Spelling suggestions: "subject:"abiogenesis"" "subject:"angogenesis""
161 |
Ultraestrutura do aparelho reprodutor feminino e mecanismos de transmissão transovariana de endossimbiontes de Diaphorina citri Kuwayama, 1908 (Hemiptera: Psyllidae) / Ultrastructure of the female reproductive system and mechanisms of transovarial transmission of endosymbionts of Diaphorina citri Kuwayama, 1908 (Hemiptera: Psyllidae)Fábio Cleisto Alda Dossi 30 January 2009 (has links)
Diaphorina citri Kuwayama, 1908 (Hemiptera: Psyllidae) tornou-se um psilídeo de grande importância para a citricultura paulista após a constatação da bactéria Candidatus Liberibacter sp., causadora do Huanglongbing (greening). Sabe-se que esse inseto abriga microrganismos endossimbiontes, os quais desempenham papel fundamental em sua ecologia nutricional, sendo transmitidos verticalmente à progênie. Dessa forma, propomos caracterizar a morfologia do aparelho reprodutor feminino durante o seu desenvolvimento para embasar a identificação do processo de migração dos simbiontes do bacterioma aos tecidos reprodutivos. D. citri possui ovário do tipo telotrófico, com ovaríolos organizados em bouquet e características gerais semelhantes às observadas para outros Sternorrhyncha. Os trofócitos parecem ser desprovidos de delimitação por membrana no ovaríolo desenvolvido. Um único oócito se desenvolve por ciclo no vitelário, o qual mantém-se em contato com a câmara trófica por um prolongamento citoplasmático, denominado cordão trófico. As informações morfo-estruturais do aparelho reprodutor de D. citri obtidas indicam similaridades importantes a de outros membros de Sternorryncha. Nesse contexto, a migração de simbiontes do bacterioma para os oócitos em maturação de D. citri, ocorre de modo semelhante ao descrito para aleirodídeos, caracterizandose pela migração de bacteriócito intacto. Este último, atravessa o epitélio de revestimento do oócito, formado por células foliculares, e invade o oócito, liberando as bactérias nele contidas. Entretanto, os simbiontes associados ao sincício do bacterioma, são liberados na hemocele através de uma pequena abertura formada no epitélio de revestimento dessa estrutura, invadindo o oócito por um mecanismo distinto. Os simbiontes contidos no oócito, formam um agrupamento de aspecto arredondado (= symbiont ball) na região posterior do oócito, próximo ao pedicelo. / Diaphorina citri Kuwayama, 1908 (Hemiptera: Psyllidae) became a serious problem to the citrus industry in São Paulo State once the Huanglongbing disease (greening), which is caused by the bacteria Candidatus Liberibacter sp., was detected. Psyllids are known to harbor endosymbiont microorganisms, which are vertically transmitted to the progeny and play a key role in the nutritional ecology of their hosts. Therefore, we aimed to characterize the morphology of the reproductive system during D. citri development as a tool for further investigation on the symbiont migration from the bacteriome to the reproductive tissues. D. citri has telotrophic ovaries with ovarioles organized in a bouquet, sharing all other characteristics with the remaining Sternorrhyncha. In developed ovarioles, trophocytes seems to lack any membrane delimitation. Only one oocyte develops at a time in the vitellarium, remaining in communication with the trophic chamber by a citoplasmatic brigde, named trophic cord. The morphostructural information reported in here on the D. citri reproductive system shows important similarities with other Sternorryncha. Symbionts associated to the bacteriome of D. citrus migrate to the ovaries and invade the oocytes during ovary maturation, as previously reported for aleyrodids. In this case, symbionts will move within the bacteriocyte as it detaches from the bacteriome and moves through the oocyte follicular epithelium, releasing the contained bacteria into the oocyte. However, symbionts associated to the bacteriome syncitium are relased into the hemocoel through small openings on the bacteriome epithelium, invading the oocyte by a different mechanism. All symbionts that invaded or were discharged into the oocyte aggregate into a balllike symbiont structure at the posterior pole close to the egg pedicel.
|
162 |
Contrôle de AP-1 sur le trafic de E-Cadhérine chez Drosophila melanogaster / AP-1 dependent E-Cadherin trafficking in Drosophila melanogasterLoyer, Nicolas 16 October 2014 (has links)
L'intérieur des cellules eucaryotes est compartimenté en organites qui échangent des lipides et protéines entre eux et avec la membrane plasmique via le trafic vésiculaire. Dans les cellules polarisées comme les cellules épithéliales, dont la membrane plasmique est divisée en un pôle apical et un pôle basolatéral séparés par une ceinture de jonctions, le trafic vésiculaire est contrôlé par des systèmes de tri polarisé, permettant d'adresser les protéines appropriées au domaine membranaire approprié. Dans ces cellules épithéliales, le complexe adaptateur AP-1 contrôle l'adressage au pôle basolatéral et le trafic de la molécule d'adhésion E-Cadhérine, une protéine transmembranaire des jonctions d'adhérence. Il a de plus été démontré dans les cellules intestinales du nématode C. elegans et des mammifères qu'AP-1 est nécessaire au maintien de la polarité épithélial. J'ai étudié ces fonctions d'AP-1 chez l'organisme modèle Drosophila melanogaster. J'ai montré qu'AP-1 contrôle aussi le trafic de E-Cadhérine chez la Drosophile mais n'est pas requis pour la maintenance de la polarité de l'épithélium folliculaire, un épithélium entourant le cyste germinal femelle de 16 cellules au cours de l'ovogénèse chez la Drosophile. Ces expériences dans ce tissu m'ont amené à découvrir une nouvelle fonction de E-Cadhérine dans le cyste germinal. Les cellules de ce cyste sont connectées entre elles par des ponts cytoplasmiques stabilisés à l'issue de cytocinèses incomplètes. J'ai montré que les cellules du cyste mutantes pour AP-1 présentent un phénotype de multinucléation dû au décrochage des ponts cytoplasmiques. Ce phénotype corrèle avec un défaut d'adressage de E-Cadhérine dépendant d'AP-1 à la membrane plasmique entourant ces ponts, via les endosomes de recyclage. E-Cadhérine y est nécessaire pour leur ancrage à la membrane plasmique, un rôle qui avait été jusque-Là masqué par l'expression ectopique compensatoire de N-Cadhérine dans les mutants E-Cadhérine. Ce rôle d'E-Cadhérine passe par l'organisation de protrusions membranaires présentant l'aspect et contenant certains marqueurs protéiques des microvillosités observées au pôle apical des cellules épithéliales. / Eukaryotic cells are compartmentalized in organelles. Lipidic and proteic exchanges between organelles and the plasma membrane are controlled by vesicular trafficking. In polarised cells such as epithelial cells, whose plasma membrane is divided into an apical and a basolateral pole separated by a junctional belt, appropriate targeting of proteins to appropriate poles relies on polarised sorting mechanisms controlling vesicular trafficking. In these cells, the clathrin adaptor complex AP-1 controls basolateral targeting and trafficking of the adhesion molecule E-Cadherin, a transmembrane adherens junctions protein. AP-1 is furthermore necessary for epithelial polarity maintenance in intestinal epithelial cells in the nematode C. elegans and mammals. I studied AP-1 functions in the model organism Drosophila melanogaster. I showed AP-1 also controls E-Cadherin trafficking in Drosophila but is not required for polarity maintenance in follicular cells, an epithelium surrounding the female germline cyst during oogenesis. Experiments in this tissue led me to discover a new E-Cadherin function in the germline cyst. Germline cyst cells are interconnected by cytoplasmic bridges stabilised after incomplete cytokinesis. I showed AP-1 mutant cyst cells were multinucleated due to a detachment of cytoplasmic bridges from the plasma membrane. This phenotype correlated with an E-Cadherin AP-1-Dependent targeting defect from recycling endosomes to the plasma membrane surrounding these bridges. E-Cadherin is necessary for their anchoring to the plasma membrane, a role that was hidden by ectopic compensatory expression of N-Cadherin in E-Cadherin mutants. This new role is mediated by E-Cadherin-Dependent organisation of membrane protrusions similar in aspect with and containing proteins of microvillosities present at the apical pole of epithelial cells.
|
163 |
GLS-1, a novel P granule component, modulates a network of conserved RNA regulators to influence germ cell fate decisionsEckmann, Christian R., Schmid, Mark, Kupinski, Adam P., Jedamzik, Britta, Harterink, Martin, Rybarska, Agata 26 November 2015 (has links)
Post-transcriptional regulatory mechanisms are widely used to influence cell fate decisions in germ cells, early embryos, and neurons. Many conserved cytoplasmic RNA regulatory proteins associate with each other and assemble on target mRNAs, forming ribonucleoprotein (RNP) complexes, to control the mRNAs translational output. How these RNA regulatory networks are orchestrated during development to regulate cell fate decisions remains elusive. We addressed this problem by focusing on Caenorhabditis elegans germline development, an exemplar of post-transcriptional control mechanisms. Here, we report the discovery of GLS-1, a new factor required for many aspects of germline development, including the oocyte cell fate in hermaphrodites and germline survival. We find that GLS-1 is a cytoplasmic protein that localizes in germ cells dynamically to germplasm (P) granules. Furthermore, its functions depend on its ability to form a protein complex with the RNA-binding Bicaudal-C ortholog GLD-3, a translational activator and P granule component important for similar germ cell fate decisions. Based on genetic epistasis experiments and in vitro competition experiments, we suggest that GLS-1 releases FBF/Pumilio from GLD-3 repression. This facilitates the sperm-to-oocyte switch, as liberated FBF represses the translation of mRNAs encoding spermatogenesis-promoting factors. Our proposed molecular mechanism is based on the GLS-1 protein acting as a molecular mimic of FBF/Pumilio. Furthermore, we suggest that a maternal GLS-1/GLD-3 complex in early embryos promotes the expression of mRNAs encoding germline survival factors. Our work identifies GLS-1 as a fundamental regulator of germline development. GLS-1 directs germ cell fate decisions by modulating the availability and activity of a single translational network component, GLD-3. Hence, the elucidation of the mechanisms underlying GLS-1 functions provides a new example of how conserved machinery can be developmentally manipulated to influence cell fate decisions and tissue development.
|
164 |
Understanding the Sequence-Specificity and RNA Target Recognition Properties of the Oocyte Maturation Factor, OMA-1, in Caenorhabditis elegans: A DissertationKaymak, Ebru 28 April 2016 (has links)
Maternally supplied mRNAs encode for necessary developmental regulators that pattern early embryos in many species until zygotic transcription is activated. In Caenorhabditis elegans, post-transcriptional regulatory mechanisms guide early development during embryogenesis. Maternal transcripts remain in a translationally silenced state until fertilization. A suite of RNA-binding proteins (RBP’s) regulate these maternally supplied mRNAs during oogenesis, the oocyte-to-embryo transition, and early embryogenesis. Identifying the target specificity of these RNA-binding proteins will reveal their contribution to patterning of the embryo. We are studying post-transcriptional regulation of maternal mRNAs during oocyte maturation, which is an essential part of meiosis that prepares oocytes for fertilization. Although the physiological events taking place during oocyte maturation have been well studied, the molecular mechanisms that regulate oocyte maturation are not well understood.
OMA-1 and OMA-2 are essential CCCH-type tandem zinc finger (TZF) RBP’s that function redundantly during oocyte maturation. This dissertation shows that I defined the RNA-binding specificity of OMA-1, and demonstrated that OMA-1/2 are required to repress the expression of 3ʹUTR reporters in developing oocytes. The recovered sequences from in vitro selection demonstrated that OMA-1 binds UAA and UAU repeats in a cooperative fashion. Interestingly, OMA-1 binds with high affinity to a conserved region of the glp-1 3ʹUTR that is rich in UAA and UAU repeats. Multiple RNA-binding proteins regulate translation of GLP-1 protein, a homolog of Notch receptor. In addition to previously identified RBP’s, we showed that OMA-1 and OMA-2 repress glp-1 reporter expression in C. elegans oocytes.
Mapping the OMA-1 dependent regulatory sites in the glp-1 mRNA and characterizing the interplay between OMA-1 and other factors will help reveal how multiple regulatory signals coordinate the transition from oocyte to embryo but the abundance of OMA-1 binding motifs within the glp-1 3ʹUTR makes it infeasible to identify sites with a functional consequence. I therefore first developed a strategy that allowed us to generate transgenic strains efficiently using a library adaptation of MosSCI transgenesis in combination with rapid RNAi screening to identify RBP-mRNA interactions with a functional consequence. This allowed me to identify five novel mRNA targets of OMA-1 with an in vivo regulatory connection. In conclusion, the findings in this dissertation provide new insights into OMA-1 mediated mRNA regulation and provide new tools for C. elegans transgenesis. Development of library MosSCI will advance functional mapping of OMA-1 dependent regulatory sites in the target mRNAs. Extending this strategy to map functional interactions between mRNA targets and RNAbinding proteins in will help reveal how multiple regulatory binding events coordinate complex cellular events such as oocyte to embryo transition and cell-fate specification.
|
165 |
Functional study of miRNA-mRNA interactions in malaria mosquito An. gambiaeFu, Xiaonan 02 July 2018 (has links)
Female adults of many mosquito species possess distinct physiological features adapting to blood feeding for successful reproduction. The disease pathogens that are transmitted by mosquitoes have evolved to take advantages of the indispensable blood feedings to complete their transmission cycles and to survive attacks from the mosquito's innate immune system. Normal egg development and mosquito immunity are tightly controlled by tissue- and stage-specific gene expression and coordinated by many signal molecules in the mosquito. Understanding gene regulation affecting mosquito reproduction and malaria parasites infection is of paramount importance for developing novel malaria control strategies. A growing body of evidence indicates that microRNAs (miRNAs) are involved in egg maturation and immune reactions against invading pathogens in mosquitoes. However, the molecular mechanisms by which specific miRNAs selectively modulate reproduction and the survival of pathogens are largely unknown.
The miRNA-induced gene-silencing pathway in mosquitoes was mostly extrapolated from the studies of flies. To explore the dynamics of miRNAs in reproduction, I used small RNAs sequencing to monitor miRNAs expression and their association with Argonaute 1 (Ago1) and Argonaute 2 (Ago2) in the malaria mosquito Anopheles gambiae (An. gambiae) during the 72-h period immediately after blood feeding. I found the abundance and Ago loading of most of the mature miRNAs were relatively stable after blood ingestion. However, miRNAs of the miR-309/286/2944 cluster were considerably upregulated after blood feeding. I confirmed that miR-309 is essential for normal egg development by depletion of endogenous miR-309 with a specific antagomir. In addition, my results showed that the Ago association of some miRNAs was not proportional to their cellular abundance implying additional regulation at miRNA integration.
To investigate the functional roles of miRNAs and define context-dependent miRNA-mRNA interactions during the reproductive process, I have applied an innovative experimental approach to study miRNA-mRNA interactome. CLEAR (covalent ligation of endogenous Argonaute-bound RNAs)-CLIP can generate miRNA-mRNA chimeras from UV-irradiation stabilized Ago-miRNA-mRNA complex. My results have defined tens of thousands of miRNA-mRNA interactions in mosquitoes, including novel targets for mosquito-specific miRNAs. Verification of the predicted interactions using mRNA-seq, ribosome-profiling, and luciferase reporter assay revealed a reliable miRNA-mRNA interaction network. Based on the detected interactions, I refined the paring rules for mosquito miRNAs and illustrated the dynamic pairing between different regions of miRNAs with their targets in vivo. The miRNA-mRNA interactions were compared using this approach at multiple time points before and after blood feeding. Importantly, this study showed that the interactions were dynamic and enriched in genes that are involved in metabolisms, supporting the proposed functions of miRNAs in coordinating the gene regulation in mosquito reproduction.
Plasmodium falciparum (P. falciparum) is a major human malaria parasite. To understand the functions of miRNAs in the mosquito resistance to Plasmodium infection, we analyzed the miRNA-mRNA interactions after female mosquitoes taking a P. falciparum-infected blood meal or an uninfected blood meal. Comparison of the interactions revealed enhanced miRNA-mRNA interactions after P. falciparum infection involving a group of immunity-related genes. In summary, this study has provided a systematic view and significantly advanced our understanding of the miRNA functions in mosquito reproduction and P. falciparum infection. / PHD
|
166 |
Reproduction sexuée et asexuée chez le poisson Chrosomus eos × eos-neogaeus : contexte, mécanismes et implicationsLafond, Joëlle 01 1900 (has links)
La reproduction est un processus essentiel à la persistance et à l’évolution des espèces. En ce sens, il existe une diversité incroyable de stratégies permettant la prolifération des individus. La reproduction sexuée typique, abondante chez les animaux, est très souvent la première qui vient à l’esprit. Cependant, chez les vertébrés, on retrouve plusieurs reproductions atypiques, où il est possible de manipuler la gamétogenèse de façon surprenante. Retrouvées surtout chez les hybrides, ces reproductions alternatives peuvent nous en apprendre long sur le fonctionnement de la méiose et de la gamétogenèse en général via l’étude de ses exceptions. Les projets réunis sous cette thèse ont ainsi pour objectif global d’apporter une meilleure description de ces reproductions atypiques avec une approche multidisciplinaire. À ce but, un complexe de vertébrés possédant plusieurs ploïdies, compositions génomiques et reproductions atypiques différentes a été choisi comme sujet d’étude. Le complexe d’hybrides sujet de cette thèse est ainsi celui de Chrosomus eos-neogaeus, un groupe de cyprinidés s’étendant des États-Unis au Canada, dans lequel on retrouve à la fois de la reproduction sexuée et asexuée. Plus précisément, ce projet de recherche cherche à décrire la façon dont se reproduisent les triploïdes hybrides Chrosomus eos × eos-neogaeus, le déterminisme derrière la dichotomie reproductive de ces derniers, ainsi que l’impact des reproductions sexuées et asexuées sur les organismes de ce complexe. Les différentes études réalisées ont permis de réaliser ce but, en accomplissant les 3 objectifs suivants. Le premier chapitre avait comme objectif la description des types de reproduction chez les hybrides triploïdes Chrosomus eos × eos-neogaeus à partir de croisements expérimentaux. Le second, d’inférer le déterminisme à la base des deux gamétogenèses (sexuée et asexuée) retrouvées chez les triploïdes via l’analyse de loci épigénétiques. Finalement, le troisième avait pour objectif de déterminer les effets de la sexualité et l’asexualité en l’absence de facteurs confondants, et ce, via une analyse en morphométrie. Ces différentes études auront mené, premièrement, à la découverte d’une nouvelle voie reproductive chez les vertébrés (hybridogenèse améiotique), retrouvée chez certaines femelles triploïdes, en plus de la reproduction sexuée déjà observée chez d’autres (hybridogenèse méiotique). Ensuite, l’origine de la dichotomie reproductive aura été corrélée à la ploïdie maternelle des triploïdes. Ainsi, une femelle diploïde donnera naissance à des triploïdes se reproduisant de façon asexuée, et ces dernières à des triploïdes se reproduisant de façon sexuée. Finalement, les analyses morphométriques chez les organismes sexués et asexués de ce complexe auront montré une différence de forme inhérente au type de gonades, et ce, en absence de facteurs confondants, qui est conservée même entre des individus de composition génomique différente. En prenant connaissance de ces informations, il est alors possible de mieux comprendre la flexibilité entourant la gamétogenèse chez les vertébrés, ainsi que les impacts de ces changements sur les organismes eux-mêmes et ceux qui les entourent. Cette thèse aura ainsi avancé les connaissances au niveau des reproductions atypiques dans le complexe C. eos-neogaeus, mais ces découvertes seront aussi d’une grande utilité pour les complexes similaires et pour l’étude des différentes stratégies reproductives retrouvées chez les vertébrés. / Reproduction is an essential process for the persistence and evolution of species. In this sense, there is an incredible diversity of strategies for the proliferation of individuals. Typical sexual reproduction, abundant in animals, is certainly the first that comes to mind. However, among vertebrates, various atypical reproductions can be found, where it is possible to manipulate gametogenesis in surprising ways. Mostly found in hybrids, these alternative reproductions can teach us a lot about the functioning of meiosis and gametogenesis in general through the study of their exceptions. The projects gathered under this thesis aim to provide a better description of these atypical reproductions with a multidisciplinary approach. In this regard, a complex of vertebrates with multiple ploidies, genomic compositions, and different atypical reproductions has been chosen as the subject of study. Indeed, the hybrid complex studied in this thesis is Chrosomus eos-neogaeus, a group of cyprinids extending from the United States to Canada, which exhibits both sexual and asexual reproduction. Specifically, this research project seeks to describe the reproductive context of triploid hybrids Chrosomus eos × eos-neogaeus, the determinism behind their reproductive dichotomy, and the impact that sexual and asexual reproduction can have on organisms in this complex. The various studies conducted have achieved these goals by accomplishing the following three specific objectives. The first chapter aimed to describe the types of reproduction in triploid hybrids Chrosomus eos × eos-neogaeus through experimental crossings. The second objective was to infer the determinism behind the two gametogenic pathways (sexual and asexual) found in triploids through the analysis of epigenetic loci. Finally, the third objective was to determine the effects of sexuality and asexuality in the absence of confounding factors through morphometric analysis. These different studies have led, firstly, to the discovery of a new reproductive pathway in vertebrates (ameiotic hybridogenesis), found in some triploid females, in addition to the sexual reproduction already observed in others (meiotic hybridogenesis). Next, the origin of reproductive dichotomy has been correlated with the maternal ploidy of triploids. Thus, a diploid female will give birth to triploids reproducing asexually, and these will give birth to triploids reproducing sexually. Finally, morphometric analyses of the sexual and asexual organisms in this complex have shown an inherent shape difference in the gonads, in the absence of confounding factors, which is preserved even among individuals of different genomic compositions. With this information, it will be possible to better understand the flexibility surrounding gametogenesis in vertebrates, as well as the impacts of these changes on the organisms themselves and those around them. This thesis has advanced knowledge in atypical reproductions in the C. eos-neogaeus complex, but this knowledge will also be of great utility for similar complexes and for the study of different reproductive strategies.
|
167 |
Identifizierung und funktionelle Charakterisierung neuer RNA-Transportfaktoren in der Xenopus laevis Oozyte / Identification and functional characterization of novel RNA transport factors in Xenopus laevis oocytesLöber, Jana 29 April 2008 (has links)
No description available.
|
168 |
Implication de l'endosome de recyclage dans la migration cellulaire in vivoAssaker, Gloria 08 1900 (has links)
Au cours de l’ovogenèse chez la mouche du vinaigre: Drosophila melanogaster, un groupe de cellules folliculaires appelées cellules de bord, migrent à travers les cellules nourricières pour atteindre l’ovocyte. Cet événement, nécessitant la transition épithélio- mésenchymateuse (TEM), la réorientation, puis l’arrêt, ressemble à la formation de métastases.
L’endocytose est un régulateur clé de plusieurs événements polarisés, y compris la migration cellulaire. En effet, différentes protéines impliquées dans la migration, comme les intégrines et les E-cadhérines (cadhérines épithéliales), sont régulées par transport à travers les endosomes. De même, l’endocytose restreint au front de migration l’activité des récepteurs tyrosine kinases (RTKs) qui guident les cellules de bord dans leur mouvement. Cependant les mécanismes moléculaires de cette restriction spatiale de l’activité des RTKs demeurent largement inconnus. Nous avons testé l’implication du trafic vésiculaire à travers la machinerie d’endocytose, dans la migration dirigée des cellules de bord, car ce système est facilement accessible pour l’expression de protéines et l’analyse de mutants.
Nous avons commencé par confirmer une observation précédente du rôle de l’endosome précoce dans la migration des cellules de bord. Ensuite, nous avons identifié l’endosome de recyclage (ER) comme un régulateur clé de cette migration. En effet, nous avons démontré que l’expression dans les cellules de bord d’une forme dominante négative de Rab11, la petite GTPase régulant le transport vésiculaire à travers l’ER, bloque la migration ou entraîne de sévères défauts de migration dans environ 80% des chambres d’œufs examinées. De plus, nous observons par immunofluorescence une relocalisation de l’activité des RTKs alors que d’autres protéines de migration ne sont pas affectées par Rab11 dominant négatif. Ce résultat a été par la suite confirmé par une interaction génétique entre Rab11 et les RTKs. D’autre part, nous avons montré que le complexe exocyste, un effecteur de Rab11, est impliqué dans la migration des cellules de bord. Nous avons trouvé par microscopie confocale en tissu fixé et par microscopie en temps réel que Sec15, un composant de ce complexe, est polarisé, de façon Rab11- dépendante, dans des vésicules qui s’accumulent au front de migration tout au long du mouvement des cellules de bord. De plus, la perte de l’activité de Sec15 perturbe à son tour la migration. Ainsi, toutes ces données démontrent le rôle fondamental d’un cycle d’endo- exocytose dans le maintien des RTKs actifs au niveau du front de migration des cellules de bord le long de leur mouvement. / During Drosophila melanogaster’s oogenesis, a cluster of folllicle cells, called border cells, perform an invasive migration through the surrounding nurse cells to reach the oocyte. This event resembles metastasis formation since it requires epithelial- mesenchymal transition, reorientation and arrest.
Endocytosis plays a fundamental role in many polarized processes, including cell migration, since different migration proteins, like integrins and E-cadherins traffic through the endocytic pathway. Furthermore, receptor tyrosine kinases (RTKs) that guide border cells during their migration are regulated by endocytosis, although the mechanisms involved are largely unknown. We tested the implication of vesicular trafficking through the endocytic machinery, in border cells’ directed migration, because this system is easily accessible for protein expression and mutant analysis.
We first confirmed previous observation that trafficking through the early endosome is necessary for border cells migration, and then we identified the recycling endosome as a key compartment for this migration. Indeed, we showed that overexpression in border cells of a dominant negative form of Rab11, the small GTPase regulating vesicular trafficking through the recycling endosome, blocks migration or leads to severe migration defects in about 80% of examined egg chambers. Furthermore, using immunofluorescence, we observed a relocalization of RTKs activity, whereas other migration proteins were not redistributed upon dominant negative Rab11 expression. This result was further confirmed by a genetic interaction between Rab11 and RTKs. Moreover, we showed that the exocyst complex, an effector of Rab11, is also involved in border cells migration. We found by using confocal microscopy of fixed tissues and time-lapse microscopy of living egg chambers, that Sec15, a member of this complex, is distributed in vesicles which are polarized, in a Rab11- dependent manner, throughout border cells migration. In addition, loss of Sec15 also impairs migration. Together these data demonstrate a fundamental role for an endo- exocytic cycle in the maintenance of active RTKs at the leading edge of border cells during their migration.
|
169 |
Souffle/Spastizin regulates secretory granule maturation by sorting lysosomal cargo from immature secretory granule during zebrafish oogenesisPalsamy, Kanagaraj 18 November 2014 (has links)
No description available.
|
170 |
Implication de l'endosome de recyclage dans la migration cellulaire in vivoAssaker, Gloria 08 1900 (has links)
Au cours de l’ovogenèse chez la mouche du vinaigre: Drosophila melanogaster, un groupe de cellules folliculaires appelées cellules de bord, migrent à travers les cellules nourricières pour atteindre l’ovocyte. Cet événement, nécessitant la transition épithélio- mésenchymateuse (TEM), la réorientation, puis l’arrêt, ressemble à la formation de métastases.
L’endocytose est un régulateur clé de plusieurs événements polarisés, y compris la migration cellulaire. En effet, différentes protéines impliquées dans la migration, comme les intégrines et les E-cadhérines (cadhérines épithéliales), sont régulées par transport à travers les endosomes. De même, l’endocytose restreint au front de migration l’activité des récepteurs tyrosine kinases (RTKs) qui guident les cellules de bord dans leur mouvement. Cependant les mécanismes moléculaires de cette restriction spatiale de l’activité des RTKs demeurent largement inconnus. Nous avons testé l’implication du trafic vésiculaire à travers la machinerie d’endocytose, dans la migration dirigée des cellules de bord, car ce système est facilement accessible pour l’expression de protéines et l’analyse de mutants.
Nous avons commencé par confirmer une observation précédente du rôle de l’endosome précoce dans la migration des cellules de bord. Ensuite, nous avons identifié l’endosome de recyclage (ER) comme un régulateur clé de cette migration. En effet, nous avons démontré que l’expression dans les cellules de bord d’une forme dominante négative de Rab11, la petite GTPase régulant le transport vésiculaire à travers l’ER, bloque la migration ou entraîne de sévères défauts de migration dans environ 80% des chambres d’œufs examinées. De plus, nous observons par immunofluorescence une relocalisation de l’activité des RTKs alors que d’autres protéines de migration ne sont pas affectées par Rab11 dominant négatif. Ce résultat a été par la suite confirmé par une interaction génétique entre Rab11 et les RTKs. D’autre part, nous avons montré que le complexe exocyste, un effecteur de Rab11, est impliqué dans la migration des cellules de bord. Nous avons trouvé par microscopie confocale en tissu fixé et par microscopie en temps réel que Sec15, un composant de ce complexe, est polarisé, de façon Rab11- dépendante, dans des vésicules qui s’accumulent au front de migration tout au long du mouvement des cellules de bord. De plus, la perte de l’activité de Sec15 perturbe à son tour la migration. Ainsi, toutes ces données démontrent le rôle fondamental d’un cycle d’endo- exocytose dans le maintien des RTKs actifs au niveau du front de migration des cellules de bord le long de leur mouvement. / During Drosophila melanogaster’s oogenesis, a cluster of folllicle cells, called border cells, perform an invasive migration through the surrounding nurse cells to reach the oocyte. This event resembles metastasis formation since it requires epithelial- mesenchymal transition, reorientation and arrest.
Endocytosis plays a fundamental role in many polarized processes, including cell migration, since different migration proteins, like integrins and E-cadherins traffic through the endocytic pathway. Furthermore, receptor tyrosine kinases (RTKs) that guide border cells during their migration are regulated by endocytosis, although the mechanisms involved are largely unknown. We tested the implication of vesicular trafficking through the endocytic machinery, in border cells’ directed migration, because this system is easily accessible for protein expression and mutant analysis.
We first confirmed previous observation that trafficking through the early endosome is necessary for border cells migration, and then we identified the recycling endosome as a key compartment for this migration. Indeed, we showed that overexpression in border cells of a dominant negative form of Rab11, the small GTPase regulating vesicular trafficking through the recycling endosome, blocks migration or leads to severe migration defects in about 80% of examined egg chambers. Furthermore, using immunofluorescence, we observed a relocalization of RTKs activity, whereas other migration proteins were not redistributed upon dominant negative Rab11 expression. This result was further confirmed by a genetic interaction between Rab11 and RTKs. Moreover, we showed that the exocyst complex, an effector of Rab11, is also involved in border cells migration. We found by using confocal microscopy of fixed tissues and time-lapse microscopy of living egg chambers, that Sec15, a member of this complex, is distributed in vesicles which are polarized, in a Rab11- dependent manner, throughout border cells migration. In addition, loss of Sec15 also impairs migration. Together these data demonstrate a fundamental role for an endo- exocytic cycle in the maintenance of active RTKs at the leading edge of border cells during their migration.
|
Page generated in 0.0796 seconds