumption, a process analogous to the G2/M transition of the cell cycle. This G2/M transition is characterized by the simultaneous activation of the M-phase Promoting Factor, the universal regulator of the M-Phase entry and of the MAPK-Erk2 pathway but also by a sudden increase in the oocyte O-GlcNAc content. We have demonstrated that this O-GlcNAc increase was essential for meiotic resumption since the inhibition of OGT, the enzyme transferring the O-GlcNAc, prevents the oocyte G2/M transition whereas OGT overexpression accelerates this process. We identified 24 proteins that O-GlcNAc modification increases during meiotic resumption among which cytoskeletal proteins, the kinase erk2, the phosphatase PP2A, several glycolysis enzymes and sorne ribosomal proteins. Second, we have undertaken the study of O-GlcNAc, OGT and UDP-GlcNAc variations during the oogenesis and the early development of Xenopus laevis and we showed that the O-GlcNAc dynamism is intricate from the Xenopus oogenesis to embryogenesis. ln particular, we observed a drastic and transitory O-GlcNAc decrease at the onset of gastrulation, suggesting a role for O-GlcNAc in the regulation of cell migration characteristic of this stage of development since it permits the generation of the three germ layers, precursors ofthe whole adult tissues.
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Caracterización de las corrientes totales presentes en membrana basal de sinciciotrofoblasto placentario humano transplantado en ovocitos de Xenopus lavéisMadrid Campos, Gonzalo Javier January 2010 (has links)
Memoria para optar al Título Profesional de Médico Veterinario / El sinciciotrofoblasto presenta una membrana apical y una membrana basal, que constituyen la principal barrera para el intercambio materno fetal.
El cloruro (Cl-) es el principal ión extracelular y su paso através de la membrana apical ha sido ampliamente estudiado. Sin embargo, en la membrana basal el transporte de cloruro ha sido poco estudiado. El presente trabajo es el primero en describir las vías conductivas de cloruro existentes en la membrana basal (MB) del sinciciotrofoblasto trasplantado a ovocitos de Xenopus leavis a través del método de Voltage clamp.
Al transplantar MB a ovocitos de Xenopus Laevis, estos muestran un aumento de corrientes de al menos 3 veces en comparación a ovocitos controles y un aumento de conductancia de cuerda a 40 mV de 5,9 μS promedio. Además a 30 mV las corrientes exógenas disminuyeron en un 51,8% al agregar ácido 4,4'-diisotiocianatoestilbeno-2,2'-disulfónico (DIDS) y en un 52,8% al agregar ácido difenilamina-2-carboxílico (DPC), ambos conocidos bloqueadores de canales de Cl-. Estos datos demuestran la presencia vías conductivas para Cl- en la MB del sinciciotrofoblasto placentario humano / Financiamiento: Proyecto Fondecyt 1070695
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Caracterización de corrientes de cloruro en sinciciotrofoblasto humano proveniente de placentas con restricción de crecimiento intrauterinoMorales Toro, Bárbara Paz January 2011 (has links)
Memoria para optar al Título Profesional de Médico Veterinario / El sinciciotrofoblasto placentario (hSTB) constituye la principal barrera para el intercambio materno fetal.
Es de vital importancia que se lleve a cabo un adecuado transporte de solutos y nutrientes para que el feto pueda desarrollarse de forma normal. La Restricción de Crecimiento Intrauterino (RCIU) es la incapacidad del feto para alcanzar su potencial de crecimiento, una posible causa podría ser alteraciones en el transporte a
través del hSTB, ya que se han reportado cambios en cuanto a funcionalidad y expresión de algunos
transportadores en esta patología, sin embargo, no se ha estudiado mayormente lo que ocurre con un tipo de proteínas de transporte denominadas canales iónicos. En particular, es de importancia entender lo que ocurre
con el Maxi-canal de Cl⁻, ya que se ha visto que éste muestra alteraciones en sus características biofísicas en
otra patología del embarazo, la Preeclampsia. El objetivo del presente estudio fue caracterizar las corrientes de
Cl⁻ en el ovocito de Xenopus laevis trasplantado con membrana apical (MVM) proveniente de hSTB con RCIU, a
través de la técnica de Voltage Clamp. Las corrientes provenientes de ovocitos inyectados fueron
significativamente mayores que las obtenidas de ovocitos controles sin inyectar, evidenciando la incorporación
funcional de los canales exógenos provenientes de MVM RCIU. Estas corrientes exógenas fueron sensibles a
DIDS, un conocido bloqueador de canales de Cl⁻, el cual disminuyó las corrientes de manera voltaje dependiente, 45 % a -100 mV y 78 % a +40 mV, sugiriendo que las corrientes exógenas fueron principalmente
de Cl⁻. En cuanto a las corrientes evocadas en ovocitos inyectados con MVM normal, no fueron
significativamente distintas de las corrientes provenientes de MVM RCIU. Por otro lado, el bloqueador DIDS
(ácido 4,4-diisotiocianatostilbeno-2,2 disulfónico) mostró su efecto sólo a potenciales positivos, disminuyendo
las corrientes en un 36 % a +40 mV, siendo también voltaje dependiente, pero en menor magnitud / Proyecto FONDECYT 1070695
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Analyse der Kernhüllenbildung am Modellsystem Xenopus laevis / Studying nuclear envelope assembly in the cell-free system derived from Xenopus laevis eggsVollmar, Friederike Lara Veronika January 2008 (has links) (PDF)
Die Kernhülle ist eine hoch spezialisierte Membran, die den eukaryotischen Zellkern umgibt. Sie besteht aus der äußeren und der inneren Kernmembran, die über die Kernporenkomplexe miteinander verbunden werden. Die Kernhülle reguliert nicht nur den Transport von Makromolekülen zwischen dem Nukleoplasma und dem Zytoplasma, sie dient auch der Verankerung des Chromatins und des Zytoskeletts. Durch diese Interaktionen hilft die Kernhülle, den Zellkern innerhalb der Zelle und die Chromosomen innerhalb des Zellkerns zu positionieren, und reguliert dadurch die Expression bestimmter Gene. In höheren Eukaryoten durchlaufen sowohl die Kernhülle, als auch die Kernporenkomplexe während der Zellteilung strukturelle Veränderungen. Zu Beginn der Mitose werden sie abgebaut, um sich am Ende der Mitose in den Tochterzellen erneut zu bilden. Die molekularen Mechanismen, die zum Wiederaufbau der Kernhülle führen, sind kaum geklärt. Ein geeignetes System, um bestimmte Ereignisse bei der Kernhüllenbildung zu untersuchen, liefert das zellfreie System aus Xenopus Eiern und Spermienchromatin (Lohka 1998). Es konnte bereits früher gezeigt werden, dass es im Eiextrakt von Xenopus laevis mindestens zwei verschiedene Vesikelpopulationen gibt, die zur Bildung der Kernhülle beitragen. Eine der Vesikelpopulationen bindet an Chromatin, fusioniert dort und bildet eine Doppelmembran. Die andere Vesikelpopulation bindet an die bereits vorhandene Doppelmembran und sorgt für die Ausbildung der Kernporenkomplexe. Ziel dieser Arbeit war es, diese beiden Membranfraktionen zu isolieren und zu charakterisieren, wobei das Hauptinteresse in der porenbildenden Membranfraktion lag. Durch Zentrifugation über einen diskontinuierlichen Zuckergradienten konnten die Membranvesikel in zwei verschiedene Vesikelfraktionen aufgetrennt werden. Eine Membranfraktion konnte aus der 40%igen Zuckerfraktion („40% Membranfraktion“) isoliert werden, die andere aus der 30%igen Zuckerfraktion („30% Membranfraktion“). Die verschiedenen Membranfraktionen wurden zu in vitro Kernen gegeben, in denen die Kernporen durch vorausgegangene Bildung von Annulate Lamellae depletiert worden waren. Nach Zugabe der 30% Membranfraktion konnte die Bildung von funktionalen Kernporen beobachtet werden. Im Gegensatz dazu zeigte die 40% Membranfraktion keine porenbildenden Eigenschaften. Unter Verwendung eines vereinfachten Systems, bestehend aus Zytosol, Spermienchromatin und den Membranen, wurde gezeigt, dass die 40% Membranfraktion an Chromatin bindet und ausreichend ist, um eine kontinuierliche Doppelmembran ohne Kernporen zu bilden. Die 30% Membranfraktion besitzt keine Chromatinbindungseigenschaften und wird aktiv entlang von Mikrotubuli zu den porenlosen Kernen transportiert. Dort interagiert sie mit der chromatingebundenen 40% Membranfraktion und induziert die Porenbildung. Nach dem Vergleich der Proteinzusammensetzung der beiden Membranfraktionen, konnte das Major Vault Protein (MVP) nur in der porenbildenden Membranfraktion gefunden werden. MVP ist die Hauptstrukturkomponente der Vault-Komplexe, einem Ribonukleo-proteinpartikel, der in den meisten eukaryotischen Zellen vorhanden ist (Kedersha et al., 1991). Bemerkenswerterweise wird über die Funktion der Vault-Komplexe, trotz ihrer übiquitären Expression und ihrem Vorkommen in fast allen eukaryotischen Zellen, immer noch diskutiert. Um mehr über die Funktion und die Lokalisation der Vaults/MVP zu lernen, wurden die Vaults in Anlehnung an die Methode von Kedersha und Rome (1986) aus Xenopus Eiern isoliert. Zusätzlich wurde rekombinantes Xenopus MVP hergestellt, das unter anderem für die Produktion von Antikörpern in Meerschweinchen verwendet wurde. Um herauszufinden, ob die Anwesenheit von MVP in der 30% Membranfraktion in direktem Zusammenhang mit deren porenbildender Eigenschaft steht, wurden gereinigte Vault-Komplexe oder rekombinantes MVP, das alleine ausreichend ist, um in sich zu den charakteristischen Vault-Strukturen zusammenzulagern, zu porenlosen Kernen gegeben. Sowohl gereinigte Vault-Komplexe, als auch rekombinantes MVP waren in der Lage in den porenlosen Kernen die Bildung von funktionalen Kernporen zu induzieren. Untersuchungen zur Lokalisation von MVP zeigten, dass MVP teilweise an der Kernhülle und den Kernporenkomplexen lokalisiert, während der Großteil an MVP zytoplasmatisch vorliegt. Dies sind die ersten Daten, die Vaults/MVP mit der Kernporenbildung in Verbindung bringen. Deshalb bietet diese Arbeit die Grundlage, um diese unerwartete Rolle der Vaults in Zukunft genauer zu charakterisieren. / The nuclear envelope (NE) is a highly specialized membrane that delineates the eukaryotic cell nucleus. It is composed of the inner and outer nuclear membranes that are connected by the nuclear pore complexes (NPCs). The NE not only regulates the trafficking of macromolecules between nucleoplasm and cytosol but also provides anchoring sites for chromatin and cytoskeleton. Through these interactions, the NE helps position the nucleus within the cell and chromosomes within the nucleus, thereby regulating the expression of certain genes. In higher eukaryotic cells, both NE and NPCs undergo structural changes during cell division as they disassemble at the onset of mitosis and need to reform in the daughter cells at the end of mitosis. The molecular mechanisms governing the reassembly of the NE are only poorly understood. A particular suitable system to analyze specific events involved in NE assembly is provided by the cell-free system based on Xenopus egg extract and sperm chromatin (Lohka 1998). Previously it could be shown that in Xenopus egg extract there exist at least two different vesicle populations that are involved in nuclear envelope assembly. One type of vesicle binds to chromatin where it fuses and forms a bilayered nuclear envelope. The other vesicle population binds to the double nuclear membrane and is required for nuclear pore complex formation. Aim of this study was to isolate and characterize these two membrane fractions with special regard to the pore-forming membrane fraction. By centrifugation on a discontinuous sucrose gradient the membrane vesicles could be separated into two different vesicle fractions. One membrane fraction was recovered from the 40% sucrose fraction (“40% membrane fraction”) and the other one from the 30% sucrose fraction (“30% membrane fraction”). The different membrane fractions were added to in vitro nuclei, where nuclear pores were depleted by formation of annulate lamellae. After addition of the 30% membrane fraction formation of functional nuclear pores could be observed. In contrast the 40% membrane fraction had no pore-forming property. Using a simplified system consisting of cytosol, spermchromatin an membranes it was demonstrated that the 40% membrane fraction binds to chromatin and is sufficient to form a continuous double membrane without NPCs. The 30% membrane fraction lacks chromatin targeting signals and is actively transported along microtubules to the pore-free nuclei. There it interacts with the chromatin-bound 40% membranes and induces formation of NPCs. Comparing the protein composition of both membrane fractions, the major vault protein (MVP) was found to be exclusively in the pore-inducing membrane fraction. MVP is the major structural component of vaults, a ribonucleoprotein particle found in most eukaryotic cells (Kedersha et al., 1991). Remarkably, despite their ubiquitous expression and abundance in nearly all eukaryotic cells, the functional role of vaults is still being debated. To learn more about the functional role and localization of vaults/MVP, vaults were isolated from Xenopus eggs following the procedure of Kedersha and Rome (1986). In addition recombinant Xenopus MVP was prepared and used to generate antibodies in guinea pigs. To find out whether the presence of MVP in the 30% membrane fraction is related to its pore-forming capacity, purified vault complexes or recombinant MVP, which alone is sufficient to selfassemble into the characteristic vault structure, were added to poreless nuclei. Both purified vaults and recombinant MVP induce the formation of functional NPCs in the pore-free nuclei. Studying the localization of MVP it was demonstrated, that MVP localizes in part at the nuclear envelope and the nuclear pore complexes, whereas most MVP is cytoplasmically. These are the first data that link vaults/MVP to NPC assembly. Therefore this work displays fundamental features to study this unexpected role of vaults in more detail.
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Modulação da expressão dos genes para melanopsina, clock, per1, per2 e bmal1 por melatonina em melanóforos dérmicos do anfíbio Xenopus laevis / Modulation of the expression of melanopsin, clock, per1, per2 e bmal1 , and by melatonin in dermal melanophores of Xenopus laevisBluhm, Ana Paula Canel 11 July 2008 (has links)
O ritmo diário de atividade é uma característica de todos os organismos vivos, que tem a capacidade de se orientar no tempo e no espaço, e distinguir entre tempo linear e tempo cíclico. O ciclo claro:escuro é um importante indicador circadiano para todos os organismos. O trabalho do relógio circadiano envolve mecanismos de retroalimentação positiva e negativa dos genes CLOCK e BMAL1 (brain and muscle Arnt-like protein 1) que formam um heterodímero, funcionando como fator de transcrição para a expressão dos genes per (period), cry (cryptochrome) e o receptor órfão REV-ERB. Em geral, o ciclo circadiano tem início nas primeiras horas da manhã com a ativação da transcrição de per e cry por CLOCK/BMAL1. A periodicidade do relógio circadiano resulta da combinação entre retroalimentação transcricional positiva e negativa destes genes. Hoje já se sabe que os vertebrados, além do relógio central (NSQ) possuem vários relógios, distribuídos pelo corpo, os chamados relógios periféricos. A resposta ao estímulo luminoso é resultado da interpretação da informação luminosa por diferentes tipos celulares. A molécula fotorreceptora de melanóforos dérmicos embrionários de X. laevis foi denominada melanopsina (Opn4/Opn4). Neste anfíbio, cones e bastonetes, continuam a exibir ritmo circadiano em cultura durante vários dias, e a sua capacidade de se ajustar pelo estímulo luminoso indica a presença do sistema circadiano. Os objetivos deste projeto foram: verificar qual é o padrão de expressão para Opn4, per1, per2, bmal1 e clock em melanóforos de X. laevis submetidos a diferentes fotofases; verificar se a expressão para Opn4, per1, per2 ,bmal1 e clock nos melanóforos de X. laevis é modulada pela melatonina. Opn4, per1, per2 ,bmal1 e clock Dados obtidos no presente estudo demonstram que nesta linhagem celular estes genes apresentam um padrão de expressão aparentemente rítmico, quando estas células são expostas a um ciclo claro:escuro (14C:10E), que difere do padrão obtido quando mantidas em regime de escuro constante. Em geral, estas células mantidas em escuro constante durante 5 dias tendem a apresentar aumento de expressão de RNAm para estes genes e, quando mantidas em escuro constante também durante 5 dias, mas com adição de melatonina por 1h, 24 h antes de sua extração, estes níveis de RNAm tendem a diminuir. Porém, quando comparamos as três situações, podemos observar que a adição da melatonina restaura, em geral, o padrão de expressão dos genes analisados em 14C:10E. O conjunto de resultados, que obtivemos em melanóforos dérmicos de Xenopus laevis, sugere que esta linhagem celular possue características de relógio periférico. / The daily rhythm of activity is a characteristic of all living organisms, which have the ability of to behave accordingly time and space, and distinguish between linear and cyclic time. The dark:light cycle is an important time cue for all organisms. The work of circadian clock involves mechanisms of positive and negative feedback of CLOCK and BMAL1 which as a heterodimer act as a transcription factor for the expression of per (period), cry (cryptochrome) and the orphan receptor REV-ERB. A typical circadian cycle begins in the first hours of daytime, which the activation of the transcription of per and cry by CLOCK/BMAL1. It is well known that the vertebrates, besides the central clock (SCN), have several other clocks distributed by the body, the so called peripheric clock. The responses to light are the result of the interpretation of light signal by several cell types The photoreceptor molecule in the dermal melanophores of X. laevis was denominated melanopsin (Opn4/Opn4). In this amphibian, rods and cones maintain circadian rhythm during several days in culture, and their ability to synchronize by light suggest the presence of a circadian system. The objectives of this project were: verify the expression pattern for Opn4, per1, per2 ,bmal1 e clock in dermal melanophores of X. laevis, under different photo phases; and verify whether the expression for Opn4, per1, per2, bmal1 and clock were modulated by melatonin. Our data show that these genes have a rhythmic pattern expression, when these cells are under a 14L:10D, which is different from the pattern exhibited in constant dark. In general, these cells in constant dark have a higher mRNA expression, and in the same condition, but with melatonin applied for 1h, 24h before the data collect, these mRNA levels are lower. However, when we compared these three different experimental conditions, we observed that melatonin resets, in overall, the expression pattern of 14L:10D. These data, taken together, suggest that Xenous laevis dermal melanophores have characteristics of a peripheric clock.
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Evolution of Xenopus Vocal Patterns: Retuning a Hindbrain Circuit During Species DivergenceBarkan, Charlotte Barkan January 2017 (has links)
Circuits underlying motor patterns of closely related species provide an ideal framework in which to study how evolution shapes behavioral variation. Male African clawed frogs (Xenopus and Silurana) advertisement call to attract female mates and silence male rivals. Males of each species produce a unique vocal pattern that serves as a species-identifier. Xenopus laevis is the most well-studied species in terms of its vocal behavior and underlying anatomy and physiology. The clade that includes X. laevis, or X. laevis senso lato, also includes 3 other species that diverged ~8.5 million years ago. All 4 of these species produce advertisement calls that include fast trills – trains of fast rate (~60 Hz) sound pulses. However, their calls differ substantially between species in measures of trill duration and period. I examined the premotor circuit underlying vocal patterning in three of these species: X. laevis, X. petersii, and X. victorianus. I used extracellular recordings to find that a premotor nucleus, DTAM, which is part of the vocal central pattern generator, is the likely source of species-variation of vocal patterns. Species-specific trill duration and period are intrinsic to the region of the hindbrain that includes DTAM. Next, I used blind whole-cell patch recordings in DTAM of X. laevis and X. petersii to examine the cells that encode trill duration and period. I identified homologous populations of premotor vocal cells in both species that code for trill duration and period in a species-specific manner. Together, these results support an autonomous role of the DTAM circuit for generation of species variation in call duration and period.
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USING THE FROG EPIDERMIS TO UNCOVER DESMOSOME FUNCTION AND REGULATION IN THE DEVELOPING EMBRYOBharathan, Navaneetha Krishnan 01 January 2018 (has links)
The desmosome is one of the major cell adhesion junctions found in the epithelia, heart, and hair follicle. Described as a “rivet” that hold cells together, it provides these tissues with the integrity to withstand the tremendous forces they face in everyday life. Defects in this junction can lead to devastating diseases where patients are susceptible to skin infections and cardiovascular defects. Limited treatments exist for diseases of the desmosome, and strategies do not target all symptoms. Therefore, delineating the function and regulation of desmosomes is of paramount importance for the development of prevention and treatment strategies. The Xenopus laevis has been utilized for the study of embryonic development and tissue movements. This study takes advantage of the frog model to study a key desmosomal protein, desmoplakin (Dsp), in the epidermal development of the embryo. First, Xenopus embryonic epidermis has junctional desmosomes as early as the blastula stages. Desmosomes numbers per junction increase as the embryo develops. Dsp is present in many epidermally-derived structures in the embryo at varying levels. Xenopus embryos deficient in desmoplakin have phenotypic defects in epidermal structures and the heart, mimicking mammalian models. Embryos with reduced Dsp exhibit an increased susceptibility to epidermal damage under applied mechanical forces. Assays also reveal a potential role for desmosomes in radial intercalation, a process through which cells move from the inner to the outer epidermal layers. Embryos with reduced Dsp exhibit a slight reduction in intercalation and defects in intercalating cell types, including multiciliated cells and small secretory cells. Finally, c-Jun N-terminal kinase (JNK) may have a potential role in the regulation of desmosome assembly and adhesion. Embryos with deficient Dsp display a partial recovery of mechanical integrity when treated with a JNK inhibitor.
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Methods to Characterize Orofacial DevelopmentCherry, Amanda M 01 January 2018 (has links)
In this thesis, several techniques were combined to optimize, evaluate and characterize craniofacial development in Xenopus, with additional focus on understanding the alterations made during maturation in the craniofacial region and the cartilage. Three important techniques used were: confocal microscopy in conjunction with Acridine Orange (AO) labeling, Alcian Blue (AB) labeling, and geometric morphometric analysis. I found that facial width increased across all techniques used to evaluate it. Included within this focus was the study of the development of the ceratohyal (CH) cartilage, which supported the mouth and snout. This was also found to increase width wise, in unison with facial and orofacial growth. This data may suggest a link between the face, mouth and CH growth, in which the developing cartilage elongates and widens causing the increase seen in the width and distension of the mouth.
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