The deposition of superconducting Nb3 Sn on copper accelerating cavities is interesting for the higher thermal conductivity of copper compared to common Nb substrates. The better heat exchange would allow the use of cryocoolers reducing cryogenic costs and the risk of thermal quench [1]. The magnetron sputtering technology allows the deposition of Nb 3 Sn on substrates different than Nb, however the coating of substrates with complex geometry (such as elliptical cavities) may require target with non-planar shape, which are difficult to realize with classic powder sintering techniques. In this work, the possibility of using the Liquid Tin Diffusion (LTD) technique to produce sputtering targets is explored. The LTD technique is a wire fabrication technology, already developed in the past at LNL for superconducting radio frequency (SRF) applications [2], that allows the deposition of very thick and uniform coating on Nb substrates even with complex geometries [3]. Improvements in LTD process, proof of concept of a single use LTD target production, and characterization of the Nb 3 Sn film coated by DC magnetron sputtering with these innovative targets are reported in this work.

Over the last decade, the interstitial alloying of niobium has proven to be essential for enabling superconducting radiofrequency (SRF) cavities to operate more efficiently at high accelerating gradients. The discovery of "nitrogen doping" was the first readily accessible avenue of interstitial alloying in which researchers saw an increase in cavity performance. However, the serendipitous nature of the discovery led to additional research to fundamentally understand the physics behind the increase in cavity performance. This knowledge gap is bridged by materials characterization. Secondary ion mass spectrometry (SIMS) is a characterization technique which has become a staple of SRF cavity characterization that details elemental concentration profiles as a function of depth into the niobium surface with submicron resolution. SIMS has been widely used by the semiconductor industry for decades but has found less application in other fields due to the difficulty to produce reproducible data for polycrystalline materials. Much effort has been given to reduce the uncertainty of SIMS results to as low as 1% - 2% for single crystals. However, less attention has been given to polycrystalline materials with uncertainty values reported between 40% - 50% The sources of uncertainty were found to be deterministic in nature and therefore could be mitigated to produce reliable results. This dissertation documents the efforts to reduce SIMS method uncertainty which has been further used to solve mysteries regarding the characterization of SRF cavities which include predictive modeling of oxygen diffusion as well as the identification of contaminants resulting from cavity furnace treatments. / Doctor of Philosophy / Particle accelerators find many uses in society in which their complexity depends on their intended purpose. These purposes vary from projecting an image as in cathode ray tube (CRT) TVs, to creating high energy x-rays for life saving cancer treatments, to researching the very fundamental principles of science and physics. The later uses particle accelerators which are very large, spanning multiple miles, and run at extremely high energies. To keep operational costs reasonable, these instruments need to run as efficiently as possible. Therefore, superconducting radiofrequency (SRF) niobium cavities are used and are responsible for propulsion of charged particles. Although, niobium SRF cavities can pass incredibly high currents with very little surface resistance, these high-end particle accelerators push the operational boundaries of efficiency. To improve the efficiency of these cavities, an optimal concentration of impurities, such as oxygen and nitrogen, are added to the niobium surface. The addition of an impurity level that is too high or too low causes the resistance to increase which translates to higher operational costs. Therefore, it is important to accurately determine the concentration of impurities within the niobium and with high depth resolution. Secondary ion mass spectrometry is a characterization method that uses a primary ion beam to impact the surface of a material to remove atoms at the very surface. The ejected atoms are then ionized into a secondary beam which can then be detected to determine the concentration and to identify the species which was removed. Historically, this instrument has yielded results with 40% - 50% uncertainty for polycrystalline metals, such as niobium, which do not sputter evenly. With SRF cavity performance depending on accurate quantitation of impurities, a more robust method is needed. Therefore, this dissertation identifies issues which cause high uncertainties for polycrystalline materials and in addition offers mitigation strategies to reduce uncertainty to below 10%. These methods were then applied to solve real problems aimed to improve the production of niobium SRF cavities.

Im Zuge der frühen embryonalen Herzentwicklung entstehen ausgehend von einem einfachen Herzschlauch zwei deutlich voneinander getrennte Herzkammern. Die Kardiomyozyten des Atriums und Ventrikels weisen spezifische Eigenschaften auf, die sich morphologisch wie auch funktionell auf das Herz auswirken. Veränderungen in der Gewebsarchitektur werden hauptsächlich durch Zellinterkalation und kollektive Zellmigration erreicht. Viele Studien zeigen, dass der Wnt/PCP-Signalweg eine essentielle Rolle in der Regulation dieser Bewegungen einnimmt. Die Daten dieser Studie belegen, dass die nicht-kanonischen Liganden Wnt11 und Wnt5b sowie die Kernkomponenten des PCP Signalweges Fzd7, Vangl2, Dvl2 und Pk1 an der Steuerung der Reorganisation der Kardiomyozyten während der Kammerbildung beteiligt sind, was Einfluss auf die Architektur des frühen Myokardiums nimmt. Effektoren des PCP Signalweges umfassen das Zytoskelett sowie Adhäsions- und Migrationsprozesse. In dieser Studie wird gezeigt, dass die Komponenten dieses Signalweges im Myokardium hauptsächlich Prozesse der Actomyosin Modulation regulieren und damit unter anderem die Morphologie der Kardiomyozyten beeinflussen. Zusätzlich ist die frühe Kardiogenese durch eine Relokalisierung der phosphorylierten Form der Myosin Regulatory Light Chain (MRLC) vom Kern zur Membran gekennzeichnet. Hier wird gezeigt, dass die Phosphorylierung von MRLC sowie die Relokalisation von den Kernkomponenten des PCP Signalweges kontrolliert werden sowie dass es im Verlauf der frühen Herzentwicklung u.a. durch die Relokalisierung von pMRLC zu Änderungen in der Gewebespannung kommt, welche sich auf die nukleäre Spannung auswirken und damit Veränderungen in der Genregulation hervorrufen. Diese Veränderungen werden hauptsächlich durch Effekte auf die Lokalisation und Aktivität des Serum Response Factors (SRF) vermittelt, welche in diesem Kontext durch die PCP Kernkomponente Pk1 reguliert sind. / Formation of a complex multiple-chambered heart from the simple linear heart tube does not only require orchestrated morphogenesis of the myocardium, but also cardiac muscle differentiation and changes in intercellular electrical coupling. To date, the processes that lead to the formation of a functional syncytium are incompletely understood. One of the major pathways controlling multiple aspects of organogenesis and tissue morphogenesis is the planar cell polarity (PCP) pathway. Changes in tissue architecture are controlled by cell intercalation and collective cell migration. It is widely accepted that Wnt/PCP signaling plays a crucial role in guiding these cellular processes. This study provides evidence that morphogenesis of the heart is controlled by the non-canonical ligands Wnt11 and Wnt5b and the PCP core components Fzd7, Vangl2, Dvl2, and Pk1 through regulation of cell rearrangements during embryonic cardiac remodeling. Downstream effectors of the PCP pathway target adhesion processes, cytoskeleton, and migration. Here, it is revealed that PCP signaling in the heart affects cardiomyocyte morphology and actomyosin organization. Specifically, changes in the subcellular localization of the phosphorylated non-muscle myosin II regulatory light chain (pMRLC) at LHT stage are targeted by the PCP pathway core components. Furthermore, actomyosin relocalization concurs with changes in nuclear tension and SRF signal transduction within the myocardium. This study unravels a novel function of the PCP core component Pk1 in regulation of SRF translocation and target gene expression that is critical to cardiac maturation. Taken together, this study provides evidence that the PCP pathway is a major regulator of cardiac remodeling and organ maturation by modulating mechanosensitive SRF signal transduction involved in muscle differentiation.

The transverse emittance is one of the most important quantities which characterize the quality of an electron source. For high quality experiments low beam emittance is required. By means of theoretical considerations and simulation calculations we have studied how the emittance of the Rossendorf superconducting radio-frequency photoelectron source (SRF gun) can be minimized. It turned out that neither a solenoid magnet nor the effect of space charge forces is needed to create a pronounced emittance minimum. The minimum appears by just adjusting the starting phase of the electron bunch with respect to the RF phase of the gun in a suitable way. Investigation of various correlations between the properties of the beam particles led to an explanation on how the minimum comes about. It is shown that the basic mechanism of minimization is the fact that the longitudinal properties of the particles (energy) are strongly influenced by the starting phase. Due to the coupling of the longitudinal and transverse degrees of freedom by the relativistic equation of motion the transverse degrees of freedom and thereby the emittance can be strongly influenced by the starting phase as well. The results obtained in this study will be applied to minimize the emittance in the commissioning phase of the SRF gun.

Le muscle squelettique adulte est un tissu possédant la capacité fondamentale d’adapter sa taille à la demande fonctionnelle : il peut s’atrophier ou s’hypertrophier en réponse à une variation de la charge mécanique qui lui est appliquée. A l’heure actuelle, les facteurs impliqués dans la plasticité musculaire demeurent méconnus. D’une part, grâce à différents modèles d’atrophie musculaire, nous démontrons que le facteur de transcription Srf joue le rôle de médiateur de la mécano-transduction par la voie actine/Mrtfs/Srf. L’arrêt de l’activité mécanique provoque une accumulation nucléaire d’actine monomérique, une délocalisation de Mrtf-A, coactivateur de Srf, et une diminution de l’activité de Srf, se traduisant notamment par une baisse de la transcription Srf-dépendante. Les gènes cibles de Srf comptant un grand nombre de protéines sarcomériques, telles que l’α-actine squelettique, la réduction de leur expression pourrait participer à l’atrophie musculaire. De plus, nos travaux suggèrent que la diminution de l’activité de Srf pourrait influencer l’organisation du réseau mitochondrial et le flux autophagique par des mécanismes qui restent à élucider. D’autre part, en tirant parti d’un modèle d’invalidation conditionnelle et inductible de Srf dans les cellules satellites, nous montrons que le phénomène d’hypertrophie compensatoire requiert l’expression de Srf par les cellules satellites. L’absence de Srf n’altère ni la prolifération ni l’entrée en différenciation des myoblastes, néanmoins elle provoque un défaut de fusion des myoblastes aux fibres au cours de l’hypertrophie induite par surcharge. Ainsi, nos travaux démontrent que Srf est un acteur majeur de la plasticité musculaire, à la fois en tant que médiateur de la mécano-transduction par la voie actine/Mrtfs/Srf et par son implication dans la fusion des cellules satellites aux fibres musculaires, nécessaire à l’hypertrophie compensatoire. / Adult skeletal muscle is able to adapt its size to functional demand. It can undergo atrophy or hypertrophy according to mechanical load. To date, the molecules that mediate muscle plasticity remain unclear.Using different models inducing muscle atrophy, we show that the transcription factor Srf is a mediator of mechanotransduction through the actin/Mrtfs/Srf pathway. Mechanical load abolition leads to G-actin nuclear accumulation, delocalization of Mrtf-A, an Srf coactivator, and Srf activity downregulation. This results in a decrease in Srf-dependent transcription. Many Srf target genes encode sarcomeric proteins such as α-skeletal actin, thus a downregulation of Srf-dependent transcription could participate to muscle atrophy. In addition, our results suggest that Srf activity decrease could affect mitochondrial network organization and autophagic flux in a way that remains to be determined. Besides, using a satellite cell-specific conditional and inducible Srf knockout, we show that overload hypertrophy requires Srf expression by satellite cells. Myoblasts proliferation and early differentiation are not altered by Srf loss. However, mutant myoblasts are unable to fuse with myofibers during overload hypertrophy. Altogether, our results demonstrate that Srf is an important player in skeletal muscle plasticity: it is a mediator of mechanotransduction via the actin/Mrtfs/Srf pathway and its expression by satellite cells is required for myoblasts to fuse with myofibers during overload hypertrophy.

The advantages of contemporary particle injectors are high bunch charges and good beam quality in the case of normal conducting RF guns and increased repetition rates in the one of DC injectors. The technological edge of the concept of superconducting radio frequency injectors is to combine the strengths of both these sides. As many future accelerator concepts, such as energy recovery linacs, high power free electron lasers and certain collider designs, demand particle sources with high bunch charges and high repetition rates combined, applying the superconductivity of the accelerator modules to the injector itself is the next logical step. However, emittance compensation — the cornerstone for high beam quality — in case of a superconducting injector is much more challenging than in the normal conducting one. The use of simple electromagnets generating a solenoid field around the gun’s resonator interferes with its superconducting state. Hence, it requires novel and sophisticated techniques to maintain the high energy gain inside the gun cavity, while at the same time alleviating the detrimental fast transverse emittance growth of the bunch. In the case of the ELBE accelerator at the Helmholtz-Zentrum Dresden-Rossendorf, a superconducting electron accelerator provides beam for several independent beamlines in continuous wave mode. The applications include IR to THz free electron lasers, neutron and positron generation, to Thompson backscattering with an inhouse TW laser, and hence, call for a flexible CW injector. Therefore, the development of a 3.5 cell superconducting electron gun was initiated in 1997. The focus of this thesis lies on three approaches of transverse emittance compensation for this photoinjector: RF focusing, the installation of a superconducting solenoid close to the cavity’s exit, and the introduction of a transverse electrical mode of the RF field in the resonator. All three methods are described in theory, examined by numerical simulation, and experimentally reviewed in the particular case of the ELBE SRF Gun II at HZDR and a copy of its niobium resonator at Thomas Jefferson National Laboratory, Newport News, VA, USA.

The advantages of contemporary particle injectors are high bunch charges and good beam quality in the case of normal conducting RF guns and increased repetition rates in the one of DC injectors. The technological edge of the concept of superconducting radio frequency injectors is to combine the strengths of both these sides. As many future accelerator concepts, such as energy recovery linacs, high power free electron lasers and certain collider designs, demand particle sources with high bunch charges and high repetition rates combined, applying the superconductivity of the accelerator modules to the injector itself is the next logical step. However, emittance compensation — the cornerstone for high beam quality — in case of a superconducting injector is much more challenging than in the normal conducting one. The use of simple electromagnets generating a solenoid field around the gun’s resonator interferes with its superconducting state. Hence, it requires novel and sophisticated techniques to maintain the high energy gain inside the gun cavity, while at the same time alleviating the detrimental fast transverse emittance growth of the bunch. In the case of the ELBE accelerator at the Helmholtz-Zentrum Dresden-Rossendorf, a superconducting electron accelerator provides beam for several independent beamlines in continuous wave mode. The applications include IR to THz free electron lasers, neutron and positron generation, to Thompson backscattering with an inhouse TW laser, and hence, call for a flexible CW injector. Therefore, the development of a 3.5 cell superconducting electron gun was initiated in 1997. The focus of this thesis lies on three approaches of transverse emittance compensation for this photoinjector: RF focusing, the installation of a superconducting solenoid close to the cavity’s exit, and the introduction of a transverse electrical mode of the RF field in the resonator. All three methods are described in theory, examined by numerical simulation, and experimentally reviewed in the particular case of the ELBE SRF Gun II at HZDR and a copy of its niobium resonator at Thomas Jefferson National Laboratory, Newport News, VA, USA.

La réduction du cout de construction et d’exploitation des futurs accélérateurs d particules, a grande et petite échelles, dépend du développement de nouveaux matériaux pour les surfaces actives des structures supraconductrices en radiofréquence (SRF). Les propriétés SRF sont essentiellement un phénomène de surface vu que la profondeur de pénétration (profondeur de pénétration de London, λ) des micro-ondes (RF) est typiquement de l’ordre de 20 à 400 nm en fonction du matériau. Lorsque les procédés de préparation de surface sont optimises, la limite fondamentale du champ RF que les surfaces SRF peuvent supporter est le champ RF maximum, Hc₁, au-delà duquel le flux magnétique commence à pénétrer la surface du supraconducteur. Le matériau le plus utilise pour des applications SRF est le niobium (Nb) massif, avec un champ Hc₁ de l’ordre de 170 mT, qui permet d’atteindre un champ accélérateur de moins de 50 MV/m. Les meilleures perspectives d’amélioration des performances des cavités SRF sont liées à des matériaux et méthodes de production produisant la surface SRF critique de façon contrôlée. Dans cette optique, deux avenues sont explorées pour utiliser des couches minces pour augmenter les performances des structures SRF au-delà du Nb massif, en monocouche ou en structures multicouches Supraconducteur-Isolant-Supraconducteur (SIS) : La première approche est d’utiliser une couche de Nb déposée sur du cuivre (Nb/Cu) à la place du Nb massif. La technologie Nb/Cu a démontré, au cours des années, être une alternative viable pour les cavités SRF. Toutefois, les techniques de dépôt communément utilisées, principalement la pulvérisation magnétron, n’ont jusqu’à présent pas permis de produire des surfaces SRF adaptées aux performances requises. Le récent développement de techniques de dépôt par condensation énergétiques, produisant des flux d’ions énergétiques de façon contrôlée (telles que des sources d’ions ECR sous ultravide) ouvrent la voie au développement de films SRF de grand qualité. La corrélation entre les conditions de croissance, l’énergie des ions incidents, la structure et les performances RF des films produits est étudiée. Des films Nb avec des propriétés proches du Nb massif sont ainsi produits. La deuxième approche est basée sur un concept qui propose qu’une structure multicouche SIS déposée sur une surface de Nb peut atteindre des performances supérieures à celles du Nb massif. Bien que les matériaux supraconducteurs à haute Tc aient un champ Hc₁ inférieur à celui du Nb, des couches minces de tels matériaux d’une épaisseur (d) inférieure à la profondeur de pénétration voient une augmentation de leur champ parallèle Hc₁ résultant au retardement de la pénétration du flux magnétique. Cette surcouche peut ainsi permettre l’écrantage magnétique de la surface de Nb qui est donc maintenue dans l’état de Meissner à des champs RF bien plus importants que pour le Nb massif. La croissance et performance de structures multicouches SIS basées sur des films de NbTiN, pour le supraconducteur, et de l’AlN, pour le diélectrique, sont étudiées. Les résultats de cette étude montrent la faisabilité de cette approche et le potentiel qui en découle pour l’amélioration des performances SRF au-delà du Nb massif. / The minimization of cost and energy consumption of future particle accelerators, both large and small, depends upon the development of new materials for the active surfaces of superconducting RF (SRF) accelerating structures. SRF properties are inherently a surface phenomenon as the RF only penetrates the London penetration depth λ, typically between 20 and 400 nm depending on the material. When other technological processes are optimized, the fundamental limit to the maximum supportable RF field amplitude is understood to be the field at which the magnetic flux first penetrates into the surface, Hc₁. Niobium, the material most exploited for SRF accelerator applications, has Hc₁~170 mT, which yields a maximum accelerating gradient of less than 50 MV/m. The greatest potential for dramatic new performance capabilities lies with methods and materials which deliberately produce the sub-micron-thick critical surface layer in a controlled way. In this context, two avenues are pursued for the use of SRF thin films as single layer superconductor or multilayer Superconductor-Insulator-Superconductor structures: Niobium on copper (Nb/Cu) technology for superconducting cavities has proven over the years to be a viable alternative to bulk niobium. However the deposition techniques used for cavities, mainly magnetron sputtering, have not yielded, so far, SRF surfaces suitable for high field performance. High quality films can be grown using methods of energetic condensation, such as Electron Cyclotron Resonance (ECR) Nb ion source in UHV which produce higher flux of ions with controllable incident angle and kinetic energy. The relationship between growth conditions, film microstructure and RF performance is studied. Nb films with unprecedented “bulk-like” properties are produced. The second approach is based on the proposition that a Superconductor/Insulator/Superconductor (S-I-S) multilayer film structure deposited on an Nb surface can achieve performance in excess of that of bulk Nb. Although, many higher-Tc superconducting compounds have Hc₁ lower than niobium, thin films of such compounds with a thickness (d) less than the penetration depth can exhibit an increase of the parallel Hc₁ thus delaying vortex entry. This overlayer provides magnetic screening of the underlying Nb which can then remain in the Meissner state at fields much higher than in bulk Nb. A proof of concept is developed based on NbTiN and AlN thin films. The growth of NbTiN and AlN films is studied and NbTiN-based multilayer structures deposited on Nb surfaces are characterized. The results from this work provide insight for the pursuit of major reductions in both capital and operating costs associated with future particle accelerators across the spectrum from low footprint compact machines to energy frontier facilities.

Ο έλεγχος της έκφρασης των πρωτεϊνών που χαρακτηρίζουν τον Λείο Μυικό Φαινότυπο (ΛΜΦ) είναι εξαιρετικής σημασίας για την κατανόηση, σε μοριακό επίπεδο, διεργασιών που σχετίζονται με πολλές φυσιο-παθολογικές καταστάσεις στον άνθρωπο. Μεταξύ των ασθενειών όπου ο ΛΜΦ είναι καθοριστικής σημασίας για την ανάπτυξη και εξέλιξή τους, είναι η αθηροσκλήρωση, η υπέρταση, η επαναστένωση των αρτηριών μετά από αγγειοπλαστική, η ίνωση οργάνων όπως οι πνεύμονες, το ήπαρ και οι νεφροί, και η ανάπτυξη μεταστάσεων από συμπαγείς όγκους. Επομένως, κατανόηση των κυτταρικών και μοριακών μηχανισμών που οδηγούν σε τροποποίηση του ΛΜΦ είναι βασικής σημασίας για την αναγνώριση στρατηγικών περιορισμού της εξέλιξης των νόσων αυτών και της εκδήλωσης των κλινικών συνεπειών τους. Αρχικό στόχο αποτέλεσε η ανάπτυξη και καθιέρωση ενός in vitro προτύπου συστήματος για την διαφοροποίηση μη διαφοροποιημένων κυττάρων προς φαινότυπο που προσομοιάζει με αυτό των Λείων Μυικών Κυττάρων (ΛΜΚ), ώστε να χρησιμεύσει στη μελέτη του μοριακού καθορισμού και ελέγχου του φαινότυπου των κυττάρων αυτών. Πρώτα-πρώτα, χαρακτηρίσαμε βασικά, σημαντικά «μοριακά εργαλεία» για την διαπίστωση και μοριακή διερεύνηση του ΛΜ-φαινοτύπου. Χρησιμοποιώντας τα, αναπτύξαμε και χαρακτηρίσαμε πρωτογενώς ένα πρότυπο σύστημα διαφοροποίησης σε ΛΜΚ, βασιζόμενο σε Μεσεγχυματικά Βλαστικά Κύτταρα (ΜΒΚ) προερχόμενα από γέλη Wharton ομφάλιου λώρου. Στα κύτταρα αυτά, η έκφραση γονιδίων και πρωτεϊνών που χαρακτηρίζουν τον ΛΜΦ εξαρτάται από την επαρκή έκφραση της πρωτεΐνης Serum Response Factor (SRF), από την ύπαρξη αλληλουχιών Serum Response Element (SRE) στον υποκινητή των εξεταζόμενων ΛΜΚ-ειδικών γονιδίων, και επάγεται από εξωγενή έκφραση της Μυοκαρδίνης. Επομένως, όπως έχει περιγραφεί και για άλλα πρότυπα συστήματα, η διαφοροποίηση των κυττάρων αυτών σε κύτταρα που προσομοιάζουν ΛΜΚ στηρίζεται στην συνέργεια δύο μεταγραφικών παραγόντων, του SRF και της Μυοκαρδίνης. Το πρότυπο αυτό θα είναι χρήσιμο για να διερευνήσουμε τους μοριακούς μηχανισμούς δράσης φυσιολογικών και φαρμακολογικών παραγόντων στον έλεγχο του ΛΜΦ. Επί πλέον, το πρότυπο σύστημα αυτό δύναται να αποβεί χρήσιμο για την κατανόηση εν γένει διεργασιών που οδηγούν στην βασική κυτταρική αλλαγή γνωστή ως Επιθηλιακή-Μεσεγχυματική Μετάβαση (ΕΜΤ) και κατ’ επέκταση για την κατανόηση μηχανισμών παθογένειας πλείστων νόσων που χαρακτηρίζονται από ΕΜΤ. Παράλληλα, έγινε προσπάθεια διερεύνησης αν η κυτταρική σειρά A7r5 αγγειακών ΛΜΚ αποτελεί βιώσιμο φαρμακολογικό σύστημα για την διερεύνηση των μηχανισμών μέσω των οποίων η έκφραση του ΛΜΦ ελέγχεται σε μοριακό επίπεδο από τους αδρενεργικούς υποδοχείς, μία οικογένεια υποδοχέων που διαδραματίζουν σημαντικό ρόλο στην ομοιόσταση του αγγειακού τοιχώματος και στην αρτηριακή παθοφυσιολογία. Δείξαμε ότι ο κυτταρικός πληθυσμός A7r5 δεν απαντά σε α1-αδρενεργική διέγερση διότι στερείται α1-αδρενεργικών υποδοχέων. Διέγερση αποκτάται με εισαγωγή μέσω πλασμιδίου α1-αδρενεργικών υποδοχέων, άρα το ενδογενές σηματοδοτικό σύστημα είναι παρόν και λειτουργικό. Επιπρόσθετα, ανακαλύψαμε ότι τα κύτταρα A7r5 εκφράζουν ενδογενώς λειτουργικούς β-αδρενεργικούς υποδοχείς. Θέτουμε έτσι τα θεμέλια για μία σε βάθος διερεύνηση του τυχόν ρόλου των β-αδρενεργικών υποδοχέων στον έλεγχο του φαινοτύπου των αγγειακών ΛΜΚ, ο οποίος είναι καθοριστικός για την γένεση και πορεία των καρδιαγγειακών νοσημάτων εν γένει. Συμπερασματικά λοιπόν α) τα μεσεγχυματικά βλαστικά κύτταρα προερχόμενα από τη γέλη Wharton ανθρώπινου ομφάλιου λώρου αποτελούν κατάλληλο πρότυπο σύστημα διερεύνησης της ρύθμισης των μοριακών μηχανισμών που εμπλέκονται στη διαφοροποίηση προς ΛΜΚ από μόρια φαρμακολογικής σημασίας, και β) τα κύτταρα A7r5 αποτελούν καλό πρότυπο σύστημα για την διερεύνηση του τυχόν ρόλου των β-αδρενεργικών υποδοχέων στον έλεγχο του φαινοτύπου των ΛΜΚ των αγγείων. / The control of the genes that specify the Smooth Muscle Cell Phenotype is of great importance for our understanding, at a molecular level, of the processes central in a number of human pathologies. Among the diseases whose onset and progress is influenced by alterations in Smooth Muscle-Like (SM-L) phenotype are atherosclerosis, organ fibrosis (lung, liver and kidney), and metastasis associated with solid tumors. For these reasons, the understanding of the cell and molecular mechanisms that lead to changes in the SM phenotype expression are of central importance in our efforts to identify new approaches in limiting the progress of these diseases and the manifestation of the associated clinical symptoms. The first Aim of this work was the development and initial characterization of an in vitro model of differentiation towards a Smooth-Muscle-Like phenotype, to serve for the study of its molecular control. Initially, we characterized basic important molecular tools useful in determining the SM-L phenotype. With their aid, we developed and characterized a model system based on Wharton’s Jelly-derived Mesenchymal stem Cells (MSCs). In these cells, the expression of genes and proteins characteristic of the SM Phenotype depends on the protein levels of Serum Response Factor (SRF) and on the existence of SRF-binding elements on the promoters of the SM-specific genes; it is also potently induced by the exogenous expression of the transcription factor Myocardin. Therefore, this population of MSCs behaves as other characterized model systems, in that their differentiation to a SM-L phenotype is supported by the synergistic action of SRF and Myocardin. This novel model system based on Wharton’s Jelly MSCs will be useful to study the role of specific physiological and pharmacological agents in the control of the SM phenotype. In addition, such a system can offer insights in the basic cellular process of Epithelial-to-Mesenchymal Transition (EMT) and by extent, in the pathological mechanisms of diseases characterized by EMT. In parallel, we investigated whether the differentiated SMC line A7r5 is a viable pharmacological model system to investigate the control of the SMC phenotype by adrenergic receptors, a family of receptors that plays a crucial role in the homeostasis of the vessel wall. We showed that A7r5 cells do not express functional α1-adrenergic receptors; however, the intracellular signaling system linked to α-adrenergic receptors is present and functional. In contrast, A7r5 cells endogenously express functional β-adrenergic receptors, and A7r5 cells are therefore an attractive model to study the role of these receptors in the control of the SMC-phenotype. In conclusion, a) Mesenchymal Stem Cells from Wharton’s Jelly surrounding the human umbilical cord are a suitable in vitro model for the study of the molecular mechanisms that modulating Smooth Muscle Cell differentiation, and b) A7r5 cells are a good in vitro model system to investigate the role of the β-adrenergic receptor in controlling the phenotype of Vascular Smooth Muscle cells.

Le vieillissement s'accompagne d'une perte progressive de la masse et de la fonction musculaire, appelée sarcopénie. Différents mécanismes ont été proposés pour expliquer la sarcopénie. Cependant, la majorité d'entre eux ont été identifiés dans le contexte d'une atrophie induite expérimentalement (par dénervation, immobilisation, jeûne...) ou via des études corrélatives chez l'homme. Ainsi nous ne connaissons pas aujourd'hui l'importance et la chronologie de ces facteurs dans le contexte du vieillissement physiologique. Caenorhabditis elegans est un organisme modèle de référence pour les études de longévité. Grâce aux outils génétiques disponibles chez le nématode C. elegans, des voies moléculaires, qui contrôlent la longévité et dont le rôle est conservé chez les mammifères, ont pu être identifiées, comme la voie du récepteur de l'insuline/IGF-1. Toutefois le vieillissement musculaire a été très peu étudié dans cet organisme.Le premier objectif de mon projet de thèse était de décrire chez C. elegans les changements subcellulaires qui sont associés la perte de mobilité avec l'âge afin d'identifier des biomarqueurs potentiels du vieillissement musculaire. Le deuxième objectif était d'utiliser ces biomarqueurs comme outil pour identifier des gènes modificateurs de la sarcopénie. Nous avons ainsi pu mettre en évidence une diminution de l'expression de gènes impliqués dans la structure et la fonction musculaire très tôt au cours de la vie adulte. Ce phénotype est suivi par une fragmentation progressive des mitochondries puis une accumulation de vésicules d'autophagie. Ces biomarqueurs ont été utilisés pour tester le rôle potentiel, dans le maintien du muscle, de facteurs impliqués dans la différenciation musculaire au cours de l'embryogenèse.L'ensemble des résultats obtenus nous permettent de proposer un modèle selon lequel le facteur de transcription unc-120, orthologue du Serum Response Factor, agirait en aval de la voie de signalisation de l'insuline/IGF-1 dans le contrôle des différents biomarqueurs du vieillissement musculaires / Aging is accompanied by a progressive loss of muscle mass and function, named sarcopenia. Different mechanisms have been proposed to explain it. Furthermore most of them have been identified in the context of an experimental induced atrophy (by denervation, immobilization, fasting...) or via correlative studies in humans. Thus today we do not know the importance and chronology of these factors in the context of physiological aging. Caenorhabditis elegans is a reference model organism for longevity studies. Thanks to genetics tools available for the nematode C. elegans, evolutionarily conserved molecular pathways, which control longevity, have been identified, such as the Insulin/IGF-1 receptor pathway. However muscle aging has been very poorly studied in this organism. The first aim of my thesis project was to describe, in C. elegans, subcellular changes that are associated with mobility loss with age in order to determine potential biomarkers of muscle aging. The second aim was to use these biomarkers as tools to identify genes able to modify sarcopenia. Specifically, we could highlight a decrease of expression of genes involved in muscle mass and function very early during adulthood. This phenotype is followed by a gradual mitochondrial fragmentation then an accumulation of autophagic vesicles.These biomarkers have been used to test the potential role in muscle maintenance, of factors involved in muscle differentiation during embryogenesis. Altogether these results suggest a model in which the transcription factor unc-120, ortholog of Serum Response Factor, would act downstream in the insulin/IGF-1 signalization pathway on the control of the different biomarkers of muscle aging